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        <title>Neurological Sciences via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Neurological Sciences' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Neurological+Sciences&t=Neurological+Sciences&s=Search&f=source]]></link>
        <lastBuildDate>Wed, 17 Mar 2010 14:52:20 +0100</lastBuildDate>
        <item>
            <title>Cognitive dysfunction in a patient with brainstem hemorrhage</title>
            <link>http://www.medworm.com/index.php?rid=3368064&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3401137gt0717182%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 54-year-old, right-handed male suffered sudden onset of vertigo and vomiting. He was diagnosed with brainstem hemorrhage,
 and treatment was administered. After the vertigo improved, he showed disturbance of attention and anterograde amnesia. Magnetic
 resonance imaging revealed a hematoma across the pons on both sides, but no lesions were obvious in the cerebellum or the
 cerebrum. Single photon emission tomography showed decreased perfusion not only in the brainstem but also in the bilateral
 frontal and temporal lobes. Amnesia and executive dysfunction decreased in the 8&amp;nbsp;months following the stroke onset, with improvement
 in regional cerebral blood flow to the frontal and temporal lobes. These findings suggest that a hemorrhage in the pons caused
 diaschisis ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3368064</comments>
            <pubDate>Sun, 14 Mar 2010 11:29:24 +0100</pubDate>
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        <item>
            <title>Adult dermatomyositis with severe polyneuropathy: does neuromyositis exist?</title>
            <link>http://www.medworm.com/index.php?rid=3368065&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa3572867l357323j%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Peripheral nerve involvement in dermatomyositis (DM) has been known as neuromyositis. However, the pathogenic mechanism is
 not clear, and the association between DM and peripheral neuropathy is still controversial. Our patient exhibited symptomatic
 polyneuropathy that was documented electrophysiologically in addition to typical features of DM. The sural nerve biopsy showed
 evidence of a continuing neuropathic process of axonal type. There was no finding of inflammatory cells infiltrating the vessels.
 Neither methylprednisolone nor intravenous immunoglobulin (IVIg) improved neurological symptoms including muscle weakness
 and sensory disturbance. Clinical, electrophysiological, and neuropathological features in our case demonstrate the association
 of DM and polyneur...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3368065</comments>
            <pubDate>Sun, 14 Mar 2010 11:29:22 +0100</pubDate>
            <guid isPermaLink="false">3368065</guid>        </item>
        <item>
            <title>Systemic thrombolysis with recombinant tissue plasminogen activator in acute ischemic stroke: first Croatian experiences</title>
            <link>http://www.medworm.com/index.php?rid=3368066&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9736713168jp13u2%2F</link>
            <description>We present a 2-year experience of thrombolytic therapy (2006–2008) in the stroke unit
 of the University Hospital in Zagreb, Croatian largest hospital, serving nearly one-fifth of the citizens of Croatia. Obtained
 data (vitals at admission and before administration of rt-PA; NIHSS and MRS scores at admission, 2&amp;nbsp;h and 7th day after rt-PA
 treatment, “time to door” and “door to needle” intervals, duration of hospital treatment as well as outcomes and complications
 of our 66 thrombolysed patients) are presented and discussed. We also present our results regarding benefits of this therapy
 as well as possible reasons for complications noticed.
 
 
	Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s10072-010-0237-1Authors
		Vesna Matijević, University Hospital ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3368066</comments>
            <pubDate>Sun, 14 Mar 2010 11:29:21 +0100</pubDate>
            <guid isPermaLink="false">3368066</guid>        </item>
        <item>
            <title>Recent developments in innervation imaging using iodine-123-metaiodobenzylguanidine scintigraphy in Lewy body diseases</title>
            <link>http://www.medworm.com/index.php?rid=3361029&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb2m31l31750610t2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Radiolabeled metaiodobenzylguanidine (MIBG) is an analog of guanethidine and is taken up by the postganglionic presynaptic
 nerve endings. MIBG uptake in the heart correlates with adrenergic function, which can be reduced in Lewy body diseases. We
 described the recent developments in innervation imaging using 123I-MIBG scintigraphy in Lewy body diseases including Parkinson’s disease and dementia with Lewy bodies. Particularly, we underlined
 the role of MIBG scintigraphy in differential diagnosis of movement disorders. As described by recent studies, MIBG scintigraphy
 is a valuable diagnostic tool for differentiation between Lewy body diseases and parkinsonian syndromes or other movement
 disorders with parkinsonism. Furthermore, this method may provide a powerful d...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3361029</comments>
            <pubDate>Thu, 11 Mar 2010 02:49:50 +0100</pubDate>
            <guid isPermaLink="false">3361029</guid>        </item>
        <item>
            <title>Parkinson’s disease: oxidative stress and therapeutic approaches</title>
            <link>http://www.medworm.com/index.php?rid=3361030&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa6123734256r416l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Parkinson’s disease (PD) is a neurodegenerative disorder, caused by reduced levels of catecholamines and oxidative stress.
 Symptoms seen in the disease include tremor, rigidity, bradykinesia and postural disability. Oxidative stress plays a key
 role in neurodegeneration and motor abnormalities seen in PD. Altered levels of the protein caused by these changes lead to
 defective ubiquitin–proteasome pathway. Neurodegeneration seen in PD and Canavan disease has a common mechanism. Recent studies
 suggest that herbal medicines can improve molecular changes and motor functions seen in PD.
 
 
	Content Type Journal ArticleCategory Review ArticleDOI 10.1007/s10072-010-0245-1Authors
		Sankar Surendran, LSUHSC School of Medicine New Orleans LA 70112 USASrinivasagam Rajasan...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3361030</comments>
            <pubDate>Thu, 11 Mar 2010 02:49:49 +0100</pubDate>
            <guid isPermaLink="false">3361030</guid>        </item>
        <item>
            <title>Recognition and naming of famous buildings: Italian normative data</title>
            <link>http://www.medworm.com/index.php?rid=3356448&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw363118724058n88%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Semantically unique items are concrete entities characterized by a unique cluster of semantic information. In this field,
 neuropsychology has always given more attention to faces than to other kind of stimuli. An important category that has been
 largely neglected so far is famous buildings. A total of 200 healthy Italian adults with age, sex and education homogenously
 distributed across subgroups were administered a famous buildings naming and recognition test, which assessed both visual
 and verbal modalities. The test was divided in seven sections; norms were calculated taking into account demographic variables
 such as age, sex and education. Multiple regression analyses showed that education influenced significantly the performance
 on all subtests; age had a sig...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3356448</comments>
            <pubDate>Wed, 10 Mar 2010 15:26:52 +0100</pubDate>
            <guid isPermaLink="false">3356448</guid>        </item>
        <item>
            <title>Presenilin 1 gene mutation (M139I) in a patient with an early-onset Alzheimer’s disease: clinical characteristics and genetic identification</title>
            <link>http://www.medworm.com/index.php?rid=3356452&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb17056x066081q7g%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Mutations in the presenilin 1 (PSEN1) gene are more commonly identified as genetic causes of early-onset familial Alzheimer’s disease than mutations in the amyloid
 precursor protein (APP) and the presenilin 2 (PSEN2) genes. More than 100 different mutations in the PSEN1 gene have been detected, and the clinical phenotypes have been described in the literature. This paper reports the case of
 a 38-year-old female showing early memory impairment and having a base pair mutation from guanine (G) to cytosine (C) at codon
 139 of PSEN1, which leads to the substitution of a methionine with an isoleucine.
 
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-010-0233-5Authors
		Hee-Jin Kim, Hanyang University Department of Neurology, College of Medicine 17 ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3356452</comments>
            <pubDate>Wed, 10 Mar 2010 15:26:49 +0100</pubDate>
            <guid isPermaLink="false">3356452</guid>        </item>
        <item>
            <title>“Dropping objects”: a potential index of severe carpal tunnel syndrome</title>
            <link>http://www.medworm.com/index.php?rid=3356451&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu7648052602pl2p1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Patients affected by carpal tunnel syndrome (CTS) often report finding themselves “dropping objects”. This symptom is perceived
 as a severe and frustrating problem. We investigated the occurrence of “dropping objects” in a sample of 532 patients affected
 by CTS, studied with a multidimensional protocol (clinical, neurophysiological, and patient-oriented). To ensure that the
 definition of “dropping objects” was index of abnormality, we evaluated a control group interviewing 200 subjects. In order
 to evaluate if “dropping objects” was an index of more severe CTS impairment, we compared the severity measures between the
 patients with and without this condition. Severity of CTS multidimensionally assessed was significantly greater in patients
 with a hi...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3356451</comments>
            <pubDate>Wed, 10 Mar 2010 15:26:49 +0100</pubDate>
            <guid isPermaLink="false">3356451</guid>        </item>
        <item>
            <title>The enhancement effect of beta-boswellic acid on hippocampal neurites outgrowth and branching (an in vitro study)</title>
            <link>http://www.medworm.com/index.php?rid=3356450&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4887311245229407%2F</link>
            <description>In this study, the effect
 of BBA was examined on neurites outgrowth and branching as well as on polymerization dynamics of tubulin. The morphometric
 parameters (axonal length and neuritis branching) were examined microscopically after treating the hippocampal cells with
 BBA. Also the assembly process of tubulin was assessed using UV/V is spectrophotometer through following of absorbance at
 350&amp;nbsp;nm. The results revealed that BBA could significantly enhance neurite outgrowth, branching, and tubulin polymerization
 dynamics. The obtained results suggest that enhancing effect of BBA on microtubule polymerization kinetics might be the origin
 of increasing axonal outgrowth and branching.
 
 
	Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s10072-010-0220-xAuthors
		Ove...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3356450</comments>
            <pubDate>Wed, 10 Mar 2010 15:26:49 +0100</pubDate>
            <guid isPermaLink="false">3356450</guid>        </item>
        <item>
            <title>Effects of blockade of ionotropic glutamate receptors on blood–brain barrier disruption in focal cerebral ischemia</title>
            <link>http://www.medworm.com/index.php?rid=3356449&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc621v2wtq83q0m38%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To determine whether blockade of ionotropic glutamate receptors such as NMDA or AMPA receptors would attenuate blood–brain
 barrier (BBB) disruption in focal cerebral ischemia, 15&amp;nbsp;min before middle cerebral artery (MCA) occlusion, CGS-19755 or NBQX
 was injected intraperitoneally in rats. At 1&amp;nbsp;h after MCA occlusion, BBB permeability was determined by measuring the transfer
 coefficient (K
 
 i
 ) of 14C-α-aminoisobutyric acid and the volume of dextran distribution. With MCA occlusion, K
 
 i
 was increased in the ischemic cortex (IC) (316%). CGS-19755 attenuated the increase in K
 
 i
 in the IC (−46%), but NBQX did not significantly decrease it. The difference in the volume of dextran distribution between
 the IC and the contralateral cortex became insig...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3356449</comments>
            <pubDate>Wed, 10 Mar 2010 15:26:49 +0100</pubDate>
            <guid isPermaLink="false">3356449</guid>        </item>
        <item>
            <title>Apoplexy in the everyday practice in the eighteenth century</title>
            <link>http://www.medworm.com/index.php?rid=3356453&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F336lk07173075820%2F</link>
            <description>We report the original recipes applied to treat apoplexy in the eighteenth century, as written in the personal notes of doctor
 of that century.
 
 
	Content Type Journal ArticleCategory Brief CommunicationDOI 10.1007/s10072-010-0223-7Authors
		Biagio Arnone, Clinic Center, Private Hospital for Rehabilitation Naples ItalyClaudio Crisci, Clinic Center, Private Hospital for Rehabilitation Naples Italy
	

	
		Journal Neurological SciencesOnline ISSN 1590-3478Print ISSN 1590-1874 (Source: Neurological Sciences)</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3356453</comments>
            <pubDate>Wed, 10 Mar 2010 15:26:48 +0100</pubDate>
            <guid isPermaLink="false">3356453</guid>        </item>
        <item>
            <title>A case of idiopathic low CSF pressure headache presenting as cough headache</title>
            <link>http://www.medworm.com/index.php?rid=3356454&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa43u6t53363315xk%2F</link>
            <description>We report the case of an idiopathic low CSF pressure presenting as a
 cough headache.
 
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-010-0240-6Authors
		Angelo Nuti, Hospital of Viareggio Neurology Unit Lido di Camaiore LU ItalyFilippo Baldacci, University of Pisa Neurosciences Department Pisa ItalyClaudio Lucetti, Hospital of Viareggio Neurology Unit Lido di Camaiore LU ItalyCristina Dolciotti, Hospital of Viareggio Neurology Unit Lido di Camaiore LU ItalyGabriele Cipriani, Hospital of Viareggio Neurology Unit Lido di Camaiore LU ItalyUbaldo Bonuccelli, University of Pisa Neurosciences Department Pisa Italy
	

	
		Journal Neurological SciencesOnline ISSN 1590-3478Print ISSN 1590-1874 (Source: Neurological Sciences)</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3356454</comments>
            <pubDate>Wed, 10 Mar 2010 15:26:46 +0100</pubDate>
            <guid isPermaLink="false">3356454</guid>        </item>
        <item>
            <title>Minocycline with aspirin: a therapeutic approach in the treatment of diabetic neuropathy</title>
            <link>http://www.medworm.com/index.php?rid=3356456&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fhk1n48q402j85231%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Enhanced production of matrix metalloproteinase-2 (MMP-2) and matrix metalloproteinase-9 (MMP-9) in diabetes leads to degradation
 of extracellular matrix in blood vessels and leads to complications of diabetes. In the present study, we have targeted MMP-2
 and MMP-9 overactivation in diabetic neuropathy using a known MMP-2 and MMP-9 inhibitor, minocycline, with a non-selective
 COX inhibitor, aspirin. Streptozotocin-induced diabetic neuropathy was carried out in male Wistar rats and monitored by measuring
 the sensory nerve conduction velocity (SNCV), motor nerve conduction velocity (MNCV), tail flick latency and hot plate latency.
 Three weeks of treatment with a combination of minocycline and aspirin showed significant improvement in SNCV, MNCV, hot plate
 latency an...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3356456</comments>
            <pubDate>Wed, 10 Mar 2010 15:26:45 +0100</pubDate>
            <guid isPermaLink="false">3356456</guid>        </item>
        <item>
            <title>Cytokine polymorphisms and Alzheimer disease: possible associations</title>
            <link>http://www.medworm.com/index.php?rid=3356455&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr0u810548132h354%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Alzheimer’s disease (AD) is a degenerative dementia characterized by typical, destructive alterations of neurons (neurofibrillary
 tangles and amyloid plaques), and glial proliferation. Cytokine-driven inflammatory environment can contribute to the pathogenesis
 and/or progression of the disease. The aim of the study was to evaluate and compare genotypic and allelic polymorphisms of
 13 cytokine genes in 19 Caucasoid AD patients with medium–high level of dementia (assessed by an MMSE&amp;nbsp;&amp;lt;&amp;nbsp;24) and 20 normal
 controls affected by non inflammatory neuropsychiatric disease. Polymorphisms in the genes of IL-lA, IL-lB, IL-2, IL-4, IL-6,
 IL-10, IL-12, IFN-G, TGF-β, TNF-α, and of the cytokine receptors IL-lR, IL-IRA, IL-4RA were investigated. APO-E and ACE gene...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3356455</comments>
            <pubDate>Wed, 10 Mar 2010 15:26:45 +0100</pubDate>
            <guid isPermaLink="false">3356455</guid>        </item>
        <item>
            <title>Acute multiple cranial neuropathy in a patient with neurosarcoidosis</title>
            <link>http://www.medworm.com/index.php?rid=3336938&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6787561p06v63243%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorDOI 10.1007/s10072-010-0235-3Authors
		Sevda Erer-Ozbek, Uludag University School of Medicine Department of Neurology 16059 Bursa TurkeyIbrahim Bora, Uludag University School of Medicine Department of Neurology 16059 Bursa TurkeySukran Yurtogullar, Uludag University School of Medicine Department of Neurology 16059 Bursa Turkey
	

	
		Journal Neurological SciencesOnline ISSN 1590-3478Print ISSN 1590-1874 (Source: Neurological Sciences)</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3336938</comments>
            <pubDate>Wed, 03 Mar 2010 08:51:38 +0100</pubDate>
            <guid isPermaLink="false">3336938</guid>        </item>
        <item>
            <title>Tolosa–Hunt syndrome with reversible dissection aneurysm</title>
            <link>http://www.medworm.com/index.php?rid=3336941&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flm6714r5w8437783%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 49-year-old female presented with recurrent intolerable right retro-orbital pain, ptosis and diplopia for 4&amp;nbsp;months. Neurological
 evaluation revealed right oculomotor nerve and abducent nerve injuries. Neuroimaging found enlarged right cavernous sinus,
 right intracavernous carotid dissection aneurysm and a stenosis proximal to it. Tolosa–Hunt syndrome (THS) was suggested and
 treated with steroid. The clinical symptoms were alleviated after the treatment. After 3&amp;nbsp;months of follow-up cerebral angiography
 showed the lesions of the right intracavernous carotid stenosis and the dissection almost disappeared. Therefore, we proposed
 that the dissection and the stenosis are directly induced by the inflammation of THS.
 
 
	Content Type Journal ArticleCategory ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3336941</comments>
            <pubDate>Wed, 03 Mar 2010 08:51:36 +0100</pubDate>
            <guid isPermaLink="false">3336941</guid>        </item>
        <item>
            <title>Magnetic resonance imaging of pachymeningeal enhancement in Vogt-Koyanagi-Harada disease</title>
            <link>http://www.medworm.com/index.php?rid=3336940&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fvx4367834074010n%2F</link>
            <description>We report a case of VKH disease with panuveitis and
 meningeal involvement of the anterior temporal lobe detected by brain MRI.
 
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-010-0236-2Authors
		Hyun Jeong Han, Kwandong University Department of Neurology, College of Medicine, Myongji Hospital 697-24 Hawjeong-dong, Deukyang-gu, Goyang-shi Gyeonggi-do KoreaHye Yun Kim, Kwandong University Department of Neurology, College of Medicine, Myongji Hospital 697-24 Hawjeong-dong, Deukyang-gu, Goyang-shi Gyeonggi-do KoreaJong-Ho Park, Kwandong University Department of Neurology, College of Medicine, Myongji Hospital 697-24 Hawjeong-dong, Deukyang-gu, Goyang-shi Gyeonggi-do KoreaEun Ja Lee, Kwandong University Department of Radiology, College of Medicine, Myongji Hospital Gyeo...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3336940</comments>
            <pubDate>Wed, 03 Mar 2010 08:51:36 +0100</pubDate>
            <guid isPermaLink="false">3336940</guid>        </item>
        <item>
            <title>Hemangiopericytoma: collision with meningioma and recurrence</title>
            <link>http://www.medworm.com/index.php?rid=3336939&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F516887k7g7352457%2F</link>
            <description>This report
 provides the first documentation in the literature of a hemangiopericytoma colliding with a meningioma, and recurring after
 treatment with gross total resection. Surgical samples were fully evaluated with hematoxylin and eosin and reticulin staining,
 as well as immunohistochemical analysis. Results were classically representative of a hemangiopericytoma (World Health Organization
 grade II) and of a meningioma (World Health Organization grade I). This report of a unique collision tumor not only augments
 the repertoire of collision tumor combinations described in literature but also provides follow-up on the clinical outcome
 of the patient, thereby raising clinically relevant issues ranging from presentation to treatment paradigms.
 
 
	Content Type Journal ArticleCategory ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3336939</comments>
            <pubDate>Wed, 03 Mar 2010 08:51:36 +0100</pubDate>
            <guid isPermaLink="false">3336939</guid>        </item>
        <item>
            <title>Analysis of association between bleomycin hydrolase and apolipoprotein E polymorphism in Alzheimer’s disease</title>
            <link>http://www.medworm.com/index.php?rid=3336942&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4717gx22mr2w5j06%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Alzheimer’s disease (AD) is the leading cause of dementia. Several studies indicate a possible relationship between different
 genes and Alzheimer’s disease. To further investigate, we have analyzed the association between the bleomycin hydrolase (BLMH)
 and apolipoprotein E (ApoE) polymorphisms in 93 AD patients and age- and sex-matched 113 controls from the Tunisian population.
 The frequency of ApoE epsilon 4 allele was found to differ significantly in AD patients compared to the control [29.5% vs.
 8.8 (χ
 2&amp;nbsp;=&amp;nbsp;26, df&amp;nbsp;=&amp;nbsp;1, p&amp;nbsp;&amp;lt;&amp;nbsp;0.001)] leading to an increased risk of AD in subjects with this allele (OR&amp;nbsp;=&amp;nbsp;3.29, 95% CI&amp;nbsp;=&amp;nbsp;1.7–6.5; p&amp;nbsp;=&amp;nbsp;0.001]. This risk was found to decrease from OR&amp;nbsp;=&amp;nbsp;8.4, CI&amp;...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3336942</comments>
            <pubDate>Wed, 03 Mar 2010 08:51:35 +0100</pubDate>
            <guid isPermaLink="false">3336942</guid>        </item>
        <item>
            <title>Resection of the nerves bundle from the sphenopalatine ganglia tend to increase the infarction volume following middle cerebral artery occlusion</title>
            <link>http://www.medworm.com/index.php?rid=3336943&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F34884150612874l1%2F</link>
            <description>This study was aimed to investigate the effects of resection of the nerves
 bundle from the SPG of rat on the brain lesions following middle cerebral artery occlusion (MCAO), and evaluated the roles
 of the nitric oxygen synthase (NOS) immunoreactive perivascular nerves of cerebral arteries in MCAO. We found that 7&amp;nbsp;days
 after bilateral resections of the nerves bundle from the SPG, the NOS activity perivascular nerves in the middle cerebral
 arteries disappeared, and the infarction volume and the TUNEL positive cells increased significantly after 24&amp;nbsp;h MCAO, which
 implicated that the NOS contained nerves from the SPG maybe have an important role in the MCAO.
 
 
	Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s10072-010-0238-0Authors
		Su Diansan, Shanghai Jiaot...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3336943</comments>
            <pubDate>Wed, 03 Mar 2010 08:51:33 +0100</pubDate>
            <guid isPermaLink="false">3336943</guid>        </item>
        <item>
            <title>Is idiopathic intracranial hypertension without papilledema a risk factor for migraine progression?</title>
            <link>http://www.medworm.com/index.php?rid=3313235&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F675258263w1p5786%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The association of chronic migraine (CM) with an idiopathic intracranial hypertension without papilledema (IIHWOP), although
 much more prevalent than expected in clinical series of CM sufferers, is not included among the risk factors for migraine
 progression. We discuss the available evidence supporting the existence of a pathogenetic link between CM and idiopathic intracranial
 hypertensive disorders and suggest a causative role for IIHWOP in migraine progression.
 
 
	Content Type Journal ArticleCategory Review ArticleDOI 10.1007/s10072-010-0229-1Authors
		Roberto De Simone, University of Naples “Federico II” Headache Centre, Department of Neurological Sciences via Pansini, 5 80131 Naples ItalyAngelo Ranieri, University of Naples “Federico II” Headache Centr...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3313235</comments>
            <pubDate>Thu, 25 Feb 2010 06:54:37 +0100</pubDate>
            <guid isPermaLink="false">3313235</guid>        </item>
        <item>
            <title>Are subjective cognitive complaints a risk factor for dementia?</title>
            <link>http://www.medworm.com/index.php?rid=3313234&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe26661276h543449%2F</link>
            <description>The objective is to evaluate the prognosis of subjective cognitive complaints (SCC) patients during 4-year follow-up. A prospective
 study on 92 SCC patients investigating their cognitive, affective and behavioural aspects. SCC patients were classified as
 having no objective cognitive impairment (NOCI), mild cognitive impairment (MCI), or subtypes of MCI. Results: 43 patients
 were found to have NOCI and 49 MCI. During the follow-up, 45.5% of NOCI patients remained unchanged, 13.9% were diagnosed
 as MCI and only one progressed to dementia. Of the MCI patients, 32.3% remained stable, 18.4% became demented and 4% reverted
 to NOCI. Visual attention, behavioural memory, long-term verbal memory, apathy and caregiver distress, provided independent
 predictors of progression to dementia.
 
 
	...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3313234</comments>
            <pubDate>Thu, 25 Feb 2010 06:54:37 +0100</pubDate>
            <guid isPermaLink="false">3313234</guid>        </item>
        <item>
            <title>Three-dimensional motion analysis of the effects of auditory cueing on gait pattern in patients with Parkinson’s disease: a preliminary investigation</title>
            <link>http://www.medworm.com/index.php?rid=3313233&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fnh4t24386nx17272%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Auditory cueing enhances gait in parkinsonian patients. Our aim was to evaluate its effects on spatiotemporal (stride length,
 stride time, cadence, gait speed, single and double support duration) kinematic (range of amplitude of the hip, knee and ankle
 joint angles registered in the sagittal plane) and kinetic (maximal values of the hip and ankle joint power) gait parameters
 using three-dimensional motion analysis. Eight parkinsonian patients performed 12 walking tests: 3 repetitions of 4 conditions
 (normal walking, 90, 100, and 110% of the mean cadence at preferred pace cued walking). Subjects were asked to uniform their
 cadence to the cueing rhythm. In the presence of auditory cues stride length, cadence, gait speed and ratio single/double
 support duration incre...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3313233</comments>
            <pubDate>Thu, 25 Feb 2010 06:54:37 +0100</pubDate>
            <guid isPermaLink="false">3313233</guid>        </item>
        <item>
            <title>A case of secondary syphilis presenting as optic neuritis</title>
            <link>http://www.medworm.com/index.php?rid=3313236&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm4j618471u6g3532%2F</link>
            <description>We describe the case of a 59-year-old homosexual man with a 1-month
 history of decreased vision acuity in his left eye who was diagnosed with neurosyphilis and received treatment with intravenous
 penicillin G (16 million units in divided daily doses), with great improvement of visual acuity and CSF examination findings.
 The interest of this case is not only represented by the unusually early ocular involvement, but also by the rapid evolution
 of the disease into the secondary stage in a man who had had one at-risk homosexual relationship only 3&amp;nbsp;months before the
 onset symptoms. We also support the view that the presence of ocular involvement in syphilitic patients is suggestive of involvement
 of the CNS and should be considered synonymous with neurosyphilis.
 
 
	Content Type Jo...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3313236</comments>
            <pubDate>Thu, 25 Feb 2010 06:54:35 +0100</pubDate>
            <guid isPermaLink="false">3313236</guid>        </item>
        <item>
            <title>Exertional reversible cerebral vasoconstriction responsive to verapamil</title>
            <link>http://www.medworm.com/index.php?rid=3313238&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl5857w3741277067%2F</link>
            <description>We present a case of a 25-year-old male with severe headaches associated with exertion and sexual intercourse with vasoconstriction
 on magnetic resonance and CT angiograms done during his typical headaches. The headache syndrome and angiographic findings
 resolved after starting low-dose verapamil. Perhaps, some cases of primary exertional and primary headaches associated with
 sexual activity are associated with reversible cerebral vasoconstriction responsive to calcium channel blockers.
 
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-010-0226-4Authors
		Brett J. Theeler, William Beaumont Army Medical Center, Medical Corps, United States Army Department of Medicine/Neurology Service 5005 N. Piedras, Fort Bliss El Paso TX 79920 USAMichael V. Krasnokutsky, Madigan A...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3313238</comments>
            <pubDate>Thu, 25 Feb 2010 06:54:33 +0100</pubDate>
            <guid isPermaLink="false">3313238</guid>        </item>
        <item>
            <title>S.F. Cappa, J. Abutalebi, J.-F. Demonet, P.C. Fletcher, P. Garrard (eds): Cognitive neurology—a clinical textbook</title>
            <link>http://www.medworm.com/index.php?rid=3313237&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv1w720q8756wjq00%2F</link>
            <description>Content Type Journal ArticleCategory Book ReviewDOI 10.1007/s10072-010-0230-8Authors
		Anna Rita Giovagnoli, Fondazione Istituto Neurologico Carlo Besta Milan Italy
	

	
		Journal Neurological SciencesOnline ISSN 1590-3478Print ISSN 1590-1874 (Source: Neurological Sciences)</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3313237</comments>
            <pubDate>Thu, 25 Feb 2010 06:54:33 +0100</pubDate>
            <guid isPermaLink="false">3313237</guid>        </item>
        <item>
            <title>Myocardial MIBG scintigraphy: a useful clinical tool?</title>
            <link>http://www.medworm.com/index.php?rid=3274222&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn5523684081507r0%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Meta-iodbenzylguanidine scintigraphy (MIBG scintigraphy) shows reduced uptake in idiopathic Parkinson’s disease (IPD), idiopathic
 REM sleep behavior disorder (IRBD) and Lewy body dementia (LBD), but not in other parkinsonian or dementia syndromes. We retrospectively
 reevaluated 50 patients. Concordance rate between last clinical diagnosis and scintigraphy diagnosis was only given in two-thirds
 of the patients. Confounding factors were: decreasing heart/mediastinum ratio (HMR) with progressive age, higher HMR in women
 and possibly interference with antihypertensive medication. Standardization of the methods and precise clinical guidelines
 are warranted for better clinical use.
 
	Content Type Journal ArticleCategory Brief CommunicationDOI 10.1007/s10072-010-0218-4...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3274222</comments>
            <pubDate>Sat, 13 Feb 2010 06:48:08 +0100</pubDate>
            <guid isPermaLink="false">3274222</guid>        </item>
        <item>
            <title>A case of asymptomatic pontine myelinolysis</title>
            <link>http://www.medworm.com/index.php?rid=3270507&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg0036l44626276wu%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Central pontine myelinolysis is an acquired, non-inflammatory demyelinating lesion usually localized in the brainstem pons
 basis; it usually affects patients with a history of chronic alcoholism, malnutrition or dysionemia. The exact pathogenesis
 of myelinolysis is still unclear. A 69-year-old Caucasian male presented intensive headache and underwent cranial MRI that
 showed the typical feature of central pontine myelinolysis. Neurological valuation was negative. Other examinations included
 extensive blood tests, electroencephalogram and multimodal evoked potentials which all gave normal results. Alcohol abuse
 and malabsorption syndrome were excluded. The medical history revealed a continuative use of anti-depressive drugs and exposure
 to glue for years. Our patien...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3270507</comments>
            <pubDate>Thu, 11 Feb 2010 11:48:55 +0100</pubDate>
            <guid isPermaLink="false">3270507</guid>        </item>
        <item>
            <title>Diagnosis, treatment and follow-up of the carpal tunnel syndrome: a review</title>
            <link>http://www.medworm.com/index.php?rid=3264698&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9wk2458050626516%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The carpal tunnel syndrome is a compressive neuropathy with high incidence rates, and its correct diagnosis, treatment and
 follow-up may lead to significant benefits in healthcare, social and economic terms. In this review, based on systematic review
 databases and guidelines, we summarise the appropriate indications for the diagnosis, treatment and follow-up, accompanied,
 whenever possible, by the levels of evidence and strength of recommendations.
 
	Content Type Journal ArticleCategory Review ArticleDOI 10.1007/s10072-009-0213-9Authors
		Calogero Alfonso, Azienda Ospedaliera di Bologna Policlinico S. Orsola-Malpighi U.O. Ortopedia e Traumatologia Via Albertoni, 15 40141 Bologna ItalyStefano Jann, A.O. Ospedale Maggiore Niguarda U.O. Neurologia Piazza Ospedale Maggi...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3264698</comments>
            <pubDate>Tue, 09 Feb 2010 17:45:13 +0100</pubDate>
            <guid isPermaLink="false">3264698</guid>        </item>
        <item>
            <title>Psychogenic axial myoclonus: report on two cases</title>
            <link>http://www.medworm.com/index.php?rid=3247990&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9886260884660w68%2F</link>
            <description>We report on two patients displaying flexion AM
 jerks in the absence of structural lesion of the central nervous system or electrophysiological evidence of organic origin.
 A conversion disorder was diagnosed. The jerks disappeared after psychoeducation with the patients remaining symptom free
 in 6-year long follow-up. The diagnoses of psychogenic axial (propriospinal-like) myoclonus were established. The literature
 on psychogenic axial (propriospinal-like myoclonus) is limited to a case report. Our cases demonstrate a good response to
 psychotropic medication and psychoeducation and fulfill the psychogenic movement disorder criteria. The phenomenology of psychogenic
 abnormal movements is diverse and PSM-like clinical picture may be a novel presentation.
 
	Content Type Journal Article...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3247990</comments>
            <pubDate>Thu, 04 Feb 2010 18:11:45 +0100</pubDate>
            <guid isPermaLink="false">3247990</guid>        </item>
        <item>
            <title>Intraoperative microrecordings in the posterior hypothalamus of anaesthetized humans with aggressive behaviour</title>
            <link>http://www.medworm.com/index.php?rid=3247991&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg7j3068639576108%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Two patients with uncontrollable aggressive behaviour underwent the placement of stimulating leads in the posterior hypothalamus
 (pHyp). One patient had also multifocal refractory epilepsy. Microrecordings were obtained in both patients during surgery
 under general anaesthesia. Firing rate, interspike intervals and oscillatory discharge patterns were analysed in 14 neurons.
 A mean discharge rate of 19&amp;nbsp;Hz, and oscillatory activity at 7–8&amp;nbsp;Hz were recorded in the first patient with aggressiveness
 and epilepsy. In the second patient the mean firing rate was 10&amp;nbsp;Hz, with evidence of both tonic and random firing patterns.
 Previous studies in patients with cluster headache showed that a discharge rate around 20&amp;nbsp;Hz and lack of a specific rhythmic
 patt...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3247991</comments>
            <pubDate>Thu, 04 Feb 2010 18:11:44 +0100</pubDate>
            <guid isPermaLink="false">3247991</guid>        </item>
        <item>
            <title>Protective effects of heme oxygenase-1 against MPP+-induced cytotoxicity in PC-12 cells</title>
            <link>http://www.medworm.com/index.php?rid=3241614&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft7k3h54720263817%2F</link>
            <description>This study examined whether HO-1 can be
 induced by MPP+ and whether HO-1 has a protective role against the MPP+-induced cytotoxicity in PC-12 cells. MPP+ triggered a relatively rapid induction of HO-1. The MPP+-induced cytotoxicity and reactive oxygen species (ROS) production markedly increased by HO-1 inhibitor, zinc protoporphyrin-IX
 (ZnPP-IX). The increase of ROS production by ZnPP-IX was completely abrogated by either two products of HO (biliverdin or
 bilirubin) while the increase of cytotoxicity by ZnPP-IX was attenuated partially. These suggest that HO-1 expression might
 have some cytoprotective effect against MPP+-induced cytotoxicity.
 
	Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s10072-010-0216-6Authors
		Jung-Woo Bae, Sungkyunkwan University Laboratory o...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3241614</comments>
            <pubDate>Wed, 03 Feb 2010 06:49:23 +0100</pubDate>
            <guid isPermaLink="false">3241614</guid>        </item>
        <item>
            <title>Deep-brain stimulation of the nucleus accumbens in obsessive compulsive disorder: clinical, surgical and electrophysiological considerations in two consecutive patients</title>
            <link>http://www.medworm.com/index.php?rid=3241615&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj591224h8210l650%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Obsessive compulsive disorder is a highly disabling pathological condition which in the most severe and drug-resistant form
 can severely impair social, cognitive and interpersonal functioning. Deep-brain stimulation has been demonstrated to be an
 effective and safe interventional procedure in such refractory forms in selected cases. We here report the first Italian experience
 in the treatment of this pathology by means of nucleus accumbens stimulation, pointing out to some technical data which could
 be of help in localization of the target.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0214-8Authors
		Angelo Franzini, Fondazione Istituto Nazionale Neurologico “Carlo Besta” Via Caloria 11 20133 Milan ItalyGiuseppe Messina, Fondazione I...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3241615</comments>
            <pubDate>Wed, 03 Feb 2010 06:49:20 +0100</pubDate>
            <guid isPermaLink="false">3241615</guid>        </item>
        <item>
            <title>Air pollution positively correlates with daily stroke admission and in hospital mortality: a study in the urban area of Como, Italy</title>
            <link>http://www.medworm.com/index.php?rid=3229309&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk070n26244723842%2F</link>
            <description>In conclusion, this study suggests an association between short-term outdoor air pollution
 exposure and ischemic stroke admission and mortality.
 
	Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s10072-009-0206-8Authors
		Simone Vidale, Sant’Anna Hospital Neurology Department Via Napoleona 60 22100 Como ItalyA. Bonanomi, Cattolica Sacro Cuore University Statistic Sciences Department Milan ItalyM. Guidotti, Valduce Hospital Neurology Department Como ItalyM. Arnaboldi, Sant’Anna Hospital Neurology Department Via Napoleona 60 22100 Como ItalyR. Sterzi, Niguarda Ca’ Granda Hospital Neurology Department Milan Italy
	

	
		Journal Neurological SciencesOnline ISSN 1590-3478Print ISSN 1590-1874 (Source: Neurological Sciences)</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3229309</comments>
            <pubDate>Sat, 30 Jan 2010 18:13:01 +0100</pubDate>
            <guid isPermaLink="false">3229309</guid>        </item>
        <item>
            <title>SIADH following pituitary adenoma apoplexy</title>
            <link>http://www.medworm.com/index.php?rid=3229308&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu231672776104787%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The rare case of a patient with SIADH following pituitary adenoma apoplexy is reported. Since apoplexy did not exert any mass
 effect on surrounding structures, the patient was treated conservatively and the anterior pituitary gland insufficiency has
 been substituted adequately. Seven days after the apoplexy the patient again showed low serum–Na+ levels despite cortisol substitution. Diagnosis of SIADH was made. It is essential to be aware of this rare syndrome in patients
 with pituitary adenoma apoplexy.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0210-zAuthors
		Florian Heinrich Ebner, Eberhard-Karls-University Hospital Tübingen Department of Neurosurgery Hoppe-Seyler-Straße 3 72076 Tübingen GermanyTill K. Hauser, Eberhard-Karls-Un...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3229308</comments>
            <pubDate>Sat, 30 Jan 2010 18:13:01 +0100</pubDate>
            <guid isPermaLink="false">3229308</guid>        </item>
        <item>
            <title>Posterior reversible encephalopathy and alexia without agraphia in a patient with Hashimoto’s encephalopathy</title>
            <link>http://www.medworm.com/index.php?rid=3229311&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj263ur2j24331814%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorDOI 10.1007/s10072-009-0212-xAuthors
		Ozlem Kayim Yildiz, Cumhuriyet University School of Medicine Department of Neurology 58140 Sivas TurkeyHatice Segmen, Cumhuriyet University School of Medicine Department of Neurology 58140 Sivas TurkeyIbrahim Oztoprak, Cumhuriyet University School of Medicine Department of Radiology 58140 Sivas TurkeyErtugrul Bolayir, Cumhuriyet University School of Medicine Department of Neurology 58140 Sivas TurkeySuat Topaktas, Cumhuriyet University School of Medicine Department of Neurology 58140 Sivas Turkey
	

	
		Journal Neurological SciencesOnline ISSN 1590-3478Print ISSN 1590-1874 (Source: Neurological Sciences)</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3229311</comments>
            <pubDate>Sat, 30 Jan 2010 18:13:00 +0100</pubDate>
            <guid isPermaLink="false">3229311</guid>        </item>
        <item>
            <title>Herpetic inflammation of multiple cranial nerves</title>
            <link>http://www.medworm.com/index.php?rid=3229310&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ftlk4404005771157%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorDOI 10.1007/s10072-009-0208-6Authors
		Kamyar Ghabili, Tabriz University of Medical Sciences Tuberculosis and Lung Diseases Research Center Golgasht St. Tabriz IranMohammadali M. Shoja, Indianapolis Neurosurgical Group, Clarian Neuroscience Institute Indianapolis IN USAR. Shane Tubbs, Children’s Hospital Section of Pediatric Neurosurgery Birmingham AL USAAaron A. Cohen-Gadol, Indianapolis Neurosurgical Group, Clarian Neuroscience Institute Indianapolis IN USA
	

	
		Journal Neurological SciencesOnline ISSN 1590-3478Print ISSN 1590-1874 (Source: Neurological Sciences)</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3229310</comments>
            <pubDate>Sat, 30 Jan 2010 18:13:00 +0100</pubDate>
            <guid isPermaLink="false">3229310</guid>        </item>
        <item>
            <title>Reversibility of brain lesions in a case of Neuro-Behçet’s disease studied by MR diffusion</title>
            <link>http://www.medworm.com/index.php?rid=3229312&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F248371l7424k34j8%2F</link>
            <description>We describe the case of a patient with NBD studied with conventional and diffusion weighted MR imaging.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0205-9Authors
		Luisa Vuolo, University of Genoa DINOG, Department of Neurosciences, Ophthalmology and Genetics Via De Toni, 5 16132 Genoa ItalyLaura Bonzano, University of Genoa DINOG, Department of Neurosciences, Ophthalmology and Genetics Via De Toni, 5 16132 Genoa ItalyCaterina Roccatagliata, Azienda Sanitaria Locale 3 Genoa ItalyRoberto Carlo Parodi, San Martino Hospital Neuroradiology Unit Genoa ItalyLuca Roccatagliata, University of Genoa DINOG, Department of Neurosciences, Ophthalmology and Genetics Via De Toni, 5 16132 Genoa Italy
	

	
		Journal Neurological SciencesOnline ISSN 1590-3478Print ISSN 1590-187...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3229312</comments>
            <pubDate>Sat, 30 Jan 2010 18:12:58 +0100</pubDate>
            <guid isPermaLink="false">3229312</guid>        </item>
        <item>
            <title>Insulinoma presenting as idiopathic hypersomnia</title>
            <link>http://www.medworm.com/index.php?rid=3229313&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh833p86p62r67671%2F</link>
            <description>We report the case of a 32-year-old woman with a history of increased sleep need and difficulty waking up; the diagnosis of
 idiopathic hypersomnia was hypothesized. During ambulatory polysomnography (PSG), the patient presented an episode characterized
 by loss of consciousness and jerking of the four limbs. A video-PSG monitoring was performed and the patient showed unresponsiveness
 and drowsiness at 7&amp;nbsp;a.m. During the episode, EEG showed theta–delta diffuse activity, and blood glucose level was 32&amp;nbsp;mg&amp;nbsp;dl−1. The diagnosis of insulinoma was then assumed; CT scan showed a hypodense mass into the pancreatic tail, and a partial pancreasectomy
 was performed. The described symptoms disappeared, and 5&amp;nbsp;years later the findings of a complete clinical and neurophysiological...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3229313</comments>
            <pubDate>Sat, 30 Jan 2010 18:12:55 +0100</pubDate>
            <guid isPermaLink="false">3229313</guid>        </item>
        <item>
            <title>Serum levels of brain-derived neurotrophic factor in Sydenham’s chorea</title>
            <link>http://www.medworm.com/index.php?rid=3229314&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr14151mmv5355211%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Sydenham’s chorea (SC) is the neurologic manifestation of rheumatic fever. In addition to involuntary movements, SC patients
 show behavioral changes, such as hyperactivity, obsessions, and compulsions. Brain-derived neurotrophic factor (BDNF) is related
 to neuronal development and differentiation. Since BDNF serum levels are altered in a series of neuropsychiatric disorders,
 such as schizophrenia and Huntington’s disease, we investigated the serum levels of BDNF in SC patients. Eighteen patients
 with acute SC, 4 with persistent SC and 27 control subjects were included in this study. BDNF was determined by ELISA. There
 was no significant difference between BDNF serum levels of control and acute SC groups (P&amp;nbsp;=&amp;nbsp;0.12). Persistent SC patients presented dec...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3229314</comments>
            <pubDate>Fri, 29 Jan 2010 12:16:43 +0100</pubDate>
            <guid isPermaLink="false">3229314</guid>        </item>
        <item>
            <title>Upper airways obstruction due to retrosternal goiter in a patient with myasthenia gravis</title>
            <link>http://www.medworm.com/index.php?rid=3229315&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg132l7253047q056%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorDOI 10.1007/s10072-009-0203-yAuthors
		Fabio Poglio, AOU San Giovanni Battista Neurologia IV, Dipartimento di Neuroscienze Via Cherasco 15 10126 Turin ItalyIlaria Paolasso, AOU San Giovanni Battista Neurologia IV, Dipartimento di Neuroscienze Via Cherasco 15 10126 Turin ItalyYolanda Falcone, AOU San Giovanni Battista Neurologia IV, Dipartimento di Neuroscienze Via Cherasco 15 10126 Turin ItalySerena Grimaldi, AOU San Giovanni Battista Neurologia IV, Dipartimento di Neuroscienze Via Cherasco 15 10126 Turin ItalyDario Cocito, AOU San Giovanni Battista Neurologia IV, Dipartimento di Neuroscienze Via Cherasco 15 10126 Turin Italy
	

	
		Journal Neurological SciencesOnline ISSN 1590-3478Print ISSN 1590-1874 (Source: Neurological Science...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3229315</comments>
            <pubDate>Fri, 29 Jan 2010 12:16:40 +0100</pubDate>
            <guid isPermaLink="false">3229315</guid>        </item>
        <item>
            <title>Vertebroplasty for pain relief and spinal stabilization in multiple myeloma</title>
            <link>http://www.medworm.com/index.php?rid=3191248&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fjn775104706k1p4u%2F</link>
            <description>In conclusion, vertebroplasty is a safe and efficient procedure in the treatment of painful vertebral body fractures in patients
 with multiple myeloma, without potential contraindications, such as fractures of the posterior wall or epidural disease. We
 also treated three and more levels in 28% of cases in a single session without complications. Due to the early pain relief
 and the low complication rate, it is possible to expand the indication to vertebroplasty for the prophylactic augmentation
 of those vertebral bodies at risk of fracture in which significant neoplastic substitution of the body is present.
 
	Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s10072-009-0197-5Authors
		Flavio Tancioni, Instituto Clinico Humanitas Department of Neurosurgery Milan ItalyMart...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3191248</comments>
            <pubDate>Fri, 15 Jan 2010 00:42:57 +0100</pubDate>
            <guid isPermaLink="false">3191248</guid>        </item>
        <item>
            <title>Childhood-onset HAM/TSP with progressive cognitive impairment</title>
            <link>http://www.medworm.com/index.php?rid=3191249&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2172472558nh5466%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;HTLV-I associated myelopathy/tropical spastic paraparesis (HAM/TSP) is a chronic myelopathy, usually with adult-onset. Very
 few cases of childhood-onset have been described, most presenting with progressive paraparesis and sphincteric disturbances
 as in the adult form. Here we report a young male with childhood-onset of HAM/TSP and progressive cognitive and behavioral
 disturbances. A serological screening revealed HTLV-I infection, confirmed by Western Immunoblotting analysis. Molecular characterization
 of amplified HTLV-I proviral DNA has been performed both in the patient and his mother by LTR sequence analysis, and HLA genotype
 inheritance was evaluated. Our case indicates the possibility that cognitive dysfunctions may be one manifestation of HTLV-I
 infection ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3191249</comments>
            <pubDate>Fri, 15 Jan 2010 00:42:56 +0100</pubDate>
            <guid isPermaLink="false">3191249</guid>        </item>
        <item>
            <title>Bilateral whirlbone necrosis in a young multiple sclerosis patient</title>
            <link>http://www.medworm.com/index.php?rid=3169354&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv42h273663216572%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A case of avascular necrosis of whirlbone in a young man affected by multiple sclerosis and treated with high doses of corticosteroids
 is described. The authors discuss the causes of this collateral effect underlining the risks of underevaluating the symptoms.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0177-9Authors
		Edvina Galiè, Istituto Nazionale Tumori Regina Elena Division of Neurology Via Chianesi 53 00144 Rome ItalyBruno Jandolo, Istituto Nazionale Tumori Regina Elena Division of Neurology Via Chianesi 53 00144 Rome Italy
	

	
		Journal Neurological SciencesOnline ISSN 1590-3478Print ISSN 1590-1874 (Source: Neurological Sciences)</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3169354</comments>
            <pubDate>Tue, 12 Jan 2010 06:44:48 +0100</pubDate>
            <guid isPermaLink="false">3169354</guid>        </item>
        <item>
            <title>Role of matrix metalloproteinase-9 in apoptosis of hippocampal neurons in rats during early brain injury after subarachnoid hemorrhage</title>
            <link>http://www.medworm.com/index.php?rid=3122812&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw200k6n3k243206k%2F</link>
            <description>This study investigated the possible involvement of matrix metalloproteinase 9 (MMP-9) in early brain injury (EBI) of subarachnoid
 hemorrhage (SAH) in rats. MMP-9 activities in hippocampus were examined at 6, 12, 24, 48 and 72&amp;nbsp;h after SAH. Laminin was detected
 by immunohistochemistry. Apoptosis of neurons in hippocampus was observed by TUNEL. Brain water content was also examined.
 MMP-9 activity and the number of apoptotic neurons increased from 12 to 72&amp;nbsp;h with a peak at 24&amp;nbsp;h. Laminin was found to decrease
 at 12&amp;nbsp;h, reached minimum at 24&amp;nbsp;h and began to increase from 48&amp;nbsp;h, which had a negative correlation with apoptotic neurons.
 The changes of brain water content were found to be coincidence with that of neuronal apoptosis. Our findings suggest that
 MMP-9 ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3122812</comments>
            <pubDate>Thu, 24 Dec 2009 19:57:49 +0100</pubDate>
            <guid isPermaLink="false">3122812</guid>        </item>
        <item>
            <title>Migraine and cerebral infarction in young people</title>
            <link>http://www.medworm.com/index.php?rid=3122813&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fdgl8822133036384%2F</link>
            <description>In conclusion, migraine with aura appears to be associated with ischemic stroke in young women, independently
 from other common risk factors.
 
	Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s10072-009-0195-7Authors
		Massimo Camerlingo, Policlinico San Marco Neurological Unit Corso Europa 7 24040 Osio Sotto Bergamo ItalyA. Romorini, Presidio Ospedaliero Neurological Unit Magenta Milano ItalyC. Ferrante, Policlinico San Marco Neurological Unit Corso Europa 7 24040 Osio Sotto Bergamo ItalyL. Valente, Policlinico San Marco Neurological Unit Corso Europa 7 24040 Osio Sotto Bergamo ItalyL. Moschini, Policlinico San Marco Neurological Unit Corso Europa 7 24040 Osio Sotto Bergamo Italy
	

	
		Journal Neurological SciencesOnline ISSN 1590-3478Print ISSN 1590-1874 (Source: Neur...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3122813</comments>
            <pubDate>Thu, 24 Dec 2009 19:57:48 +0100</pubDate>
            <guid isPermaLink="false">3122813</guid>        </item>
        <item>
            <title>Natural history of Charcot–Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life</title>
            <link>http://www.medworm.com/index.php?rid=3106062&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh17543uk563k2308%2F</link>
            <description>We report the
 results of the natural history of clinical features and quality of life (QoL) in patients with CMT2. Twenty patients were
 enrolled. At recruitment and at follow-up (2&amp;nbsp;years), all patients underwent neurological evaluation, QoL and disability assessments.
 The study-end evaluation took place 20–28&amp;nbsp;months after the baseline evaluation. During the 2-year follow-up period, CMT2 patients
 showed a mild reduction of strength of distal muscles of upper limbs and proximal muscles of lower limbs, a worsening sensory
 function and a mild increase in walking disability. However, there was no relevant worsening of QoL, except for a mild deterioration
 of one mental health domain.
 
	Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s10072-009-0202-zAuthors
		...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3106062</comments>
            <pubDate>Thu, 17 Dec 2009 07:04:15 +0100</pubDate>
            <guid isPermaLink="false">3106062</guid>        </item>
        <item>
            <title>Reported quality of randomized controlled trials in neglect rehabilitation</title>
            <link>http://www.medworm.com/index.php?rid=3086932&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb44h6q650762u310%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of this study is to assess the reported quality of randomized controlled trials (RCTs) on the effectiveness of neglect
 rehabilitation using a standardized scale. A search of seven electronic databases was carried out. Selected articles were
 scored using the PEDro scale and classified as high or low quality study both with the original cut off of 6 and a modified
 cut off of 5. A linear regression analysis between year of publication and quality rate was used to test whether the quality
 of the studies improved with time. A total of 18 RCTs were selected. Six articles (33.3%) and 10 articles (55.56%) were classified
 as having high quality when the original cut off or the modified cut off of the PEDro scale were used, respectively. Analysis
 shows no time-relat...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3086932</comments>
            <pubDate>Thu, 10 Dec 2009 15:19:15 +0100</pubDate>
            <guid isPermaLink="false">3086932</guid>        </item>
        <item>
            <title>Acute subdural hemorrhage associated with rifampicin-induced thrombocytopenia</title>
            <link>http://www.medworm.com/index.php?rid=3064968&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp4t726055307v703%2F</link>
            <description>We report a patient with acute subdural hemorrhage associated with rifampicin-induced thrombocytopenia.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0187-7Authors
		Sa-Yoon Kang, Cheju National University Department of Neurology, College of Medicine Jeju South KoreaJay Chol Choi, Cheju National University Department of Neurology, College of Medicine Jeju South KoreaJi-Hoon Kang, Cheju National University Department of Neurology, College of Medicine Jeju South KoreaJung Seok Lee, Cheju National University Department of Neurology, College of Medicine Jeju South Korea
	

	
		Journal Neurological SciencesOnline ISSN 1590-3478Print ISSN 1590-1874 (Source: Neurological Sciences)</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3064968</comments>
            <pubDate>Fri, 04 Dec 2009 07:19:49 +0100</pubDate>
            <guid isPermaLink="false">3064968</guid>        </item>
        <item>
            <title>Association between interleukin-6 gene promoter −572C/G polymorphism and the risk of sporadic Alzheimer’s disease</title>
            <link>http://www.medworm.com/index.php?rid=3064969&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr4184618401x603q%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Inflammation is a key component of Alzheimer’s disease (AD), and we have examined the effect of two polymorphisms (−174G/C
 and −572C/G) in the promoter of the inflammatory cytokine interleukin-6 (IL-6) gene on risk of AD in 318 AD patients. Significant
 differences in genotype and allele frequencies of −572C/G IL-6 promoter polymorphism were observed between AD patients and
 controls. The GG genotype was associated with a decreased risk of developing AD (OR 0.423, 95% CI 0.200–0.894). Similarly,
 logistic regression analysis revealed that G allele was a protective factor for AD (OR 0.732, 95% CI 0.567–0.945). For −174G/C
 variability, no C variability was found in all the subjects. The frequency of the IL-6 −174G/C promoter polymorphism is very
 low or ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3064969</comments>
            <pubDate>Thu, 03 Dec 2009 12:50:05 +0100</pubDate>
            <guid isPermaLink="false">3064969</guid>        </item>
        <item>
            <title>Candidate gene analysis of semaphorins in patients with Alzheimer’s disease</title>
            <link>http://www.medworm.com/index.php?rid=3064970&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh463883410h7126n%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Semaphorins of the SemaIV family are expressed in neurons and decreased in brains from patients with Alzheimer’s disease (AD).
 Accumulation of an internalized form of Sema3A is associated with degeneration of neurons, making these molecules candidates
 for the development of AD. Single nucleotide polymorphisms (SNPs) rs36026860 and rs28469467 in Sema3A as well as rs13284404 and rs11526468 in Sema4D were analyzed in a population of 240 patients with AD compared with 222 age-matched controls. None of SNPs in Sema3A were present, either in patients or controls. The distribution of the Sema4D rs11526468 and rs13284404 SNPs was not significantly different between patients and controls, even stratifying for gender
 or age at onset. In silico analysis predicted that rs11526...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3064970</comments>
            <pubDate>Thu, 03 Dec 2009 12:50:04 +0100</pubDate>
            <guid isPermaLink="false">3064970</guid>        </item>
        <item>
            <title>Sudden death in Unverricht–Lundborg patients: is serotonin the key?</title>
            <link>http://www.medworm.com/index.php?rid=3064971&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk582v716978g0k60%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorDOI 10.1007/s10072-009-0193-9Authors
		Pasquale Striano, University of Genova Muscular and Neurodegenerative Diseases Unit, G. Gaslini Institute Genova ItalyElena D’Amato, University of Genova Department of Paediatrics, G. Gaslini Institute Genova ItalyMarianna Pezzella, Federico II University Epilepsy Center Naples ItalyPaolo Mainardi, University of Genova Department of Neurosciences, Ophthalmology and Genetics, Ospedale S. Martino Genova ItalyFederico Zara, University of Genova Muscular and Neurodegenerative Diseases Unit, G. Gaslini Institute Genova ItalySalvatore Striano, Federico II University Epilepsy Center Naples Italy
	

	
		Journal Neurological SciencesOnline ISSN 1590-3478Print ISSN 1590-1874 (Source: Neurological Scie...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3064971</comments>
            <pubDate>Tue, 01 Dec 2009 21:01:20 +0100</pubDate>
            <guid isPermaLink="false">3064971</guid>        </item>
        <item>
            <title>BRD2 and TAP-1 genes and juvenile myoclonic epilepsy</title>
            <link>http://www.medworm.com/index.php?rid=3064972&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft9617l724l76x890%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Juvenile myoclonic epilepsy (JME) is a genetically determined common subtype of idiopathic generalized epilepsy. Linkage of
 JME to the chromosomal region 6p21.3 has been reported. An association has been previously observed between JME and the positional
 candidate, 6p21.3 linked, BRD2. Another candidate in this region is the TAP-1 gene encoding the Transporter Associated with Antigen Processing. The aim
 of the present study is to determine whether these two genes modulate the vulnerability to JME. While no difference was observed
 in the allele and genotype frequencies of BRD2 between JME and controls, an association was found between a TAP-1 haplotype and JME, suggesting that this gene may be another 6p21.3 linked vulnerability factor to JME.
 
	Content Type Journal...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3064972</comments>
            <pubDate>Tue, 01 Dec 2009 21:01:18 +0100</pubDate>
            <guid isPermaLink="false">3064972</guid>        </item>
        <item>
            <title>Absence of aprataxin gene mutations in a Greek cohort with sporadic early onset ataxia and normal GAA triplets in frataxin gene</title>
            <link>http://www.medworm.com/index.php?rid=3064973&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj8m5648224017580%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Phenotype of patients with the aprataxin gene mutation varies and according to previous studies, screening of aprataxin gene
 could be useful, once frataxin gene mutation is excluded in patients with normal GAA expansion in frataxin gene. In the present
 study, we sought to determine possible causative mutations in aprataxin gene (all exons and flanking intronic sequences) in
 14 Greek patients with sporadic cerebellar ataxia all but one without GAA expansion in frataxin gene (1 patient was heterozygous).
 No detectable point mutation or deletion was found in the aprataxin gene of all the patients. Our results do not confirm the
 previous studies. This difference may be attributed to the different populations studied and possible different genetic background.
 It is sti...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3064973</comments>
            <pubDate>Tue, 01 Dec 2009 21:01:16 +0100</pubDate>
            <guid isPermaLink="false">3064973</guid>        </item>
        <item>
            <title>Good maternal and fetal outcomes of predominantly sensory Guillain–Barré syndrome in pregnancy after intravenous immunoglobulin</title>
            <link>http://www.medworm.com/index.php?rid=3041804&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu3523r3723777469%2F</link>
            <description>We reported a case of good maternal and fetal outcomes of predominantly sensory GBS (generalized pain and numbness,
 mild deep sensory ataxia, positive serum IgM anti-GalNAcGD1a antibody)-complicating pregnancy after intravenous immunoglobulin
 treatment.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0188-6Authors
		Yasuo Matsuzawa, Toho University Respiratory Diseases Division, Department of Internal Medicine, Sakura Medical Center Sakura JapanRyuji Sakakibara, Toho University Neurology Division, Department of Internal Medicine, Sakura Medical Center 564-1 Shimoshizu Sakura 285-8741 JapanToshiko Shoda, Toho University Respiratory Diseases Division, Department of Internal Medicine, Sakura Medical Center Sakura JapanMasahiko Kishi, Toho University Neurology Divis...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3041804</comments>
            <pubDate>Wed, 25 Nov 2009 16:50:49 +0100</pubDate>
            <guid isPermaLink="false">3041804</guid>        </item>
        <item>
            <title>Erratum to: Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients</title>
            <link>http://www.medworm.com/index.php?rid=3032236&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1qw14l010k084458%2F</link>
            <description>Content Type Journal ArticleCategory ErratumDOI 10.1007/s10072-009-0196-6Authors
		Alessandro Consales, Gaslini Children’s Hospital Department of Neurosurgery Genoa ItalyGianluca Piatelli, Gaslini Children’s Hospital Department of Neurosurgery Genoa ItalyMarcello Ravegnani, Gaslini Children’s Hospital Department of Neurosurgery Genoa ItalyMarco Pavanello, Gaslini Children’s Hospital Department of Neurosurgery Genoa ItalyPasquale Striano, Gaslini Children’s Hospital Department of Muscular and Neurodegenerative Diseases Genoa ItalyMaria Luisa Zoli, National Health Service Department of Assistance for the Disabled Genoa ItalyValeria Capra, Gaslini Children’s Hospital Department of Neurosurgery Genoa ItalyAndrea Rossi, Gaslini Children’s Hospital Department of Neuroradiology Ge...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3032236</comments>
            <pubDate>Tue, 24 Nov 2009 07:10:27 +0100</pubDate>
            <guid isPermaLink="false">3032236</guid>        </item>
        <item>
            <title>Amyotrophic lateral sclerosis mimic syndrome due to a dorsal spinal cord neurofibroma</title>
            <link>http://www.medworm.com/index.php?rid=3032237&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg827q567g2038346%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorDOI 10.1007/s10072-009-0186-8Authors
		Andrea Calvo, University of Torino Section of Neurology, Department of Neuroscience Via Cherasco 15 10126 Turin ItalyFranco Benech, University of Torino Section of Neurosurgery, Department of Neuroscience Turin ItalyPaolo Ghiglione, Ospedale Maggiore Savigliano ItalyMichele Balma, University of Torino Section of Neurology, Department of Neuroscience Via Cherasco 15 10126 Turin ItalyCristina Moglia, University of Torino Section of Neurology, Department of Neuroscience Via Cherasco 15 10126 Turin ItalyRoberto Mutani, University of Torino Section of Neurology, Department of Neuroscience Via Cherasco 15 10126 Turin ItalyAdriano Chiò, University of Torino Section of Neurology, Department of Neuros...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3032237</comments>
            <pubDate>Tue, 24 Nov 2009 07:10:26 +0100</pubDate>
            <guid isPermaLink="false">3032237</guid>        </item>
        <item>
            <title>Genetic bases of comorbidity between mood disorders and migraine: possible role of serotonin transporter gene</title>
            <link>http://www.medworm.com/index.php?rid=3020840&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0x7x6262t1767u33%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Migraine is a common neurological disease in the population and the most associated headache with mood disorder. Although
 the relationship between migraine and depression is well known, the reverse correlation between depression and migraine was
 observed but not well understood. The tight relationship between the two disturbances is also suggested by the efficacy of
 antidepressants for migraine treatment. Starting from these observations, we can presume that both migraine and depression
 have overlapping biological bases. The main target of antidepressant treatments belonging to the serotonin selective reuptake
 inhibitors (SSRI) type is the serotonin transporter (SERT); a well-studied polymorphic variant, in the promoter region of
 the gene (SERTPR), has been demons...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3020840</comments>
            <pubDate>Sat, 21 Nov 2009 08:30:51 +0100</pubDate>
            <guid isPermaLink="false">3020840</guid>        </item>
        <item>
            <title>Micturitional disturbance due to bilateral medial frontal lobe lesions in a patient with multiple sclerosis</title>
            <link>http://www.medworm.com/index.php?rid=3020839&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F888213g0w6066m15%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 41-year-old man with multiple sclerosis (MS) complained of nocturnal enuresis at the third exacerbation. Neurological examination
 revealed echopraxia, forced grasp reflexes and palmo-mental reflexes. The urodynamic studies showed neither spinal cord nor
 peripheral nerve involvements. His brain magnetic resonance images (MRIs) revealed new lesions at the bilateral medial frontal
 lobes. The intravenous methylprednisolone therapy improved nocturnal enuresis and made brain MRI lesions smaller and gone.
 In addition to frequently observed spinal cord lesions, we should consider some medial frontal lesions to be responsible for
 micturitional disturbance in patients with MS.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0189-5Authors
		Sachiko...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3020839</comments>
            <pubDate>Sat, 21 Nov 2009 08:30:51 +0100</pubDate>
            <guid isPermaLink="false">3020839</guid>        </item>
        <item>
            <title>Social support and self-efficacy in patients with Myasthenia Gravis: a common pathway towards positive health outcomes</title>
            <link>http://www.medworm.com/index.php?rid=3020841&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp35332hu7n154145%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Social support and self-efficacy, that was defined as one’s belief in one’s capabilities to enact a certain behaviour, have
 a mediating effect on health outcomes and, by facilitating healthy behaviours and compliance to treatment, reduce morbidity
 and mortality. This pilot study aims to test whether social support and self-efficacy have a positive effect in improving
 health outcomes of patients with Myasthenia Gravis. 74 patients (mean age 48.1; 67.6% female) were enrolled and reported low
 self-efficacy and health status, but good perceived social support. Men reported better self-efficacy than women, and those
 living with a partner reported higher social support levels. No differences were found stratifying for disease onset, disease
 stage and patients’ wor...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3020841</comments>
            <pubDate>Sat, 21 Nov 2009 08:30:50 +0100</pubDate>
            <guid isPermaLink="false">3020841</guid>        </item>
        <item>
            <title>Paradoxical brain embolism caused by an arterial−venous fistula: a diagnostic pitfall</title>
            <link>http://www.medworm.com/index.php?rid=3020842&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx2240x7310886846%2F</link>
            <description>We report on a case of paradoxical embolism across
 a subclavian arterial–venous fistula. This case underlines the necessity of performing the ceTCD, as in this condition the
 right to left shunt could be detected by means of ceTCD, whereas the TEE reveals regular findings.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0185-9Authors
		Piergiorgio Lochner, University Hospital Giessen Department of Neurology Am Steg 14 35392 Giessen GermanyFrediano Tezzon, Franz Tappeiner Hospital Department of Neurology Meran ItalyRafaelle Nardone, Franz Tappeiner Hospital Department of Neurology Meran ItalyChristian Tanislav, University Hospital Giessen Department of Neurology Am Steg 14 35392 Giessen Germany
	

	
		Journal Neurological SciencesOnline ISSN 1590-3478Print ISSN ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3020842</comments>
            <pubDate>Sat, 21 Nov 2009 08:30:49 +0100</pubDate>
            <guid isPermaLink="false">3020842</guid>        </item>
        <item>
            <title>CSF proteomic analysis in patients with normal pressure hydrocephalus selected for the shunt: CSF biomarkers of response to surgical treatment</title>
            <link>http://www.medworm.com/index.php?rid=3020843&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe12275g51328m624%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of our pilot study was to investigate, by a proteomic approach, the expressed differences in cerebrospinal fluid (CSF)
 protein patterns in order to aid in the diagnosis and treatment of normal pressure hydrocephalus (NPH). Seventeen patients
 with NPH, selected by Intracranial-Pressure monitoring (ICPmo), underwent implantation of a shunt and after 6 months were
 clinically re-evaluated. Thirteen patients improved, whereas four did not. During ICPmo CSF was collected and its proteoma
 was analyzed by 2D gel electrophoresis and mass spectrometry. The over-expression of α2HS glycoprotein, α1 antichimotrypsin
 and α1beta glycoprotein and the under-expression of glial fibrillary acidic protein, apolipoproteins (AIV, J and E), complement
 C3c, anti-thrombin, α2 ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3020843</comments>
            <pubDate>Sat, 21 Nov 2009 08:30:48 +0100</pubDate>
            <guid isPermaLink="false">3020843</guid>        </item>
        <item>
            <title>Psoriasis during interferon beta treatment for multiple sclerosis</title>
            <link>http://www.medworm.com/index.php?rid=3016358&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fxxg8117621676kl7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Previous reports have suggested an increased risk of psoriasis in MS patients. Worsening of dermatologic lesions during interferon
 therapy has been rarely reported, but activation of psoriatic arthritis has not been described until now. The following is
 a case report. A 37-year-old woman affected by relapsing–remitting multiple sclerosis had severe worsening of cutaneous psoriasis
 and activation of psoriatic arthritis during interferon beta treatment. The symptoms resolved after therapy discontinuation.
 This case further supports that activation of psoriasis might be a rare side effect of IFNB therapy and suggests careful evaluation
 of concomitant morbidity to allow a patient-oriented treatment strategy.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3016358</comments>
            <pubDate>Thu, 19 Nov 2009 07:47:32 +0100</pubDate>
            <guid isPermaLink="false">3016358</guid>        </item>
        <item>
            <title>GAB2 is not associated with late-onset Alzheimer’s disease in Chinese Han</title>
            <link>http://www.medworm.com/index.php?rid=3016359&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn514h6846w262h13%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;It has recently been shown that GAB2 alleles modify the risk for late-onset Alzheimer disease (LOAD) in apolipoprotein E (ApoE)ε4
 allele carriers in a genome-wide association study. Some studies subsequently in Caucasians population, though not all, have
 demonstrated that GAB2 polymorphisms might be associated with LOAD susceptibility. The aim of this study is to evaluate the
 reported polymorphisms (rs2373115 and rs1385600) and GAB2 haplotypes (rs2373115–rs1385600) for an interaction with the ApoEε4
 allele in a cohort of Chinese LOAD. We conducted a case–control study in 292 LOAD and 227 non-demented controls from the Chinese
 Han population. Our study does not find any association between the two tested SNPs and GAB2 haplotypes and LOAD or any synergetic
 int...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3016359</comments>
            <pubDate>Thu, 19 Nov 2009 07:47:15 +0100</pubDate>
            <guid isPermaLink="false">3016359</guid>        </item>
        <item>
            <title>Prevalence of stroke and stroke-related disability in Valle d’Aosta, Italy</title>
            <link>http://www.medworm.com/index.php?rid=3016360&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6743301677w05h25%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Population ageing and improved healthcare may lead to an increase in the prevalence of stroke. The aim of this study is to
 investigate the prevalence of stroke and stroke-related disability in a population sample resident in Aosta, Italy. The information
 was collect using a simple questionnaire for first ever stroke in the past combined with the analysis of the patients’ medical
 records and integrated with the information reported by six general practitioners. 102 cases of stroke were identified in
 the study population of 6,930 subjects, for an overall prevalence per 1,000 inhabitants of 1.4 (95% CI 0.81–1.99), which increased
 to 4.79 (95% CI 3.29–6.29) in subjects aged ≥65&amp;nbsp;years. Fifty-nine percent of the cases were completely or partially dependent
 ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3016360</comments>
            <pubDate>Thu, 19 Nov 2009 07:47:13 +0100</pubDate>
            <guid isPermaLink="false">3016360</guid>        </item>
        <item>
            <title>Dide–Botcazo syndrome due to bilateral occlusion of posterior cerebral artery</title>
            <link>http://www.medworm.com/index.php?rid=3016361&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fvh68jg5133m78r43%2F</link>
            <description>We report a case of a man who acutely presented confusion and cortical blindness. The cerebral angiography
 demonstrated bilateral occlusion of posterior cerebral artery (PCA). Sequential intravenous (IV) and intra-arterial (IA) thrombolysis
 were ineffective and the patient developed a complete Dide–Botcazo syndrome.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0179-7Authors
		Manuel Cappellari, Azienda Ospedaliera-Universitaria Dipartimento di Scienze Neurologiche e della Visione Verona ItalyGiampaolo Tomelleri, Azienda Ospedaliera-Universitaria Unità Operativa di Neurologia Verona ItalyAlessandro Di Matteo, Azienda Ospedaliera-Universitaria Dipartimento di Scienze Neurologiche e della Visione Verona ItalyMonica Carletti, Azienda Ospedaliera-Universitaria ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3016361</comments>
            <pubDate>Thu, 19 Nov 2009 07:47:10 +0100</pubDate>
            <guid isPermaLink="false">3016361</guid>        </item>
        <item>
            <title>Diabetic muscle infarction in a patient with acute embolic stroke</title>
            <link>http://www.medworm.com/index.php?rid=3016364&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu485t566v4pr8144%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Diabetic mellitus (DM) has many well-known complications. However, there is one rare complication, diabetic muscle infarction
 (DMI), which is usually under diagnosed. Hereby, we present a 53-year-old Chinese man with a history of DM, hypertension and
 atrial fibrillation. He had acute onset of severe left lower leg pain and swelling with difficulty in walking 4&amp;nbsp;days before
 admission. Physical examination revealed non-pitting and non-erythematous swelling with cold sensation of the left medial
 calf muscles. Magnetic resonance image (MRI) showed homogenous high signal changes in the calf muscles on T2 images, which
 indicated DMI. After anticoagulation treatment, the patient had a fair recovery within 4&amp;nbsp;weeks and he could walk by himself
 thereafter. DMI is a...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3016364</comments>
            <pubDate>Thu, 19 Nov 2009 07:47:09 +0100</pubDate>
            <guid isPermaLink="false">3016364</guid>        </item>
        <item>
            <title>The FRAGAMP study: environmental and genetic factors in Parkinson’s disease, methods and clinical features</title>
            <link>http://www.medworm.com/index.php?rid=3016363&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fug383g394u290023%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The Fattori di Rischio Ambientali e Genetici Associati alla Malattia di Parkinson (FRAGAMP) study is a multicenter case–control
 study carried out to evaluate the possible role of environmental and genetic factors in Parkinson’s disease (PD). Cases and
 controls were enrolled from five Movement Disorder centers in Central-Southern Italy. PD was diagnosed according to Gelb’s
 criteria while the control groups consisted of the spouses of the enrolled patients or of healthy controls matched by age
 and area of residence. Cases and controls underwent a standardised questionnaire and a blood sample was taken for molecular
 analyses. At the end of the study 585 cases and 481 control subjects (287 spouse-controls and 194 generic-controls) were enrolled.
 Patients had a H...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3016363</comments>
            <pubDate>Thu, 19 Nov 2009 07:47:09 +0100</pubDate>
            <guid isPermaLink="false">3016363</guid>        </item>
        <item>
            <title>The effect of l-Dopa administration on pursuit ocular movements in suspected Parkinson’s disease</title>
            <link>http://www.medworm.com/index.php?rid=3016362&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F46gg34379646u6k2%2F</link>
            <description>The objective of this study is to evaluate pursuit ocular movements (POM) by using a vision-based non-intrusive eye tracker,
 in patients with suspected Parkinson’s disease (PD), before and after l-Dopa administration. We studied ten patients with suspected diagnosis of idiopathic PD. We compared POM values to those of
 a group of normal controls (NC), and evaluated them before and after l-Dopa administration. Unified Parkinson’s Disease Rating Scale (UPDRS) motor subscores improved significantly (p&amp;nbsp;=&amp;nbsp;0.001). At baseline, values of POM were lower in suspected PD patients than in NC (p&amp;nbsp;=&amp;nbsp;0.01). One hour after l-Dopa administration, POM values correlated with UPDRS motor subscore (p&amp;nbsp;=&amp;nbsp;0.01). We used a recent method, a new vision-based non-intrusive eye track...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3016362</comments>
            <pubDate>Thu, 19 Nov 2009 07:47:09 +0100</pubDate>
            <guid isPermaLink="false">3016362</guid>        </item>
        <item>
            <title>Factors affecting the retrieval of famous names</title>
            <link>http://www.medworm.com/index.php?rid=2986984&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp33444m251513364%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Tests of famous faces are used to study language and memory. Yet, the effect of stimulus properties on performance has not
 been fully investigated. To identify factors influencing proper name retrieval and to probe stimulus-specific parameters within
 proper name lexicon, we analysed the results obtained by 300 healthy participants on a test of famous faces that includes
 74 personalities. A factor analysis yielded five main factors that were characterized by language (national or foreign names),
 epoch of peak popularity (current, recent or past) and occupation (politicians, entertainment and sports) of the personalities.
 Multiple regression analysis showed that participants’ education, age and gender accounted for 10–32% of the variance in factor
 scores. These ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2986984</comments>
            <pubDate>Wed, 11 Nov 2009 06:57:11 +0100</pubDate>
            <guid isPermaLink="false">2986984</guid>        </item>
        <item>
            <title>Heterogeneous seizure manifestations in Hypomelanosis of Ito: report of four new cases and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=2982996&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F08623067h0x75x25%2F</link>
            <description>We report
 on four new HI patients presenting with heterogeneous seizure manifestations and we review the literature concerning epileptic
 seizures in HI. At one extreme, there are patients with generalized seizures well controlled by drug treatment, whereas at
 the opposite there are patients with severe, often pharmacoresistant, focal seizures. The genetic substrate for HI syndrome
 is not homogenous and only partially understood. Further researches are required to shed light on the pathogenesis of HI phenotypes.
 
	Content Type Journal ArticleCategory Review ArticleDOI 10.1007/s10072-009-0160-5Authors
		Komi Assogba, Centre Saint-Paul, Hôpital Henri Gastaut Marseille FranceEdoardo Ferlazzo, IRCCS Centro Neurolesi “Bonino Pulejo” Messina ItalyPasquale Striano, University of Genoa Mu...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2982996</comments>
            <pubDate>Tue, 10 Nov 2009 08:08:58 +0100</pubDate>
            <guid isPermaLink="false">2982996</guid>        </item>
        <item>
            <title>Borrelia burgdorferi, a great chameleon: know it to recognize it!</title>
            <link>http://www.medworm.com/index.php?rid=2971562&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp72x6156241pp580%2F</link>
            <description>We describe a clinical case of neuroborreliosis that occurred in the absence of classical
 erythema migrans or arthralgia. Magnetic resonance imaging findings compatible with simil-vasculitis and demyelinating lesions
 associated with the presence of anti-B. burgdorferi antibodies in the plasma or cerebrospinal liquid is an indication for antimicrobial treatment against B. burgdorferi. An early diagnosis and a prompt establishment of an adequate antibiotic treatment is needed for a successful recovery.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0175-yAuthors
		Iolanda Santino, Sapienza University of Rome Department of Public Health Sciences P.le Aldo Moro, 5 00185 Rome ItalyPaola Comite, Sapienza University of Rome Department of Experimental Medicine and Path...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2971562</comments>
            <pubDate>Fri, 06 Nov 2009 06:47:59 +0100</pubDate>
            <guid isPermaLink="false">2971562</guid>        </item>
        <item>
            <title>Treatment of multiple sclerosis: role of natalizumab</title>
            <link>http://www.medworm.com/index.php?rid=2961216&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft274u7824n32t621%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The results on relapse rate and disease progression of available drugs for multiple sclerosis are shown, as well as their
 most relevant side effects. Results from pivotal and long-term follw-up studies support the efficacy and safety of intererons
 and glatiramer acetate. The treatment with mitoxantrone is limited by the occurrence of infertility, cardiotoxicy and leukaemia.
 Efficacy and tolerability of natalizumab are undisputable, compared to other drugs. Risks related to its treatment are PML,
 opportunistic infections, hepatotoxicity, melanoma, and their occurrence needs to be more exactly assessed by post-marketing
 surveillance. The principles of induction versus escalating therapy are also discussed. The final therapeutic decision is
 based on the evaluation of...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2961216</comments>
            <pubDate>Tue, 03 Nov 2009 02:11:42 +0100</pubDate>
            <guid isPermaLink="false">2961216</guid>        </item>
        <item>
            <title>Autologous haematopoietic stem-cell transplantation in multiple sclerosis: benefits and risks</title>
            <link>http://www.medworm.com/index.php?rid=2961217&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj23t7331x0120852%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Autologous haematopoietic stem-cell transplantation has been evaluated over the last years as a possible new therapeutic strategy
 in severe forms of multiple sclerosis unresponsive to the approved therapies. Up to now, more than 400 patients have been
 treated and numerous are the phase I and phase II studies which addressed the feasibility of this treatment, the efficacy,
 side effects and transplant-related mortality. The clinical response is strongly related to the intensity of the conditioning
 regimen utilized as well as to the phase of the disease course in which the therapy is carried out. Rapidly evolving multiple
 sclerosis with a relapsing–remitting clinical course and MRI signs of activity are the cases that can take more advantage.
 The risk of mortality,...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2961217</comments>
            <pubDate>Tue, 03 Nov 2009 02:11:32 +0100</pubDate>
            <guid isPermaLink="false">2961217</guid>        </item>
        <item>
            <title>Mitoxantrone: benefits and risks in multiple sclerosis patients</title>
            <link>http://www.medworm.com/index.php?rid=2961218&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa5l657n870068090%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Mitoxantrone (MTX) is a synthetic antineoplastic cytotoxic drug, active both on proliferative and non-proliferative cells.
 The efficacy of MTX has been suggested by many open-label or observational studies and demonstrated in four randomized controlled
 clinical trials (RCTs). It is indicated for reducing neurological disability and the frequency of clinical relapses in patients
 with progressive relapsing and worsening relapsing–remitting MS patients. The short-term most frequent adverse events observed
 in RCTs have been nausea/vomiting, alopecia, an increased risk of urinary and respiratory tract infections, phlebitis, transitory
 leukopenia, amenorrhea in female patients and infertility. However, the most serious risks of the drug are represented by
 potential ca...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2961218</comments>
            <pubDate>Tue, 03 Nov 2009 02:11:23 +0100</pubDate>
            <guid isPermaLink="false">2961218</guid>        </item>
        <item>
            <title>Safety profile of Tysabri: international risk management plan</title>
            <link>http://www.medworm.com/index.php?rid=2961219&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F20315887440231k6%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Therapeutic monoclonal antibodies are potent new tools for a molecular targeted approach to modify the course of multiple
 sclerosis (MS). Natalizumab is a monoclonal antibody targeted against alpha-4 integrin that has proved to be very effective
 in the treatment of MS. It is well tolerated, although severe side effects have been reported that have conditioned its use
 as a second-line drug for the treatment of MS. The clinical benefit of natalizumab should be weighed carefully against the
 potential risk of serious adverse events. Therefore, risk management plans have already been developed in order to prevent
 or minimise risks relating to natalizumab. Data so far obtained from these observational programs confirm the already demonstrated
 risk-benefit profile of nat...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2961219</comments>
            <pubDate>Tue, 03 Nov 2009 02:11:13 +0100</pubDate>
            <guid isPermaLink="false">2961219</guid>        </item>
        <item>
            <title>Cyclophosphamide as second-line therapy in multiple sclerosis: benefits and risks</title>
            <link>http://www.medworm.com/index.php?rid=2961220&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr21686723h987156%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cyclophosphamide (Cy) is an alkylating agent used over the past 40&amp;nbsp;years to halt rapidly progressive forms of multiple sclerosis
 (MS). High doses of Cy produce marked immunosuppression and an anti-inflammatory immune deviation. Cy is most effective in
 young patients, with very active MS (frequent relapses, rapid accumulation of disability, and gad+ lesions on brain MRI).
 Monthly intravenous pulses of Cy for 1&amp;nbsp;year, followed by bimonthly pulses for the second year are a well-tolerated protocol
 in MS. Most side effects (mild alopecia, nausea and vomiting, and cystitis) are transient, dose dependent, and reversible.
 Permanent amenorrhoea and bladder cancer have rarely been described. As second-line therapy, Cy can be used in non-responders
 to IFN-β or glat...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2961220</comments>
            <pubDate>Tue, 03 Nov 2009 02:11:04 +0100</pubDate>
            <guid isPermaLink="false">2961220</guid>        </item>
        <item>
            <title>New oral drugs for multiple sclerosis</title>
            <link>http://www.medworm.com/index.php?rid=2961221&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh741712338047161%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Disease-modifying treatments are now available in relapsing–remitting and secondary progressive multiple sclerosis (MS), and
 their beneficial effects have been shown in several clinical studies. However, as these treatments are only partially effective
 in halting the MS disease process and are frequently associated with side effects and suboptimal patient adherence, new oral
 therapeutic approaches are warranted. This review focuses on advances in current and novel oral treatment approaches for MS.
 Several pivotal reports have provided promising results for new oral therapies evaluating the safety and efficacy of new agents
 including fingolimod, fumaric acid, cladribine, teriflunomide and laquinimod.
 
	Content Type Journal ArticleCategory MS TreatmentDOI 10.1007/...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2961221</comments>
            <pubDate>Tue, 03 Nov 2009 02:10:54 +0100</pubDate>
            <guid isPermaLink="false">2961221</guid>        </item>
        <item>
            <title>The pharmacovigilance program on natalizumab in Italy: 2 years of experience</title>
            <link>http://www.medworm.com/index.php?rid=3098450&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F98v05q2wm3u114qg%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;At the end of 2006 a country-based surveillance program on natalizumab therapy in multiple sclerosis was settled in Italy
 by a collaborative effort of the Italian Drug Agency (AIFA) and a group of experts and neurologists appointed by the National
 Society of Neurology (SIN). After 2&amp;nbsp;years, 1,818 patients are registered in the database. The majority of cases (88.6%) failed
 the therapy with beta interferon or glatiramer acetate and had relapses or accumulated disability during immunomodulating
 treatment, while 11.4% of patients enrolled in the surveillance study were not previously treated with immunomodulating therapies
 and had a rapidly evolving clinical course. Almost 10% of the patients treated with natalizumab interrupted, for various different
 reasons, th...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3098450</comments>
            <pubDate>Tue, 03 Nov 2009 02:10:45 +0100</pubDate>
            <guid isPermaLink="false">3098450</guid>        </item>
        <item>
            <title>The pharmacovigilance program on natalizumab in Italy: 2 years of experience</title>
            <link>http://www.medworm.com/index.php?rid=2961222&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F98v05q2wm3u114qg%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;At the end of 2006 a country-based surveillance program on natalizumab therapy in multiple sclerosis was settled in Italy
 by a collaborative effort of the Italian Drug Agency (AIFA) and a group of experts and neurologists appointed by the National
 Society of Neurology (SIN). After 2&amp;nbsp;years, 1,818 patients are registered in the database. The majority of cases (88.6%) failed
 the therapy with beta interferon or glatiramer acetate and had relapses or accumulated disability during immunomodulating
 treatment, while 11.4% of patients enrolled in the surveillance study were not previously treated with immunomodulating therapies
 and had a rapidly evolving clinical course. Almost 10% of the patients treated with natalizumab interrupted, for various different
 reasons, th...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2961222</comments>
            <pubDate>Tue, 03 Nov 2009 02:10:45 +0100</pubDate>
            <guid isPermaLink="false">2961222</guid>        </item>
        <item>
            <title>Interleukin-1B and interleukin-1 receptor antagonist gene polymorphisms in Greek multiple sclerosis (MS) patients with bout-onset MS</title>
            <link>http://www.medworm.com/index.php?rid=2947979&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj5mvv2hr62620647%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We investigated the association of specific polymorphisms of the interleukin IL-1b (AvaI −511 and TaqI +3,953) and IL-1 receptor antagonist (IL-1RN) (a variable number of tandem repeats; VNTR) genes with both the susceptibility
 to and the clinical characteristics in Greek multiple sclerosis (MS) patients cohort with bout-onset. Genotypes were determined
 from 351 patients with clinically definite MS and 375 age- and sex-matched healthy controls. Our results showed no significant
 differences in the distribution of these polymorphisms between MS patients and controls. Furthermore, stratification for clinical
 characteristics, such as age at disease onset, clinical course, sex, and severity did not provide significant differences
 between patients and controls. Togethe...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2947979</comments>
            <pubDate>Fri, 30 Oct 2009 07:48:23 +0100</pubDate>
            <guid isPermaLink="false">2947979</guid>        </item>
        <item>
            <title>The existence of phonatory instability in multiple sclerosis: an acoustic and electroglottographic study</title>
            <link>http://www.medworm.com/index.php?rid=2947981&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh1nn958075787qg6%2F</link>
            <description>The objective of the study was to investigate the phonatory function
 in MS patients using objective measures. The speech of 64 MS patients and 64 pair-matched controls was recorded and analyzed
 using electroglottography, a physiological method that measures the electrical conductance during the opening and closing
 phases of the vibrating vocal folds. Electroglottographic parameters were correlated with clinical and MRI features. Most
 of the variables that have been used for the analysis of voice (vocal jitter P&amp;nbsp;=&amp;nbsp;0.041, standard deviation of the average fundamental frequency P&amp;nbsp;=&amp;nbsp;0.018, and the mean fundamental frequency of the vibrating vocal folds P&amp;nbsp;=&amp;nbsp;0.025) differentiated the MS group from the control group. Phonatory function is impaired in MS patients,...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2947981</comments>
            <pubDate>Fri, 30 Oct 2009 07:48:22 +0100</pubDate>
            <guid isPermaLink="false">2947981</guid>        </item>
        <item>
            <title>Central pontine and extrapontine myelinolysis despite careful correction of hyponatremia: clinical and neuropathological findings of a case</title>
            <link>http://www.medworm.com/index.php?rid=2947980&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F27638p2800526t7p%2F</link>
            <description>We report clinical, radiological and pathological findings in a patient with central pontine and extrapontine myelinolysis.
 The patient was a 61-year-old woman who had a radical mastectomy for breast cancer. Based on clinical evidence, acute hyponatremia
 had set in only a few days before onset of symptoms. The patient’s disease progressed in two stages and became more severe
 during slow hyponatremia correction after 9&amp;nbsp;days from onset. Diffusion MRI provided early evidence of neurological lesions.
 In spite of a therapeutic attempt, the patient died unexpectedly 18&amp;nbsp;days after onset of her neurological disease due to massive
 pulmonary embolism. Histologically, our findings confirmed that the major features of central pontine myelinolysis in the
 acute stage are demyelination,...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2947980</comments>
            <pubDate>Fri, 30 Oct 2009 07:48:22 +0100</pubDate>
            <guid isPermaLink="false">2947980</guid>        </item>
        <item>
            <title>Unexplained dyspnea in an old patient with recurrent stroke: platypnea–orthodeoxia syndrome and evidence of patent foramen ovale</title>
            <link>http://www.medworm.com/index.php?rid=2947982&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9284001867224048%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Platypnea–orthodeoxia is a syndrome characterized by dyspnea and hypoxemia in orthostatism relieved by supine position. This
 phenomenon is frequently associated with interatrial communication, mainly patent foramen ovale. The association of platypnea–orthodeoxia
 syndrome with recurrent stroke and patent foramen ovale is extremely uncommon. A 73-year-old woman experienced recurrent attacks
 of dyspnea after an ischemic stroke. Arterial blood gas analysis changes in upright and supine position confirmed the diagnosis
 of platypnea–orthodeoxia syndrome. Contrast-enhanced transthoracic echocardiography showed patent foramen ovale with atrial
 septal aneurysm and right-to-left shunt. Percutaneous closure of patent foramen ovale led to stabilization of blood oxygen
 s...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2947982</comments>
            <pubDate>Fri, 30 Oct 2009 07:48:21 +0100</pubDate>
            <guid isPermaLink="false">2947982</guid>        </item>
        <item>
            <title>Cystic neurohypophysial germinoma associated with moyamoya disease</title>
            <link>http://www.medworm.com/index.php?rid=2947983&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq5h85t5453v4135t%2F</link>
            <description>This report describes a case of
 a cystic neurohypophysial germinoma associated with moyamoya disease. A 15-year-old girl with central diabetes insipidus was
 admitted to the hospital. Radiological examination revealed a suprasellar tumor and moyamoya disease. Surgery and pathological
 study confirmed pure germinoma. After the patient was treated with radiation and chemotherapy, the tumor was controlled without
 any effect on the moyamoya vessels. This report describes a rare incidental combination of moyamoya disease and a suprasellar
 germinoma. In the management of such cases, physicians should be aware of the symptoms, course, and natural history of both
 diseases and the effects and side effects of each type of therapy.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s1...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2947983</comments>
            <pubDate>Fri, 30 Oct 2009 07:48:20 +0100</pubDate>
            <guid isPermaLink="false">2947983</guid>        </item>
        <item>
            <title>Late-onset choreoathetotic syndrome following heart surgery</title>
            <link>http://www.medworm.com/index.php?rid=2936699&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn034540175413156%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Choreoathetotic syndromes are frequently observed in children after congenital cardiopathy surgery. To report the case of
 an adult patient who developed a choreoathetotic syndrome after cardiac operation, probably related to a transitory hypometabolism
 of basal ganglia. A 52-year-old patient underwent heart surgery under circulatory arrest and deep hypothermia, for type III
 dissecting thoracic aorta aneurysm. Two weeks later she developed an acute choreic syndrome. The positron emission tomography
 using fluorodeoxyglucose (FDGC-PET) showed a bilateral hypometabolism of basal ganglia. After haloperidol administration,
 choreic syndrome improved and 6&amp;nbsp;months later FDGC-PET was normal. Choreoathetosis has been described as a rare complication
 after heart surgery....</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2936699</comments>
            <pubDate>Tue, 27 Oct 2009 18:23:05 +0100</pubDate>
            <guid isPermaLink="false">2936699</guid>        </item>
        <item>
            <title>Dementia and capsular genu ischemia in patients with severe bacterial meningitis</title>
            <link>http://www.medworm.com/index.php?rid=2906645&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fpp41348451tkt656%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Infarction in the genu of the internal capsule causes dementia that is characterized by abulia, lethargy and memory loss without
 obvious motor palsy (capsular genu syndrome). We found infarction or decreased cerebral blood flow in the genu of the internal
 capsule in 6 of 13 patients with severe bacterial meningitis. Four of these six patients developed post-meningitis dementia,
 characterized by abulia, lethargy, and memory loss. Of 24 patients with viral meningitis, none developed capsular genu ischemia
 or post-meningitis dementia. In patients with severe bacterial meningitis, capsular genu ischemia may play some role in the
 development of post-meningitis dementia. In patients with viral meningitis, absence of such ischemia may explain, at least
 in a part, the rar...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2906645</comments>
            <pubDate>Fri, 16 Oct 2009 17:56:45 +0100</pubDate>
            <guid isPermaLink="false">2906645</guid>        </item>
        <item>
            <title>The first case history of multiple sclerosis: Augustus d’Esté (1794–1848)</title>
            <link>http://www.medworm.com/index.php?rid=2906646&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx3v53k896261w427%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The personal diary of Sir Augustus d’Esté, born 1794 grandson of King George III of England, reveals a medical history strongly
 suggesting that Augustus suffered from multiple sclerosis (MS). It could well be the first record of a person having this
 disease. Charcot coined the term sclérose en plaques 20&amp;nbsp;years after the death of this patient in 1848. The onset of this man’s
 MS seems to have been in 1822 with bilateral optic neuritis, the disease gradually developing in the classic manner with bouts
 derived from different loci in the central nervous system and eventually a secondary progressive form with paraparesis, sphincter
 incontinence, urinary problems and impotence. In 1941, Firth highlighted the case of Augustus d’Esté and later wrote a descript...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2906646</comments>
            <pubDate>Fri, 16 Oct 2009 17:56:44 +0100</pubDate>
            <guid isPermaLink="false">2906646</guid>        </item>
        <item>
            <title>Alzheimer’s disease and endothelial dysfunction</title>
            <link>http://www.medworm.com/index.php?rid=2906647&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn8237741u9708174%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Recent studies suggest strong interactions between cerebrovascular and Alzheimer’s disease (AD) pathology. These conditions
 share common risk factors and individuals having both frequently show greater cognitive impairment than those affected by
 only one disease. Many studies point to early vascular dysregulations in AD. The exchange between vascular and neural cells
 occurs through mechanisms not completely understood, involving interactions among endothelial, glial, neuronal and smooth
 muscle cells within the neurovascular unit. Studies suggest that the dysregulation of the unit is likely associated with hypertension
 and other systemic diseases. Associations between hypertension and cognitive decline are not established, but other variables
 associated with hype...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2906647</comments>
            <pubDate>Fri, 16 Oct 2009 17:56:43 +0100</pubDate>
            <guid isPermaLink="false">2906647</guid>        </item>
        <item>
            <title>Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients</title>
            <link>http://www.medworm.com/index.php?rid=2906648&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd40n6517384850r7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We prospectively followed-up 32 pediatric patients with cerebral cavernomas (CCs) to better define surgical indications in
 this population. Three groups of patients were identified: (a) children with macrohemorrhage (21 patients, 65.6%), (b) children
 with localized or diffuse headache (6 patients, 18.8%) and (c) children with epilepsy (5 patients, 15.6%). Surgery was performed
 in 28 out of the 32 (87.5%) subjects. New transient post-operative neurological deficits were observed in two children. One
 child developed a post-operative hematoma. At a median follow-up of 4&amp;nbsp;years (range 1–11&amp;nbsp;years), 22 out of the 28 (78.6%) operated
 patients were in good conditions. All operated subjects with epilepsy were seizure-free. We confirm the high risk of macrohemorrh...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2906648</comments>
            <pubDate>Fri, 16 Oct 2009 09:21:02 +0100</pubDate>
            <guid isPermaLink="false">2906648</guid>        </item>
        <item>
            <title>Utilization and outcome of thrombolytic therapy for acute stroke in Pakistan</title>
            <link>http://www.medworm.com/index.php?rid=2880598&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbl2k60k674387378%2F</link>
            <description>In conclusion, the utilization of thrombolytic
 therapy is low and complication rate is high. Interventions for training physicians are needed.
 
	Content Type Journal ArticleCategory Brief CommunicationDOI 10.1007/s10072-009-0159-yAuthors
		Mohammad Wasay, Aga Khan University Department of Neurology and Medicine Stadium Road Karachi 74800 PakistanHazim Barohi, Aga Khan University Department of Neurology and Medicine Stadium Road Karachi 74800 PakistanAbdul Malik, Liaquat National Hospital Department of Neurology Karachi PakistanAdnan Yousuf, Aga Khan University Department of Neurology and Medicine Stadium Road Karachi 74800 PakistanSafia Awan, Aga Khan University Department of Neurology and Medicine Stadium Road Karachi 74800 PakistanAyeesha K. Kamal, Aga Khan University Department of Neu...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2880598</comments>
            <pubDate>Fri, 09 Oct 2009 06:16:54 +0100</pubDate>
            <guid isPermaLink="false">2880598</guid>        </item>
        <item>
            <title>Concordance between severity of disease, disability and health-related quality of life in Myasthenia gravis</title>
            <link>http://www.medworm.com/index.php?rid=2880599&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F37256982346711r7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Aim of this study is to verify whether there is concordance between disease’s severity, health-related quality of life (HRQoL)
 and disability in patients with Myasthenia gravis (MG). 102 MG patients were clustered on the basis of HRQoL and disability
 scores into three groups: low disability and low HRQoL decrement (51 patients), intermediate disability and HRQoL decrement
 (28 patients), severe disability and high HRQoL decrement (23 patients). Cross tabulation with symmetric measures (Cramer’s&amp;nbsp;V and Contingency Coefficient) was used to verify the relationships between disease severity groups, based on the Myasthenia
 Gravis Foundation of America (MGFA) criteria, and obtained clusters. Results confirm a significant relationship between MG
 severity groups, HR...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2880599</comments>
            <pubDate>Fri, 09 Oct 2009 06:16:53 +0100</pubDate>
            <guid isPermaLink="false">2880599</guid>        </item>
        <item>
            <title>Familial hemifacial spasm and determinants of late onset</title>
            <link>http://www.medworm.com/index.php?rid=2877913&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1724v58572621534%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The role of hypertension in the late onset of hemifacial spasm (HFS) is evaluated in a family, spanning four generations.
 Magnetic resonance imaging (MRI) and magnetic resonance angiography (MRA) revealed a variable anatomical relationship between
 nervous and vascular structures in the symptomatic cerebello-pontine angle. In one case, showing neurovascular conflict (NVC),
 microvascular surgical decompression was followed by clinical resolution of HFS. Neuroimaging suggesting NVC was found in
 all symptomatic patients of the last two generations and in three younger subjects not affected by HFS. As a determinant for
 the late development of clinical expression is reviewed the role of arterial hypertension, detected few years before HFS appearing
 in all symptomatic su...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2877913</comments>
            <pubDate>Thu, 08 Oct 2009 07:01:34 +0100</pubDate>
            <guid isPermaLink="false">2877913</guid>        </item>
        <item>
            <title>Leprosy: report of a case with severe peripheral neuropathy</title>
            <link>http://www.medworm.com/index.php?rid=2877912&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F968u224442h61272%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Leprosy (Hansen’s disease) is a chronic granulomatous infectious disease, caused by Mycobacterium leprae, with cutaneous and neurological manifestations. Leprosy is very rare in Europe but some cases are reported, especially among
 people coming from endemic areas. Here, we report a case of Hansen’s disease and emphasize the importance of a prompt diagnosis
 and treatment also in non-endemic areas.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0152-5Authors
		Paolo Aridon, University of Palermo Dipartimento Universitario di Neuroscienze Cliniche (DiNeC) Via Gaetano La Loggia 1 90129 Palermo ItalyPaolo Ragonese, University of Palermo Dipartimento Universitario di Neuroscienze Cliniche (DiNeC) Via Gaetano La Loggia 1 90129 Palermo ItalyMari...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2877912</comments>
            <pubDate>Thu, 08 Oct 2009 07:01:34 +0100</pubDate>
            <guid isPermaLink="false">2877912</guid>        </item>
        <item>
            <title>Reversible posterior leukoencephalopathy syndrome in childhood: report of nine cases and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=2873922&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv674mmv11n3n6h0k%2F</link>
            <description>We presented nine patients with RPLS who had primary diagnoses such as acute post-streptococcal glomerulonephritis,
 idiopathic hypertension, the performing of intravenous immunoglobulin for infection with crescentic glomerulonephritis, erythrocyte
 transfusion for severe iron deficiency, l-asparaginase treatment for acute lymphoblastic leukemia and performing of granulocyte-colony stimulating factor for ulcerative
 colitis due to neutropenia. Early recognition of RPLS as complication during different diseases and therapy in childhood may
 facilitate precise diagnosis and appropriate treatment.
 
	Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s10072-009-0158-zAuthors
		Hakan Gümüş, Kayseri Education and Research Hospital Department of Pediatric Neurology Talas Kayseri...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2873922</comments>
            <pubDate>Wed, 07 Oct 2009 07:40:31 +0100</pubDate>
            <guid isPermaLink="false">2873922</guid>        </item>
        <item>
            <title>Cerebral venous thrombosis with dural arteriovenous fistulas and antiphospholipid syndrome: a case report</title>
            <link>http://www.medworm.com/index.php?rid=2870444&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2564125614267w55%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorDOI 10.1007/s10072-009-0166-zAuthors
		Yasuo Miki, Aomori Prefectural Central Hospital Department of Neurology Higashi Tsukurimichi 2-1-1 Aomori JapanMasahiko Tomiyama, Aomori Prefectural Central Hospital Department of Neurology Higashi Tsukurimichi 2-1-1 Aomori JapanAkira Arai, Aomori Prefectural Central Hospital Department of Neurology Higashi Tsukurimichi 2-1-1 Aomori JapanTamaki Kimura, Aomori Prefectural Central Hospital Department of Neurology Higashi Tsukurimichi 2-1-1 Aomori JapanChieko Suzuki, Aomori Prefectural Central Hospital Department of Neurology Higashi Tsukurimichi 2-1-1 Aomori JapanJin-ichi Nunomura, Aomori Prefectural Central Hospital Department of Neurology Higashi Tsukurimichi 2-1-1 Aomori JapanHiroshi Midorika...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2870444</comments>
            <pubDate>Tue, 06 Oct 2009 12:53:16 +0100</pubDate>
            <guid isPermaLink="false">2870444</guid>        </item>
        <item>
            <title>Psychiatric symptoms in Parkinson’s disease assessed with the SCL-90R self-reported questionnaire</title>
            <link>http://www.medworm.com/index.php?rid=2870446&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F16335746x0841858%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The frequency of psychopathological symptoms in patients with Parkinson’s disease (PD) is often underestimated because of
 the lack of comprehensive evaluation tools. A total of 486 consecutive non-demented PD patients completed the Symptom Checklist
 90 Revised (SCL-90R) self-reported questionnaire, a validated tool for the assessment of psychopathological symptoms on nine
 dimensions. Somatization, depression, anxiety and obsessive–compulsive behaviors were reported by nearly half of the PD patients.
 They were more likely to occur in females. Disease-related factors such as duration, severity and daily dosages, but not type
 of dopaminergic medications, were associated with the occurrence of these symptoms. Psychopathological features are frequent
 in PD and thei...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2870446</comments>
            <pubDate>Tue, 06 Oct 2009 12:53:15 +0100</pubDate>
            <guid isPermaLink="false">2870446</guid>        </item>
        <item>
            <title>Thoracic extradural haematoma after epidural anaesthesia</title>
            <link>http://www.medworm.com/index.php?rid=2870445&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9277n255j28j1232%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The administration of analgesics to the thoracic spine is established practice in the operating room, minimizing the need
 for systemic anaesthetic administration during thoracic surgery. Complications arising from thoracic epidural anaesthesia
 are uncommon but potentially disastrous. Here, we report the case of a 43-year-old woman who developed a thoracic epidural
 haematoma with paraplegia a few hours after the removal of an epidural catheter. The patient underwent emergency thoracic
 laminectomy and clot evacuation. After a 4&amp;nbsp;months period, there was almost complete neurological recovery. Epidural haematoma
 is a rare complication that must be heeded and urgently treated in case of clinical deterioration after the epidural analgesia.
 
	Content Type Journal Art...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2870445</comments>
            <pubDate>Tue, 06 Oct 2009 12:53:15 +0100</pubDate>
            <guid isPermaLink="false">2870445</guid>        </item>
        <item>
            <title>Isolated ataxia after pure left insular cortex infarction</title>
            <link>http://www.medworm.com/index.php?rid=2870447&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg544v354155x368r%2F</link>
            <description>In conclusions, left insular cortex
 lesions should be considered in the differential diagnosis of isolated truncal ataxia.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0164-1Authors
		Li-Min Liou, Kaohsiung Medical University Department of Neurology, Kaohsiung Municipal Hsiao-kang Hospital Kaohsiung TaiwanYuh-Cherng Guo, Kaohsiung Medical University Department of Neurology, Kaohsiung Municipal Hsiao-kang Hospital Kaohsiung TaiwanChiou-Lian Lai, Kaohsiung Medical University Department of and Master’s Program in Neurology, Faculty of Medicine, College of Medicine Kaohsiung TaiwanChin-Ling Tsai, Kaohsiung Medical University Department of Neurology, Kaohsiung Municipal Hsiao-kang Hospital Kaohsiung TaiwanGim-Thean Khor, Kaohsiung Medical University Department of...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2870447</comments>
            <pubDate>Tue, 06 Oct 2009 12:53:13 +0100</pubDate>
            <guid isPermaLink="false">2870447</guid>        </item>
        <item>
            <title>Cerebellar degeneration and ocular myasthenia gravis in a patient with recurring ovarian carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=2870449&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff333780577755561%2F</link>
            <description>We report a patient with history of ovarian carcinoma that presented with ptosis, diplopia and gait ataxia. Neurophysiological
 examination and laboratory tests revealed the presence of MG and PCD. An integrated FDG-PET/contrast-enhanced CT scan showed
 tumor recurrence. This is to the best of our knowledge the first association of MG and PCD with recurring ovarian carcinoma.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0154-3Authors
		Pietro Caliandro, Università Cattolica del Sacro Cuore Neurology Department, Istituto di Neurologia Pol. “A: Gemelli” Largo Gemelli 8 00168 Rome ItalyMarco Luigetti, Università Cattolica del Sacro Cuore Neurology Department, Istituto di Neurologia Pol. “A: Gemelli” Largo Gemelli 8 00168 Rome ItalyEnzo Ricci, Università...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2870449</comments>
            <pubDate>Tue, 06 Oct 2009 12:53:11 +0100</pubDate>
            <guid isPermaLink="false">2870449</guid>        </item>
        <item>
            <title>Advanced age as a contraindication to microvascular decompression for drug-resistant trigeminal neuralgia: evidence of prejudice?</title>
            <link>http://www.medworm.com/index.php?rid=2870448&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyk775422956178j4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Due to the alleged higher risk of complications of microvascular decompression for trigeminal neuralgia in elderly we evaluated
 its age-related results. A retrospective analysis of clinical outcome and complications was performed in 476 patients affected
 by drug-resistant trigeminal neuralgia who underwent microvascular decompression. As much as 117 patients older than 65&amp;nbsp;years
 (Group 1) and 359 under the age of 65 (Group 2) were followed-up for a period of 7–138&amp;nbsp;months. Pain relief was complete without
 medication in 84.5% in Group 1. Morbidity included slight trigeminal hypoesthesia in 5.8%; severe hearing loss in 0.9%; CSF
 leakage in 4.2%; transient diplopia in 3.4%; and posterior fossa subdural hematoma in 0.8% of these patients. Mortality was
 null....</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2870448</comments>
            <pubDate>Tue, 06 Oct 2009 12:53:11 +0100</pubDate>
            <guid isPermaLink="false">2870448</guid>        </item>
        <item>
            <title>A case report of cranial polyneuropathy in Behcet’s disease</title>
            <link>http://www.medworm.com/index.php?rid=2870450&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F78l5736871muupj4%2F</link>
            <description>We report a 19-year-old man with BD who presented
 with cranial polyneuropathy secondary to aseptic meningitis. He made a gradual though incomplete recovery with steroid therapy.
 Cranial polyneuropathy secondary to meningeal involvement can be a presentation of n-BD, and Behcet’s disease should be a
 consideration in patients with idiopathic cranial polyneuropathy.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0162-3Authors
		Ali Alrefai, Jordan University of Science and Technology (JUST) Department of Neuroscience PO Box 3030 Irbid 22110 JordanKhalid El-Salem, Jordan University of Science and Technology (JUST) Department of Neuroscience PO Box 3030 Irbid 22110 JordanRuba Saadeh, Jordan University of Science and Technology (JUST) Department of Neuroscience PO...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2870450</comments>
            <pubDate>Tue, 06 Oct 2009 12:53:10 +0100</pubDate>
            <guid isPermaLink="false">2870450</guid>        </item>
        <item>
            <title>Harmful effect of kainic acid on brain ischemic damage is not related to duration of status epilepticus</title>
            <link>http://www.medworm.com/index.php?rid=2840616&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr3047k1113436g11%2F</link>
            <description>This study
 indicates that there is dissociation between stopping status epilepticus and modifying its long-term consequences.
 
	Content Type Journal ArticleCategory Brief CommunicationDOI 10.1007/s10072-009-0115-xAuthors
		Henry Hasson, Albert Einstein College of Medicine of Yeshiva University Saul R. Korey Department of Neurology Bronx NY USASamit Malhotra, SUNY Downstate Medical Center Department of Neurology Brooklyn NY USAFilippo S. Giorgi, University of Pisa Section of Neurology, Department of Neuroscience Pisa ItalyDaniel M. Rosenbaum, SUNY Downstate Medical Center Department of Neurology Brooklyn NY USASolomon L. Moshé, Albert Einstein College of Medicine of Yeshiva University Saul R. Korey Department of Neurology Bronx NY USA
	

	
		Journal Neurological SciencesOnline ISSN 1590-...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2840616</comments>
            <pubDate>Fri, 25 Sep 2009 05:48:12 +0100</pubDate>
            <guid isPermaLink="false">2840616</guid>        </item>
        <item>
            <title>Perceptive aspects of visual aura</title>
            <link>http://www.medworm.com/index.php?rid=2835167&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh3180751r4260193%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Visual aura is the most common feature associated with migraine, though it can occur separately. In both cases it often represents
 a dramatic event, especially for patients who experience it for the first time. Besides, its subjective characteristics may
 illuminate on the functional architecture of the visual cortex. Repetitive events of migraine and visual aura have been suggested
 to affect the visual system in the long run, both on the cortical and precortical level. In effect, objective investigation
 of visual functions in patients support the idea that a selective damage does occur, so that more attention to visual examination
 seems to be justified. In this paper, subjective and psychophysical aspects of visual aura are examined, lastly highlighting
 and discus...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2835167</comments>
            <pubDate>Fri, 25 Sep 2009 05:48:12 +0100</pubDate>
            <guid isPermaLink="false">2835167</guid>        </item>
        <item>
            <title>Speech-induced blepharospasm</title>
            <link>http://www.medworm.com/index.php?rid=2840617&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq538633076602955%2F</link>
            <description>We report
 the clinical vignette of two patients manifesting an unusual presentation of primary blepharospasm, specifically triggered
 by voiced speech and associated with an otherwise ‘typical’ presentation of primary adult-onset dystonia in the lower face,
 larynx or upper limb. Speech-induced primary blepharospasm seems a rare occurrence, representing 1.3% of our clinic-based
 series of 149 patients with primary adult-onset primary blepharospasm. In these atypical patients, the feature of speech inducibility
 suggests that the abnormal surrounding inhibition between cortical subregions representing laryngeal and orbicularis oculi
 muscles might underlie dystonic overflow to the orbicularis oculi muscles following the voiced speech.
 
	Content Type Journal ArticleCategory Case Report...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2840617</comments>
            <pubDate>Thu, 24 Sep 2009 16:45:42 +0100</pubDate>
            <guid isPermaLink="false">2840617</guid>        </item>
        <item>
            <title>Progressive necrotic encephalopathy following tacrolimus therapy for liver transplantation</title>
            <link>http://www.medworm.com/index.php?rid=2840618&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy87h7904448221m4%2F</link>
            <description>We describe a 57-year-old man who underwent liver transplantation and was
 started on immunosuppressive therapy with tacrolimus (FK506). Six&amp;nbsp;months later, he started complaining of a progressive motor
 and sensory impairment of the left side, together with cognitive impairment. Brain MRI showed an enlarging lesion of the white
 matter with peripheral contrast enhancement. PET study indicated severe hypometabolism in the right hemisphere and spectroscopic
 MRI showed a peak of choline and relative reduction of other metabolites. Findings of CSF examinations and cultures, serology,
 and molecular techniques were normal. Tacrolimus treatment was stopped. A cerebral biopsy of the lesion showed a sub acute
 necrotizing process. In the following months, cognitive status of the patient tende...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2840618</comments>
            <pubDate>Thu, 24 Sep 2009 16:45:39 +0100</pubDate>
            <guid isPermaLink="false">2840618</guid>        </item>
        <item>
            <title>Dopamine transporter (DAT1) VNTR polymorphism in 12 Indian populations</title>
            <link>http://www.medworm.com/index.php?rid=2840619&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx588777778p26v77%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The dopamine transporter (DAT1) is a membrane spanning protein that binds the neurotransmitter dopamine and performs re-uptake
 of dopamine from the synapse into a neuron. The gene encoding DAT1 consists of 15 exons spanning 60&amp;nbsp;kb on chromosome 5p15.32.
 Several studies have investigated the possible associations between variants in DAT1 gene and psychiatric disorders. The present
 study aimed to determine the distribution of the variable number of tandem repeat (VNTR) polymorphism in the 3′ untranslated
 region of DAT1 in 12 Indian populations. A total of 471 healthy unrelated individuals in 12 Indian populations from 3 linguistic
 groups were included in the present study. The analysis was carried out using PCR and electrophoresis. Overall, 4 alleles
 of the DA...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2840619</comments>
            <pubDate>Thu, 24 Sep 2009 16:45:38 +0100</pubDate>
            <guid isPermaLink="false">2840619</guid>        </item>
        <item>
            <title>Paragangliomas of head and neck: a treatment option with CyberKnife radiosurgery</title>
            <link>http://www.medworm.com/index.php?rid=2833432&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F274641136328j8ul%2F</link>
            <description>In conclusion, CyberKnife radiosurgery appears to be both safe and effective
 in the treatment of skull base paragangliomas. Determining whether long-term complications will arise will require further
 investigation.
 
	Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s10072-009-0138-3Authors
		Livia C. Bianchi, CyberKnife Center CDI Milan ItalyMarcello Marchetti, Fondazione IRCCS Istituto Neurologico Carlo Besta Department of Neurosurgery, Division of Radiotherapy Milan ItalyLorenzo Brait, CyberKnife Center CDI Milan ItalyAchille Bergantin, CyberKnife Center CDI Milan ItalyIda Milanesi, Fondazione IRCCS Istituto Neurologico Carlo Besta Department of Neurosurgery, Division of Radiotherapy Milan ItalyGiovanni Broggi, Fondazione IRCCS Istituto Neurologico Carlo Besta Departme...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2833432</comments>
            <pubDate>Wed, 23 Sep 2009 06:04:10 +0100</pubDate>
            <guid isPermaLink="false">2833432</guid>        </item>
        <item>
            <title>Spinocerebellar ataxia type 11 in the Chinese Han population</title>
            <link>http://www.medworm.com/index.php?rid=2816878&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd0742175wh37n420%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The spinocerebellar ataxias (SCAs) are a clinically and genetically heterogeneous group of neurodegenerative diseases. Researchers
 have recently found that SCA type 11 (SCA11) is associated with mutations in the TTBK2 gene. In our previous work, we performed mutation detection in SCA1, 2, 3, 6, 7, 8, 10, 12, 17 and dentatorubral-pallidoluysian
 atrophy gene in Chinese SCA patients, but the genes responsible for approximately 40% of our patients have not yet been identified.
 To investigate the frequency of SCA11 in Chinese SCA patients, we examined the TTBK2 gene in 68 unrelated probands diagnosed with dominantly inherited ataxia using the denaturing high-performance liquid chromatography
 method. All analyzed samples displayed the normal elution profile, which denoted...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2816878</comments>
            <pubDate>Sat, 19 Sep 2009 05:51:49 +0100</pubDate>
            <guid isPermaLink="false">2816878</guid>        </item>
        <item>
            <title>Muscle carnitine deficiency: adult onset lipid storage myopathy with sensory neuropathy</title>
            <link>http://www.medworm.com/index.php?rid=2816879&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl17x0k632n043146%2F</link>
            <description>We report herein a 29-year-old man with muscle carnitine deficiency who developed not only a lipid storage myopathy, but also
 a severe sensory neuropathy. Oral therapy with levo-carnitine (3&amp;nbsp;g per day) for 3&amp;nbsp;months produced a remarkable improvement
 of the myopathy and sensory neuropathy. Six months later, he remained in good condition under strict dietary control. This
 report emphasizes that severe neuropathy may occur in some patients with muscle carnitine deficiency, and highlights the need
 for the neurologist’s familiarity with those afflicted to achieve optimal clinical management.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0128-5Authors
		Wei Zhang, Fourth Military Medical University Department of Neurology, Tangdu Hospital 710038 Xi’an...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2816879</comments>
            <pubDate>Sat, 19 Sep 2009 05:51:48 +0100</pubDate>
            <guid isPermaLink="false">2816879</guid>        </item>
        <item>
            <title>Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia</title>
            <link>http://www.medworm.com/index.php?rid=2816881&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu4lh83p3p7g12275%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A clinical and molecular overlap between Alzheimer’s disease (AD) and frontotemporal dementia (FTD) has been reported. Presenilins
 have been associated with FTD or with FTD-like phenotype, while mutations in the MAPT gene have been linked to a clinical phenotype of AD. We performed a clinical and genetic examination in two FTD siblings
 and their family tree has been reconstructed. We identified a novel Val75Ala MAPT mutation in one patient and in the other the Arg62His Presenilin2 mutation. The DNA variations identified, defined mutations
 by frequency, per se are not causative of the disease. These mutations, possibly in association with other unknown environmental
 and genetic factors, may contribute to neurodegeneration. In this family, the disease might result f...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2816881</comments>
            <pubDate>Sat, 19 Sep 2009 05:51:47 +0100</pubDate>
            <guid isPermaLink="false">2816881</guid>        </item>
        <item>
            <title>Myeloneuropathy due to copper deficiency: clinical and MRI findings after copper supplementation</title>
            <link>http://www.medworm.com/index.php?rid=2816880&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4811341558760030%2F</link>
            <description>In conclusion, in acquired copper-deficiency-associated myelopathy, correction of blood
 and MRI alterations precedes that of neurological manifestations, which may remain suboptimal.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0126-7Authors
		Laura Bolamperti, Ospedale Maggiore della Carità Clinica Neurologica C.so Mazzini, 18 28100 Novara ItalyMaurizio A. Leone, Ospedale Maggiore della Carità Clinica Neurologica C.so Mazzini, 18 28100 Novara ItalyAlessandro Stecco, Amedeo Avogadro University Department of Radiology Novara ItalyMonica Reggiani, Amedeo Avogadro University Clinica Neurologica Novara ItalyMario Pirisi, Amedeo Avogadro University Clinica Medica Novara ItalyAlessandro Carriero, Amedeo Avogadro University Department of Radiology Novara ItalyFranc...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2816880</comments>
            <pubDate>Sat, 19 Sep 2009 05:51:47 +0100</pubDate>
            <guid isPermaLink="false">2816880</guid>        </item>
        <item>
            <title>Irreversible striatal neuroimaging abnormalities secondary to prolonged, uncontrolled diabetes mellitus in the setting of progressive focal neurological symptoms</title>
            <link>http://www.medworm.com/index.php?rid=2816883&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft6472264n072w3w6%2F</link>
            <description>We report a 56-year-old man with a prolonged, uncontrolled hyperglycemia (HbA1C:
 13.8%) and striatal hyperintensity on T1-weighted MR imaging presenting as reversible focal neurological deficit and irreversible
 neuroimaging abnormalities on the fourth month when blood sugar was under control (HbA1C 6.0&amp;nbsp;mg/dl). We hypothesize that neuroimaging
 abnormalities in our case may be a sequence of an “ischemic insult” caused by prolonged, uncontrolled hyperglycemia. Whether
 the signal abnormalities on neuroimaging studies or the clinical syndrome are reversible (patients with HCHB) or irreversible
 (such as in our case) are based on the degree of ischemic damage.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0127-6Authors
		Chin-Sung Tung, I-Shou University ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2816883</comments>
            <pubDate>Sat, 19 Sep 2009 05:51:46 +0100</pubDate>
            <guid isPermaLink="false">2816883</guid>        </item>
        <item>
            <title>Neuromyotonia in idiopathic hypoparathyroidism</title>
            <link>http://www.medworm.com/index.php?rid=2816882&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F38635053p2015304%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Α 62-year-old man was presented with bilateral cataract, proximal muscle weakness and difficulty in relaxing the hands after
 voluntary contraction. Idiopathic hypoparathyroidism was diagnosed. Electrophysiological study showed spontaneous motor unit
 action potentials, occurring and disappearing abruptly, as duplets, triplets and multiplets, with an intra-burst frequency
 of up to 100&amp;nbsp;Hz and some of them waning in amplitude, findings consistent with neuromyotonia.
 
	Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s10072-009-0140-9Authors
		Thomas Zambelis, University of Athens Department of Neurology, Aeghinition Hospital 74, Vassilissis Sofias Avenue 11528 Athens GreeceDimitrios Licomanos, University of Athens Department of Neurology, Aeghiniti...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2816882</comments>
            <pubDate>Sat, 19 Sep 2009 05:51:46 +0100</pubDate>
            <guid isPermaLink="false">2816882</guid>        </item>
        <item>
            <title>Neurosyphilis in the age of AIDS: clinical and laboratory features</title>
            <link>http://www.medworm.com/index.php?rid=2816885&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F14866m73l1151435%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Neurosyphilis remains to be a challenging diagnostic possibility worldwide. The aim of our study was to identify and report
 the clinical and laboratory profile of neurosyphilis, comparing features of HIV-infected and HIV-negative patients. A retrospective
 investigation of all cases of neurosyphilis, defined as positive VDRL test on cerebrospinal fluid, diagnosed at Hospital das
 Clínicas, Ribeirão Preto School of Medicine between January 1988 and December 2005, was carried out. We identified 35 patients
 with a mean age of 42.1&amp;nbsp;years, 28.6% of them HIV infected and 74.3% of them were male. HIV-infected patients were younger
 (34.6&amp;nbsp;years), presented with a higher frequency of the early forms of neurosyphilis, higher titers of serum VDRL and higher
 mean pro...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2816885</comments>
            <pubDate>Sat, 19 Sep 2009 05:51:42 +0100</pubDate>
            <guid isPermaLink="false">2816885</guid>        </item>
        <item>
            <title>Size frequency distribution of the β-amyloid (aβ) deposits in dementia with Lewy bodies with associated Alzheimer’s disease pathology</title>
            <link>http://www.medworm.com/index.php?rid=2816884&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F987j3431g214640v%2F</link>
            <description>The objective is to study β-amyloid (Aβ) deposition in dementia with Lewy bodies (DLB) with Alzheimer’s disease (AD) pathology
 (DLB/AD). The size frequency distributions of the Aβ deposits were studied and fitted by log-normal and power-law models.
 Patients were ten clinically and pathologically diagnosed DLB/AD cases. Size distributions had a single peak and were positively
 skewed and similar to those described in AD and Down’s syndrome. Size distributions had smaller means in DLB/AD than in AD.
 Log-normal and power-law models were fitted to the size distributions of the classic and diffuse deposits, respectively. Size
 distributions of Aβ deposits were similar in DLB/AD and AD. Size distributions of the diffuse deposits were fitted by a power-law
 model suggesting that aggreg...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2816884</comments>
            <pubDate>Sat, 19 Sep 2009 05:51:42 +0100</pubDate>
            <guid isPermaLink="false">2816884</guid>        </item>
        <item>
            <title>Self-help group and medication overuse headache: preliminary data</title>
            <link>http://www.medworm.com/index.php?rid=2816887&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0v0046214631p9mq%2F</link>
            <description>The objective of the study is to investigate the benefits of joining a self-help group for patients with medication overuse
 headache (MOH). A self-help group is a voluntary gathering of a small number of persons who share a common problem. Little
 is known about support groups for people with chronic non-malignant pain such as MOH. Eight patients with refractory MOH attended
 a self-help group twice a month. During the meetings, patients were asked to focus on their headache experiences. Our data
 showed an increase in resourcefulness in coping with pain and a reduction in cephalalgiophobia. All patients reported general
 benefits in sharing their headache-related problems. No differences were found for headache frequency or analgesic overuse.
 To our knowledge, this is the first report o...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2816887</comments>
            <pubDate>Sat, 19 Sep 2009 05:51:40 +0100</pubDate>
            <guid isPermaLink="false">2816887</guid>        </item>
        <item>
            <title>Effects of treadmill training on walking economy in Parkinson’s disease: a pilot study</title>
            <link>http://www.medworm.com/index.php?rid=2816886&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0723964421r06551%2F</link>
            <description>This study evaluated whether the effects of treadmill training are associated with an improvement of walking economy. Ten
 patients with idiopathic PD underwent treadmill training (30&amp;nbsp;min, three times a week for 4&amp;nbsp;weeks). Walking performance (Τimed
 Up and Go, 6-min and 10-m walking tests) and metabolic function (oxygen uptake, heart and respiratory rate) were evaluated
 before training, at the end of treatment and after 30&amp;nbsp;days with two different graded exercises (treadmill and cycloergometer).
 Training significantly improved walking performance. Oxygen uptake, and heart and respiratory rates were significantly decreased
 only during graded exercise on the treadmill, but not on the cycloergometer. Treadmill training reduces energy expenditure
 during walking in PD, but th...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2816886</comments>
            <pubDate>Sat, 19 Sep 2009 05:51:40 +0100</pubDate>
            <guid isPermaLink="false">2816886</guid>        </item>
        <item>
            <title>Syringomyelia associated with Chiari I malformation</title>
            <link>http://www.medworm.com/index.php?rid=2816889&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx1p17n850330246t%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;An 18-year-old man with progressive paraparesis, thermal hypoesthesia, sweating abnormalities, bladder dysfunction, severe
 orthostatic hypotension, bilateral Babinski sign, underwent a brain MRI scan that showed downward displacement of cerebellar
 tonsils through the foramen magnum, consistent with Chiari I malformation, compression of the brainstem–spinal cord junction,
 and C1–D11 syringomyelia (6.5&amp;nbsp;mm diameter at C2 level) consistent with Chiari I syndrome. Suboccipital craniectomy and duraplasty
 were performed. A C2 partial laminectomy and ablation of posterior arch of the atlas was performed. MRI scans 4&amp;nbsp;days and 1&amp;nbsp;month
 after surgery showed a dramatic syringomyelia reabsorption (2.5 and 1&amp;nbsp;mm, respectively) associated with complete clini...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2816889</comments>
            <pubDate>Sat, 19 Sep 2009 05:51:39 +0100</pubDate>
            <guid isPermaLink="false">2816889</guid>        </item>
        <item>
            <title>Lack of effect of cannabis-based treatment on clinical and laboratory measures in multiple sclerosis</title>
            <link>http://www.medworm.com/index.php?rid=2816888&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp912058082862t75%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The endocannabinoid system (ECS) is involved in the pathophysiology of multiple sclerosis (MS), and relief from pain and spasticity
 has been reported in MS patients self-medicating with marijuana. A cannabis-based medication containing Δ9-tetrahydrocannabinol and cannabidiol (Sativex®) has been approved in some countries for the treatment of MS-associated pain. The effects of this pharmaceutical preparation
 on other clinically relevant aspects of MS pathophysiology, however, are still unclear. In 20 MS patients, we measured the
 effects of Sativex® on clinically measured spasticity and on neurophysiological and laboratory parameters that correlate with spasticity severity
 or with the modulation of the ECS. Sativex® failed to affect spasticity and stretch reflex e...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2816888</comments>
            <pubDate>Sat, 19 Sep 2009 05:51:39 +0100</pubDate>
            <guid isPermaLink="false">2816888</guid>        </item>
        <item>
            <title>Normative data for the Pyramids and Palm Trees Test in the elderly Italian population</title>
            <link>http://www.medworm.com/index.php?rid=2816890&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fxk31745l4n7p7670%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The Pyramids and Palm Tree Test (PPT) is a semantic memory test that measures the capacity to access detailed semantic information
 about words and pictures, necessary for the identification of the analogies, which link conceptually two perceptually, and
 functionally distinct entities. The present study aimed to provide normative data on a large sample of the elderly Italian
 population (N&amp;nbsp;=&amp;nbsp;464; range of age&amp;nbsp;=&amp;nbsp;49–94; range of education&amp;nbsp;=&amp;nbsp;3–25) on both the word and the picture versions of the PPT. Results from
 multiple regression analyses showed that both age and education were significant predictors of performance in both the word
 and the picture versions of the PPT. Therefore, norms were calculated taking into account these demogra...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2816890</comments>
            <pubDate>Sat, 19 Sep 2009 05:51:38 +0100</pubDate>
            <guid isPermaLink="false">2816890</guid>        </item>
        <item>
            <title>Bilateral facial nerve enhancement demonstrated by magnetic resonance imaging in Guillain–Barre Syndrome</title>
            <link>http://www.medworm.com/index.php?rid=2745049&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F48850638548u8v6m%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Guillain–Barré syndrome (GBS) is an acute inflammatory demyelinating peripheral nerve disorder. It is known that gadolinium
 enhancement on magnetic resonance imaging (MRI) reflects alteration of the blood–nerve barrier secondary to inflammation.
 Enhancement of the cauda equina roots with gadolinium on lumbosacral magnetic resonance imaging have been demonstrated in
 several reports. Although about 50% of GBS patients clinically exhibit facial nerve involvement, it has never been demonstrated
 on MRI. We aimed to observe facial nerve involvement in a GBS patient who has prominent facial diplegia. With the guidance
 of the literature, we predict that MRI in selected GBS patients may be an adjunct tool for the clinician in both diagnosis
 and monitoring the treatmen...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2745049</comments>
            <pubDate>Fri, 28 Aug 2009 15:00:15 +0100</pubDate>
            <guid isPermaLink="false">2745049</guid>        </item>
        <item>
            <title>Bovine serum albumin promotes IL-1β and TNF-α secretion by N9 microglial cells</title>
            <link>http://www.medworm.com/index.php?rid=2723745&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff1l5464696036k13%2F</link>
            <description>In this study, we observed that BSA induced significant upregulation of
 mRNA expression and release of pro-inflammatory cytokines, IL-1β, and TNF-α, by N9 microglial cells. Our results suggest that
 the effects of BSA should be taken into account in experiments on microglia or the central nervous system when BSA is used.
 In light of the high similarity and homology among mammalian albumins, our findings also indicate that serum albumin may be
 a potent trigger of cytokine release by microglia.
 
	Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s10072-009-0123-xAuthors
		Tian-zhi Zhao, The Third Military Medical University Department of Neurosurgery, Southwest Hospital Chongqing 400038 ChinaYong-zhi Xia, The Third Military Medical University Department of Neurosurgery, ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2723745</comments>
            <pubDate>Fri, 21 Aug 2009 11:11:10 +0100</pubDate>
            <guid isPermaLink="false">2723745</guid>        </item>
        <item>
            <title>Epilepsia partialis continua in type 1 diabetes: evolution into epileptic encephalopathy with continuous spike-waves during slow sleep</title>
            <link>http://www.medworm.com/index.php?rid=2706808&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp4584064g42647t2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hyperglycemic status may be rarely complicated by Epilepsia partialis continua (EPC) that usually responds to metabolic normalization. Anti-glutamic acid decarboxylase antibodies (GAD-Ab) play a pivotal
 role in the autoimmune process that leads to clinical onset of type 1 diabetes mellitus (T1DM). GAD-Ab have been recently
 reported in association with rare forms of refractory epilepsy, with or without association to T1DM. Here we describe a young
 patient who developed EPC five months after T1DM onset; GAD-Ab were detected in his cerebrospinal fluid with evidence of oligoclonal
 bands. His epileptic disorder evolved over time into drug-resistant epilepsy with continuous spike-waves during slow sleep
 and severe behavioral impairment. The role of both metabolic imbalan...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2706808</comments>
            <pubDate>Sat, 15 Aug 2009 09:36:58 +0100</pubDate>
            <guid isPermaLink="false">2706808</guid>        </item>
        <item>
            <title>Unusual Parsonage–Turner syndrome with relapses and bilateral simultaneous anterior interosseous neuropathy</title>
            <link>http://www.medworm.com/index.php?rid=2706809&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff7l4l739048xg057%2F</link>
            <description>We report an unusual case of Parsonage–Turner syndrome with relapses and simultaneous bilateral anterior interosseous neuropathy
 (AIN). A 66-year-old man, after a typical right brachial amyotrophic neuralgia few months previously, underwent surgery for
 left carpal tunnel syndrome. The day following surgery, wrist aching and bilateral weakness, even if prevalent on the right
 side, on thumb and index finger flexion appeared. Neurophysiology was consistent with bilateral AIN neuropathy and serology
 revealed anti-nucleus antibody positivity. Association of relapses with bilateral acute AIN involvement in the subject with
 autoantibody detection can suggest an immunological pathogenesis.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0124-9Authors
		Giovanna Squ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2706809</comments>
            <pubDate>Sat, 15 Aug 2009 09:36:56 +0100</pubDate>
            <guid isPermaLink="false">2706809</guid>        </item>
        <item>
            <title>Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis</title>
            <link>http://www.medworm.com/index.php?rid=2706810&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7346x03278370620%2F</link>
            <description>We describe a patient with a sporadic form of amyotrophic lateral sclerosis (ALS) in which a heterozygous
 A&amp;nbsp;&amp;gt;&amp;nbsp;C exchange at position 272 in the SOD1 gene was detected. This mutation results in an amino acid substitution of alanine for aspartate at position 90 (D90A). The
 patient had a 12-year history of disease characterized by slow progression. Clinical examination at last follow-up revealed
 predominant upper motor neuron (p-UMN) involvement, with atrophies only in distal muscle of upper limbs. Electrophysiological
 examination revealed lower and upper motor neuron involvement. Family history was negative for neurological disease. This
 report shows that D90A in heterozygous state may cause p-UMN phenotype with very slow progression.
 
	Content Type Journal ArticleCategory...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2706810</comments>
            <pubDate>Sat, 15 Aug 2009 09:36:51 +0100</pubDate>
            <guid isPermaLink="false">2706810</guid>        </item>
        <item>
            <title>Neurofunctional assessment in a case of calculation-induced seizures</title>
            <link>http://www.medworm.com/index.php?rid=2706811&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx5w57qw91n5l2847%2F</link>
            <description>We report
 the case of patient affected by calculation-induced seizures that were refractory to medications. We showed the cortical activation
 by using a functional magnetic resonance imaging (fMRI) while he was performing an arithmetic task and illustrated that, in
 this case, the areas commonly activated included the premotor and supplementary motor areas of both hemispheres. Furthermore,
 the patient showed a more significant activation of posterior parietal and prefrontal cortices after arithmetic tasks if compared
 to normal controls. To our knowledge, this is the first fMRI study in calculation-induced seizures, even if limited to a single
 patient. The potential benefits of non-conventional neuroimaging technology, such as fMRI, for understanding calculation,
 however, are only beg...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2706811</comments>
            <pubDate>Sat, 15 Aug 2009 09:36:44 +0100</pubDate>
            <guid isPermaLink="false">2706811</guid>        </item>
        <item>
            <title>Regression of chronic posterior leukoencephalopathy after stop of methotrexate treatment</title>
            <link>http://www.medworm.com/index.php?rid=2643166&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp4380l2711896514%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Posterior reversible leukoencephalopathy (PRLE) is a neurological disorder caused by a variety of pathological conditions
 such as high doses or long-term low-doses of immunosuppressive therapy. PRLE associated with methotrexate (MTX) is well known
 but it was rarely observed in adult patients submitted to long-term low-dose administration via the oral route. Here we report
 the case of a patient affected by psoriasis, treated by chronic oral low-dose of MTX, who presented with limb ideomotor apraxia.
 Magnetic resonance (MRI) of the brain showed, on T2-weighted images, a diffuse hyperintensity involving bilaterally the white
 matter of the occipital, parietal and frontal lobes. MTX treatment was stopped and, at the 6-month follow-up, the neuropsychological
 performance...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2643166</comments>
            <pubDate>Fri, 24 Jul 2009 23:51:11 +0100</pubDate>
            <guid isPermaLink="false">2643166</guid>        </item>
        <item>
            <title>Schilder’s disease: non-invasive diagnosis?</title>
            <link>http://www.medworm.com/index.php?rid=2623740&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fgw67v4wk8g648847%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Schilder’s disease, or myelinoclastic diffuse sclerosis, is a rare disorder characterised by an inflammatory white matter
 plaque of demyelination. Clinical signs and symptoms might be atypical for early multiple sclerosis and at imaging the lesion
 is easily taken for a brain tumour. Regardless of the use of Poser’s criteria for clinical diagnosis of Schilder’s disease
 proposed in 1986, diagnostic difficulties are still present, as evidenced by the many reported cases in the English literature
 revised (Pubmed indexed, period 1998–2008). It clearly emerges that neuroradiological features, observable in additional magnetic
 resonance sequences are crucial, besides the consideration of Poser’s criteria, in differentiating between demyelinating lesions
 and bra...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2623740</comments>
            <pubDate>Sat, 18 Jul 2009 21:13:05 +0100</pubDate>
            <guid isPermaLink="false">2623740</guid>        </item>
        <item>
            <title>Creutzfeldt–Jakob disease with E200K PRNP mutation: a case report and revision of the literature</title>
            <link>http://www.medworm.com/index.php?rid=2604150&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn67p550w76653q83%2F</link>
            <description>We report a 63-year-old Italian woman harboring the E200K PRNP mutation. Electroencephalogram, cerebrospinal fluid analysis, PRNP gene sequencing, histopathologic examination, immunohistochemical studies, and Western blotting analysis confirmed the diagnosis
 of CJD. Pyramidal involvement was the first sign and the prominent clinical feature. Later on, she developed also myoclonus,
 ataxia, spastic tetraplegia, and at last dementia with akinetic mutism. Usually, signs of degeneration of the pyramidal tracts
 occur in a small number of patients as the disease advances. Our report supports the variability of the clinical expression
 of the E200K genetic CJD. Further studies are needed to understand the molecular basis underlying the phenotypic variability
 among patients carrying this mutati...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2604150</comments>
            <pubDate>Tue, 14 Jul 2009 10:03:06 +0100</pubDate>
            <guid isPermaLink="false">2604150</guid>        </item>
        <item>
            <title>Neuropsychiatric symptoms and the APOE genotype in Alzheimer’s disease</title>
            <link>http://www.medworm.com/index.php?rid=2592440&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc7655730m1253320%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The study aimed to characterize neuropsychiatric symptomatology in Alzheimer’s disease (AD) and investigate the role of APOE
 genotype and other clinical variables in the onset of neuropsychiatric disorders. Moreover, an attempt to study the evolution
 of behavioral and psychiatric symptoms was made. Fifty-three consecutive outpatients with AD were enrolled. Twenty-four were
 followed longitudinally for 1&amp;nbsp;year. MMSE was used to evaluate cognitive functions. The neuropsychiatric inventory (NPI) was
 administered to assess behavioral and psychiatric symptoms. Genotyping was determined through laboratory testing. At baseline,
 no specific neuropsychiatric disorder was significantly associated with ApoE genotype, but associated with a peculiar neuropsychiatric
 profi...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2592440</comments>
            <pubDate>Fri, 10 Jul 2009 08:14:48 +0100</pubDate>
            <guid isPermaLink="false">2592440</guid>        </item>
        <item>
            <title>Selective involvement of temporal regions in a case of flavivirus encephalitis</title>
            <link>http://www.medworm.com/index.php?rid=2592439&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc2665044133103n2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Clinical manifestations of flavivirus infection may be various, from unapparent to severe meningoencephalitis. Our patient,
 2&amp;nbsp;weeks after returning home from a holiday at Elba Island, developed biphasic fever, later associated with nausea and vomiting
 and followed by incoming seizures responsive to thiopental sodium only. Brain MRI showed bilateral hyperintensity (T2) in
 amygdale, hippocampus, left insular and temporal inferior cortex. Standard and microbiological CSF examination was normal,
 but microbiological serum analysis showed seroconversion for flavivirus. The patient came to our observation 6&amp;nbsp;months after
 disease onset and at that time he was affected by frequent seizures and severe cognitive impairment with behavioural disturbances;
 the patient ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2592439</comments>
            <pubDate>Fri, 10 Jul 2009 08:14:48 +0100</pubDate>
            <guid isPermaLink="false">2592439</guid>        </item>
        <item>
            <title>Stereoanesthesia or astereognosia?</title>
            <link>http://www.medworm.com/index.php?rid=2592441&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk421227860154276%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;This case attempts to explicit the importance of clinical examination in the differential diagnosis of two similar clinical
 entities namely astereognosia and stereoanesthesia. The patient presented below involves a multiple sclerosis patient whose
 symptoms were considered at first to be a case of astereognosia since she mainly complained of an inability to recognize and
 name the form and nature of objects by touch. However, a thorough clinical examination and the results of neurophysiological
 and neuroimaging testing demonstrated that it involved a case of stereoanesthesia due to a demyelinating lesion at the cervical
 region of the spinal cord.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0117-8Authors
		E. Kararizou, Athens National Un...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2592441</comments>
            <pubDate>Thu, 09 Jul 2009 12:11:22 +0100</pubDate>
            <guid isPermaLink="false">2592441</guid>        </item>
        <item>
            <title>Restless legs syndrome in a patient with multifocal motor neuropathy</title>
            <link>http://www.medworm.com/index.php?rid=2578630&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft2421mu807h31237%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Restless legs syndrome (RLS) has been frequently reported in association with peripheral neuropathy, and it is especially
 frequent in some forms of polyneuropathy with preferential involvement of small sensory fibers. Here, we describe a patient
 with multifocal motor neuropathy, who developed RLS during the course of the disease. Our findings support the notion that
 RLS may develop in the context of immune-mediated neuropathies and it should be specifically investigated even in those patients
 with preferentially or exclusive motor involvement.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0111-1Authors
		Daniele Lo Coco, Ospedale Civico, ARNAS U.O. Neurologia, Dipartimento di Neuroscienze P.za N. Leotta 4 90129 Palermo ItalyEmanuele Canni...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2578630</comments>
            <pubDate>Mon, 06 Jul 2009 17:07:54 +0100</pubDate>
            <guid isPermaLink="false">2578630</guid>        </item>
        <item>
            <title>Aseptic meningitis as the sole manifestation of Behçet’s disease</title>
            <link>http://www.medworm.com/index.php?rid=2578631&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F24781q2101434257%2F</link>
            <description>We report a 33-year-old woman who had aseptic meningitis alone, without any other systemic manifestations, due to Behçet’s
 disease. Behçet’s disease should be listed as a differential diagnosis of acute aseptic meningitis because, in acute aseptic
 meningitis caused by Behçet’s disease, early treatment with corticosteroids could ameliorate this disorder.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0109-8Authors
		Ryuji Sakakibara, Sakura Medical Center, Toho University Neurology Division, Department of Internal Medicine 564-1 Shimoshizu Sakura 285-8741 JapanNobukiyo Koide, Sakura Medical Center, Toho University Endocrinology and Metabolism Division, Department of Internal Medicine Sakura JapanMasahiko Kishi, Sakura Medical Center, Toho University Neu...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2578631</comments>
            <pubDate>Mon, 06 Jul 2009 17:07:53 +0100</pubDate>
            <guid isPermaLink="false">2578631</guid>        </item>
        <item>
            <title>S-adenosylmethionine and S-adenosylhomocysteine levels in the aging brain of APP/PS1 Alzheimer mice</title>
            <link>http://www.medworm.com/index.php?rid=2565594&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx5h7j42700158422%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hyperhomocysteinemia and factors of homocysteine metabolism, S-adenosylhomocysteine (AdoHcy) and S-adenosylmethionine (AdoMet), may play a role in Alzheimer’s disease (AD). With liquid-chromatography-tandem-mass-spectrometry
 AdoMet and AdoHcy were determined in brains of 8- and 15-month-old APP/PS1 Alzheimer mice, and their possible roles in AD
 brains investigated. The finding that AdoMet levels do not differ between the genotypes in (young) 8-month-old mice, but are
 different in (older) 15-month-old APP/PS1 mice compared to their wild-type littermates, suggests that alterations in AdoMet
 are a consequence of AD pathology rather than a cause. During aging, AdoMet levels decreased in the brains of wild-type mice,
 whereas AdoHcy levels diminished in both wild type ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2565594</comments>
            <pubDate>Tue, 30 Jun 2009 15:44:29 +0100</pubDate>
            <guid isPermaLink="false">2565594</guid>        </item>
        <item>
            <title>A possible paraneoplastic neuromyelitis optica associated with lung cancer</title>
            <link>http://www.medworm.com/index.php?rid=2565595&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fjq8504287k8x8246%2F</link>
            <description>We describe here a 63-year-old
 woman who presented to our local hospital with an acute, bilateral visual loss followed by progressive paraparesis. Medical
 evaluations revealed a lung tumor and spinal MRI showed multiple cervical-dorsal hyperintense T2 lesions with mild mass effect. Testing for NMO-Ig resulted positive. Patient’s diagnosis was thus consistent with a possible
 paraneoplastic neuromyelitis optica associated with non-small cell lung cancer and evidence of NMO-Ig.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0112-0Authors
		Giuseppe De Santis, Institute of Clinical Neurology Department of Medical-Surgical Disciplines, Communication and Behaviour Corso Giovecca, 203 44100 Ferrara ItalyLuisa Caniatti, Institute of Clinical Neurology Department of ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2565595</comments>
            <pubDate>Tue, 30 Jun 2009 15:44:19 +0100</pubDate>
            <guid isPermaLink="false">2565595</guid>        </item>
        <item>
            <title>Intracranial and intraspinal hemorrhage following spinal anesthesia</title>
            <link>http://www.medworm.com/index.php?rid=2565596&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F283q61015t6j4j18%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Spinal anesthesia (SA), accounting for more than 50% of regional anesthesias in the spinal region, is generally perceived
 as simple and safe. Our purpose is to increase awareness of hemorrhagic complications following SA. A 69-year-old male without
 either coagulation disorders or anticoagulant/antiplatelet therapy developed acute radiculopathy, and severe mental confusion
 after SA for prostatectomy. CT showed intracranial subarachnoid and intraventricular acute hemorrhage. Cerebral angiography
 was negative. MRI showed subarachnoid and subdural hematoma in the dorsolumbar spine. Seven-year follow-up showed permanent
 cognitive and radicular damage. Multiple attempts for SA most likely caused spinal vessels rupture, either directly or indirectly
 by inducing different...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2565596</comments>
            <pubDate>Tue, 30 Jun 2009 15:44:18 +0100</pubDate>
            <guid isPermaLink="false">2565596</guid>        </item>
        <item>
            <title>Central sleep apnoea in Rett syndrome</title>
            <link>http://www.medworm.com/index.php?rid=2549694&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr754481p7p745316%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Breathing disturbances in Rett syndrome were reported almost entirely during wakefulness, with normal respiration during sleep.
 We studied a case of a proven MECP2 mutation in a girl, whose videopolygraphic and polysomnographic monitoring suggested the
 evidence of central apnoeas not only during awake, but also during sleep. Apart from prevalent awake respiratory dysfunction,
 central apnoeas in Rett syndrome may be also present during sleep.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0108-9Authors
		Giuseppe d’Orsi, Opera Don Uva Epilepsy Center, Neurological Unit, Casa Divina Provvidenza Via Bovio 78 70052 Bisceglie (BAT) ItalyVincenzo Demaio, Opera Don Uva Epilepsy Center, Neurological Unit, Casa Divina Provvidenza Via Bovio 78 7005...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2549694</comments>
            <pubDate>Thu, 25 Jun 2009 07:39:24 +0100</pubDate>
            <guid isPermaLink="false">2549694</guid>        </item>
        <item>
            <title>Orthostatic tremor and I123-FP-CIT-SPECT: report of a case</title>
            <link>http://www.medworm.com/index.php?rid=2492154&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy71x31770m045r11%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorDOI 10.1007/s10072-009-0105-zAuthors
		Francesco Raudino, “Valduce” Hospital Department of Neurology Via Dante 11 22100 Como ItalyFrancesco Muscia, “Valduce” Hospital Department of Neurology Via Dante 11 22100 Como ItalyMaurizio Osio, “L. Sacco” Hospital Department of Neurology Milan Italy
	

	
		Journal Neurological SciencesOnline ISSN 1590-3478Print ISSN 1590-1874 (Source: Neurological Sciences)</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2492154</comments>
            <pubDate>Wed, 17 Jun 2009 09:43:17 +0100</pubDate>
            <guid isPermaLink="false">2492154</guid>        </item>
        <item>
            <title>Clinical features of psychogenic non-epileptic seizures in prepubertal and pubertal patients with idiopathic epilepsy</title>
            <link>http://www.medworm.com/index.php?rid=2492153&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F010713667g68552n%2F</link>
            <description>In this study, we reviewed
 36 patients from six neurological referral centres: Department of Pediatrics, Chieti (3 patients); Department of Child Neuropsychiatry,
 Naples (9 patients); Department of Child Neuropsychiatry, Bologna (8 patients); Department of Neuroscience, Tor Vergata University,
 Rome (3 patients); Department of Pediatrics, La Sapienza University, Rome (5 patients); and Department of Pediatrics, Siena
 (8 patients). The population was divided according to Tanner’stages into 14 prepubertal (group I) and 22 pubertal (group II)
 patients. The two groups were compared on several variables examining the differences between them. The most frequent clinical
 manifestations in group I were unresponsive events, whereas in group II, motor events were exhibited more significantly. ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2492153</comments>
            <pubDate>Wed, 17 Jun 2009 09:43:17 +0100</pubDate>
            <guid isPermaLink="false">2492153</guid>        </item>
        <item>
            <title>Myasthenia gravis initially presenting with pseudo-internuclear ophthalmoplegia</title>
            <link>http://www.medworm.com/index.php?rid=2492152&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fgu5052507333531v%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Myasthenia gravis (MG) can rarely be manifested with ocular motility disturbances, simulating internuclear ophthalmoplegia.
 Pseudo-internuclear ophthalmoplegia (PINO) may occur during the course of MG, however, the initial presentation of MG with
 PINO in rather unlikely. We herein describe the case of a male patient who developed PINO, as an initial manifestation of
 MG.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0106-yAuthors
		Andreas A. Argyriou, “Saint Andrew’s” General Hospital of Patras Department of Neurology 26335 Patras GreecePanagiotis Karanasios, “Saint Andrew’s” General Hospital of Patras Department of Neurology 26335 Patras GreeceCharalabos Potsios, “Saint Andrew’s” General Hospital of Patras Department of ...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2492152</comments>
            <pubDate>Wed, 17 Jun 2009 09:43:17 +0100</pubDate>
            <guid isPermaLink="false">2492152</guid>        </item>
        <item>
            <title>Multifocal myoclonus induced by haloperidol</title>
            <link>http://www.medworm.com/index.php?rid=2480503&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0h7u807j3713306m%2F</link>
            <description>We report
 the first case of a patient with severe Alzheimer’s disease who presented with non-epileptic myoclonus just after haloperidol
 treatment was initiated.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0104-0Authors
		Cristina Domínguez, University Hospital “12 de Octubre” Department of Neurology Madrid SpainJulián Benito-León, University Hospital “12 de Octubre” Department of Neurology Madrid SpainFélix Bermejo-Pareja, University Hospital “12 de Octubre” Department of Neurology Madrid Spain
	

	
		Journal Neurological SciencesOnline ISSN 1590-3478Print ISSN 1590-1874 (Source: Neurological Sciences)</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2480503</comments>
            <pubDate>Sat, 13 Jun 2009 08:23:08 +0100</pubDate>
            <guid isPermaLink="false">2480503</guid>        </item>
        <item>
            <title>Preliminary evaluation of the DDS-PC inventory: a new tool to assess impulsive–compulsive behaviours associated to dopamine replacement therapy in Parkinson’s disease</title>
            <link>http://www.medworm.com/index.php?rid=2480504&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F268rh0p026x703q8%2F</link>
            <description>We report a preliminary evaluation of a questionnaire to assess the presence of these impulsive–compulsive
 behaviours associated to dopamine replacement therapy in PD. We screened 38 patients and their caregivers, comparing dopamine
 dysregulation syndrome (DDS) patients and non-DDS patients. The questionnaire was well accepted and demonstrated a preliminary
 good discriminant validity (p&amp;nbsp;=&amp;nbsp;0.000). In addition, clinically relevant dysregulated condition is associated with a younger age (p&amp;nbsp;=&amp;nbsp;0.006), younger age at disease onset (p&amp;nbsp;=&amp;nbsp;0.001), levodopa-equivalent daily dose (p&amp;nbsp;=&amp;nbsp;0.029), UPDRS III (p&amp;nbsp;=&amp;nbsp;0.021), increased global psychopathology (interpersonal sensitivity and psychoticism), and differences in our inventory
 (p&amp;nbsp;=&amp;nbsp;0.000)...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2480504</comments>
            <pubDate>Wed, 10 Jun 2009 09:54:11 +0100</pubDate>
            <guid isPermaLink="false">2480504</guid>        </item>
        <item>
            <title>Death in Unverricht–Lundborg disease</title>
            <link>http://www.medworm.com/index.php?rid=2460833&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy07t5477112u2g90%2F</link>
            <description>In conclusion, although the prognosis of ULD has progressed, there are still spontaneously severe forms and
 high risk of early death, including SUDEP.
 
	Content Type Journal ArticleCategory Original ArticleDOI 10.1007/s10072-009-0102-2Authors
		Hela Mrabet Khiari, Charles Nicolle Hospital Neurological Department Boulevard 9 Avril 1006 Tunis TunisiaSilvana Franceschetti, Besta Neurological Institute Department of Neurology Milan ItalyNebojsa Jovic, Clinic of Neurology and Psychiatry for Children and Youth Belgrade SerbiaAmel Mrabet, Charles Nicolle Hospital Neurological Department Boulevard 9 Avril 1006 Tunis TunisiaPierre Genton, Centre Saint Paul-Henri Gastaut Marseille France
	

	
		Journal Neurological SciencesOnline ISSN 1590-3478Print ISSN 1590-1874 (Source: Neurological Sciences)</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2460833</comments>
            <pubDate>Fri, 05 Jun 2009 08:57:09 +0100</pubDate>
            <guid isPermaLink="false">2460833</guid>        </item>
        <item>
            <title>Use of a single [123I]-FP-CIT SPECT to predict the severity of clinical symptoms of Parkinson disease</title>
            <link>http://www.medworm.com/index.php?rid=2460834&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F785357730m8114g7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of this study was to assess the ability of a single SPECT performed in the early stage of Parkinson’s disease (PD)
 to predict disease severity in 19 patients with early PD. [123I]-FP-CIT striatal uptake was expressed as a ratio of specific:nonspecific uptake for defined brain areas. Clinical severity
 was determined by the UPDRS at baseline and 12–15&amp;nbsp;months following the SPECT procedure. [123I]-FP-CIT uptake in the contralateral putamen and striatum was correlated with UPDRS score at baseline, with a more significant
 correlation after 1-year interval. [123I]-FP-CIT uptake in all areas was correlated with bradykinesia and rigidity subscores only at follow up visit. Significant
 correlations were found between [123I]-FP-CIT uptake in the contralateral s...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2460834</comments>
            <pubDate>Fri, 05 Jun 2009 08:57:08 +0100</pubDate>
            <guid isPermaLink="false">2460834</guid>        </item>
        <item>
            <title>Medulla oblongata tuberculoma mimicking metastasis presenting with stroke-like symptoms</title>
            <link>http://www.medworm.com/index.php?rid=2460835&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm716835ukrvw7172%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Tuberculomas are common forms of central nervous system tuberculosis, presenting as space-occupying-lesions. Brainstem tuberculomas
 are rare among all intracranial tuberculomas. In old patients, in the absence of tuberculosis history, diagnosis may be challenging.
 In this case, we present a 70-year-old patient, with bladder cancer, without known tuberculosis who presented with stroke-like
 symptoms, clinically. Diffusion-weighted imaging revealed no finding of stroke, however, a medulla oblongata tuberculoma,
 mimicking metastasis was evident on MRI.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s10072-009-0099-6Authors
		Fuldem Yildirim Donmez, Baskent University Faculty of Medicine Department of Radiology 46. Sokak No: 11/8, Bahcelievler Ankara Turk...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2460835</comments>
            <pubDate>Thu, 04 Jun 2009 11:17:17 +0100</pubDate>
            <guid isPermaLink="false">2460835</guid>        </item>
        <item>
            <title>ID migraine questionnaire in temporomandibular disorders with craniofacial pain: a study by using a multidisciplinary approach</title>
            <link>http://www.medworm.com/index.php?rid=2460836&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F57273717r8l73642%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To evaluate the prevalence of migraine and related disability and the role of ID migraine questionnaire as a screening tool
 in patients with temporomandibular disorders (TMDs) and craniofacial pain (CFP). TMDs patients with CFP underwent stomatognathic
 (RDC/TMD criteria) and neurological visits (IHS criteria, 2004). ID migraine questionnaire and MIgraine Disability Assessment
 Scale (MIDAS) were also administered. Out of 45 patients, 69% met diagnosis of migraine plus chronic tension-type headache
 (CTTH); 9% presented CTTH and 20% were migraineurs. Out of 39 migraineurs who completed MIDAS, 56% presented the highest disability
 grade. Out of 37 patients who completed ID migraine questionnaire, 32 resulted affected by probable migraine with a diagnostic
 sensibility a...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2460836</comments>
            <pubDate>Thu, 04 Jun 2009 11:17:16 +0100</pubDate>
            <guid isPermaLink="false">2460836</guid>        </item>
        <item>
            <title>Blood levels of homocysteine, cysteine, glutathione, folic acid, and vitamin B12 in the acute phase of atherothrombotic stroke</title>
            <link>http://www.medworm.com/index.php?rid=2450382&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7104l69523452318%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Blood levels of total homocysteine (tHcy), cysteine (Cys), total and reduced glutathione (tGSH and rGSH), folic acid (FA),
 and vitamin B12 (B12) change during ischemic stroke as accompaniment of the tissue damage. The relationship between these changes remains scantly
 investigated. We evaluated the variation of these molecules in the 48&amp;nbsp;h after acute large artery atherothrombotic stroke (LAAS)
 and searched for the presence of matched variation of them. The study involved 50 subjects affected by acute LAAS and 49 healthy
 controls. Plasma levels of tHcy and Cys were significantly higher and serum levels of FA and B12 and plasma levels of rGSH were significantly lower in the patients than in the control group. Acute LAAS was associated with
 increased Hcy—decrea...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2450382</comments>
            <pubDate>Sat, 30 May 2009 07:46:20 +0100</pubDate>
            <guid isPermaLink="false">2450382</guid>        </item>
        <item>
            <title>Simultaneous measurement of 23 plasma cytokines in late-life depression</title>
            <link>http://www.medworm.com/index.php?rid=2450383&amp;cid=s_33319_25_f&amp;fid=33319&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx414055p8161060t%2F</link>
            <description>In this study, we used a bioplex assay to simultaneously measure the levels of 23 plasma cytokines
 in 18 patients with late-life depression and 38 normal controls, and these levels were compared between the two groups. The
 plasma interleukin-1alpha (IL-1α) levels were found to be significantly different between the two groups. After adjusting
 for age, gender, low-density lipoprotein cholesterol, and triglyceride, the plasma IL-1α levels were significantly higher
 in the patients with late-life depression than in the normal control subjects. Thus, this study provides preliminary evidence
 that plasma IL-1α may play important roles in the pathogenesis of late-life depression.
 
	Content Type Journal ArticleCategory Brief CommunicationDOI 10.1007/s10072-009-0091-1Authors
		Kang Soo Lee,...</description>
            <author>Neurological Sciences</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2450383</comments>
            <pubDate>Sat, 30 May 2009 07:46:19 +0100</pubDate>
            <guid isPermaLink="false">2450383</guid>        </item>
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