<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0">
    <channel>
        <title>Journal of Neurology 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 'Journal of Neurology' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Journal+of+Neurology&t=Journal+of+Neurology&s=Search&f=source]]></link>
        <lastBuildDate>Wed, 08 Feb 2012 20:43:16 +0100</lastBuildDate>
        <item>
            <title>Analysis of myelinated fibers in human skin biopsies of patients with neuropathies</title>
            <link>http://www.medworm.com/index.php?rid=5668697&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F93514242104r358m%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Given the availability of effective but costly treatment for acquired demyelinating neuropathies, biomarkers for these disorders
 are urgently needed. Here we aimed to quantify morphological abnormalities of myelinated fibers in skin biopsies from the
 proximal leg of patients with neuropathies to determine a potential diagnostic role of this method. We used double immunofluorescence
 to detect myelinated and unmyelinated fibers in thigh skin from 81 patients with polyneuropathy, 19 patients with small fiber
 neuropathy, and 25 controls. Dermal myelinated fibers were reduced 6.8-fold in patients with polyneuropathy (p&amp;nbsp;&amp;lt;&amp;nbsp;0.0001). The number of dermal nerve bundles with myelinated fibers was reduced 2.7-fold (p&amp;nbsp;=&amp;nbsp;0.0025). In small fiber neuropathy, ...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5668697</comments>
            <pubDate>Mon, 06 Feb 2012 19:36:54 +0100</pubDate>
            <guid isPermaLink="false">5668697</guid>        </item>
        <item>
            <title>Diagnostic pitfalls: a case of neurosarcoidosis mimicking tuberculous meningitis</title>
            <link>http://www.medworm.com/index.php?rid=5660881&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft573lw777167k707%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-4DOI 10.1007/s00415-012-6429-2Authors
		Franziska Scheibe, Department of Neurology, Charité–Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, GermanyHolger Flick, UKIM-LKH Universitätsklinikum/Medizinische Universität Graz, Auenbruggerplatz 20, 8036 Graz, AustriaOliver Wengert, Department of Neurology, Charité–Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, GermanyDaniel Wittschieber, Department of Pathology, Charité–Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, GermanyGeorg Bohner, Department of Radiology, Charité–Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, GermanyPeter Ruokonen, Department of Ophthalmology, Charité–Universitätsmedizin Berlin, Augustenb...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660881</comments>
            <pubDate>Fri, 03 Feb 2012 17:12:04 +0100</pubDate>
            <guid isPermaLink="false">5660881</guid>        </item>
        <item>
            <title>Quantitative assessment of visual behavior in disorders of consciousness</title>
            <link>http://www.medworm.com/index.php?rid=5660882&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F857m8163l6278872%2F</link>
            <description>In this study we aimed to provide a quantitative assessment of visual tracking behavior
 in response to moving stimuli in DoC patients. Nine VS patients and nine MCS patients were recruited in a Neurorehabilitation
 Unit for patients with chronic DoC; 11 matched healthy subjects were tested as the control group. All participants underwent
 a quantitative evaluation of eye-tracking pattern by means of a computerized infrared eye-tracker system; stimuli were represented
 by a red circle or a small color picture slowly moving on a PC monitor. The proportion of on- or off-target fixations differed
 significantly between MCS and VS. Most importantly, the distribution of fixations on or off the target in all VS patients
 was at or below the chance level, whereas in the MCS group seven out of nin...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660882</comments>
            <pubDate>Fri, 03 Feb 2012 07:20:39 +0100</pubDate>
            <guid isPermaLink="false">5660882</guid>        </item>
        <item>
            <title>Rhazes (865–925 AD)</title>
            <link>http://www.medworm.com/index.php?rid=5660884&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fqp033v453507k2qp%2F</link>
            <description>Content Type Journal ArticleCategory Pioneers in NeurologyPages 1-2DOI 10.1007/s00415-011-6398-xAuthors
		Mohamad M. Zarshenas, Research Office for the History of Persian Medicine, Shiraz University of Medical Sciences, Shiraz, IranAlireza Mehdizadeh, Research Office for the History of Persian Medicine, Shiraz University of Medical Sciences, Shiraz, IranArman Zargaran, Research Office for the History of Persian Medicine, Shiraz University of Medical Sciences, Shiraz, IranAbdolali Mohagheghzadeh, Research Office for the History of Persian Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660884</comments>
            <pubDate>Thu, 02 Feb 2012 18:12:30 +0100</pubDate>
            <guid isPermaLink="false">5660884</guid>        </item>
        <item>
            <title>Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort</title>
            <link>http://www.medworm.com/index.php?rid=5660883&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F11p740m751586u22%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The hereditary sensory and autonomic neuropathies (HSAN, also known as the hereditary sensory neuropathies) are a clinically
 and genetically heterogeneous group of disorders, characterised by a progressive sensory neuropathy often complicated by ulcers
 and amputations, with variable motor and autonomic involvement. To date, mutations in twelve genes have been identified as
 causing HSAN. To study the frequency of mutations in these genes and the associated phenotypes, we screened 140 index patients
 in our inherited neuropathy cohort with a clinical diagnosis of HSAN for mutations in the coding regions of SPTLC1, RAB7, WNK1/HSN2, FAM134B, NTRK1 (TRKA) and NGFB. We identified 25 index patients with mutations in six genes associated with HSAN (SPTLC1, RAB7, WNK1/HSN2, F...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660883</comments>
            <pubDate>Thu, 02 Feb 2012 18:12:30 +0100</pubDate>
            <guid isPermaLink="false">5660883</guid>        </item>
        <item>
            <title>Migraine with aura in patients over 50 years of age: the Marseille’s registry</title>
            <link>http://www.medworm.com/index.php?rid=5660885&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0v310u340w0p028r%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The goal of this study was to describe specifically the clinical characteristics of migraine with aura in patients over the
 age of 50. During 1&amp;nbsp;year, three neurologists working in a tertiary headache center included all patients aged 50&amp;nbsp;years and
 over presenting migraine with aura in a prospective registry. Fifty-seven patients with migraine with aura aged 50&amp;nbsp;years and
 over were interviewed using a standardized questionnaire during a consultation. Auras were visual for all the patients, paresthesic
 for 16 patients, and aphasic for 16. One patient had a sporadic hemiplegic migraine. The headache followed the aura in a large
 majority of patients and fulfilled the International Headache Society criteria for migraine headache for 38 patients. Typical
 au...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660885</comments>
            <pubDate>Thu, 02 Feb 2012 18:12:29 +0100</pubDate>
            <guid isPermaLink="false">5660885</guid>        </item>
        <item>
            <title>Sir Ludwig Guttmann (1899–1980)</title>
            <link>http://www.medworm.com/index.php?rid=5660886&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl5010h30r413pu84%2F</link>
            <description>Content Type Journal ArticleCategory Pioneers in NeurologyPages 1-3DOI 10.1007/s00415-012-6431-8Authors
		Frank W. Stahnisch, Department of Community Health Sciences, Hotchkiss Brain Institute, Institute for Public Health, University of Calgary, 3280 Hospital Drive N.W., Calgary, AB T2N 4Z6, CanadaJeremy D. Tynedal, Department of Community Health Sciences, Hotchkiss Brain Institute, Institute for Public Health, University of Calgary, 3280 Hospital Drive N.W., Calgary, AB T2N 4Z6, Canada
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660886</comments>
            <pubDate>Thu, 02 Feb 2012 06:54:09 +0100</pubDate>
            <guid isPermaLink="false">5660886</guid>        </item>
        <item>
            <title>Quantitative MRI can detect subclinical disease progression in muscular dystrophy</title>
            <link>http://www.medworm.com/index.php?rid=5660890&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr40071p401u38771%2F</link>
            <description>We examined 8&amp;nbsp;patients with genetically confirmed OPMD and 5&amp;nbsp;healthy volunteers
 twice at an interval of 13&amp;nbsp;months. Motor function measurements (MFM) were assessed. Imaging at 1.5&amp;nbsp;T (Siemens Magnetom Avanto)
 comprised two axial slice groups at the largest diameter of thigh and calf and included T1w TSE, 2-point Dixon for muscular
 fat fraction (MFF) and a multi-contrast TSE sequence to calculate quantitative T2 values. T1 images were analyzed using Fischer’s
 semiquantitative 5-point (0–4) scale. MFM and visual scores showed no significant difference over the study period. Overall
 T2 values increased in patients over the study period from 49.4 to 51.6&amp;nbsp;ms, MFF increased from 19.2 to 20.7%. Neither T2 values
 nor MFF increased in controls. Changes in T2 correla...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660890</comments>
            <pubDate>Thu, 02 Feb 2012 06:54:08 +0100</pubDate>
            <guid isPermaLink="false">5660890</guid>        </item>
        <item>
            <title>Neurological deficits in a patient with selenium deficiency due to long-term total parenteral nutrition</title>
            <link>http://www.medworm.com/index.php?rid=5660889&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fjh5231k4x7562885%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-012-6427-4Authors
		Takuya Oguri, Department of Neurology and Neuroscience, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-ku, Nagoya, 467-8601 JapanManabu Hattori, Department of Neurology and Neuroscience, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-ku, Nagoya, 467-8601 JapanTakemori Yamawaki, Department of Neurology and Neuroscience, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-ku, Nagoya, 467-8601 JapanSatoshi Tanida, Department of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-ku, Nagoya, 467-8601 JapanMakoto Sasaki, Department of Gastr...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660889</comments>
            <pubDate>Thu, 02 Feb 2012 06:54:08 +0100</pubDate>
            <guid isPermaLink="false">5660889</guid>        </item>
        <item>
            <title>Alfred Fuchs (1870–1927)</title>
            <link>http://www.medworm.com/index.php?rid=5660888&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ftv127vu725145136%2F</link>
            <description>Content Type Journal ArticleCategory Pioneers in NeurologyPages 1-2DOI 10.1007/s00415-012-6433-6Authors
		Lazaros C. Triarhou, Economo-Koskinas Wing for Integrative and Evolutionary Neuroscience, University of Macedonia, Thessaloniki, Greece
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660888</comments>
            <pubDate>Thu, 02 Feb 2012 06:54:08 +0100</pubDate>
            <guid isPermaLink="false">5660888</guid>        </item>
        <item>
            <title>Genetic screening of Greek patients with Huntington's disease phenocopies identifies an SCA8 expansion</title>
            <link>http://www.medworm.com/index.php?rid=5660887&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbt5h581271r55601%2F</link>
            <description>In this study we screened a cohort of 21 Greek patients with
 HD phenocopy syndromes for mutations causing HDL2, SCA17, SCA1, SCA2, SCA3, SCA8, SCA12 and DRPLA. Fifteen patients (71%)
 had a positive family history. We identified one patient (4.8% of the total cohort) with an expansion of 81 combined CTA/CTG
 repeats at the SCA8 locus. This falls within what is believed to be the high-penetrance allele range. In addition to the classic
 HD triad, the patient had features of dystonia and oculomotor apraxia. There were no cases of HDL2, SCA17, SCA1, SCA2, SCA3,
 SCA12 or DRPLA. Given the controversy surrounding the SCA8 expansion, the present finding may be incidental. However, if pathogenic,
 it broadens the phenotype that may be associated with SCA8 expansions. The absence of any other mut...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660887</comments>
            <pubDate>Thu, 02 Feb 2012 06:54:08 +0100</pubDate>
            <guid isPermaLink="false">5660887</guid>        </item>
        <item>
            <title>Assessment of dual tasking has no clinical value for fall prediction in Parkinson’s disease</title>
            <link>http://www.medworm.com/index.php?rid=5660891&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd8611417l8631182%2F</link>
            <description>The objective of this study is to investigate the value of dual-task performance for the prediction of falls in patients with
 Parkinson’s disease (PD). Two hundred sixty-three patients with PD (H&amp;Y 1–3, 65.2&amp;nbsp;±&amp;nbsp;7.9&amp;nbsp;years) walked two times along a 10-m
 trajectory, both under single-task and dual-task (DT) conditions (combined with an auditory Stroop task). To control for a
 cueing effect, Stroop stimuli were presented at variable or fixed 1- or 2-s intervals. The auditory Stroop task was also performed
 alone. Dual-task costs were calculated for gait speed, stride length, stride time, stride time variability, step and stride
 regularity, step symmetry and Stroop composite scores (accuracy/reaction time). Subsequently, falls were registered prospectively
 for 1&amp;nbsp;year...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660891</comments>
            <pubDate>Wed, 01 Feb 2012 18:26:25 +0100</pubDate>
            <guid isPermaLink="false">5660891</guid>        </item>
        <item>
            <title>Positron emission tomography imaging in neurological disorders</title>
            <link>http://www.medworm.com/index.php?rid=5660892&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F97j523810qt4121x%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Positron emission tomography (PET) is a powerful tool for in vivo imaging investigations of human brain function. It provides
 non-invasive quantification of brain metabolism, receptor binding of various neurotransmitter systems, and alterations in
 regional blood flow. The use of PET in a clinical setting is still limited due to the high costs of cyclotrons and radiochemical
 laboratories. However, once these limitations can be bypassed, PET could aid clinical practice by providing a useful imaging
 technique for the diagnosis, the planning of treatment, and the prediction outcome in various neurological diseases. This
 review aims to explain the PET imaging technique and its applications in neurological disorders such as Parkinson’s disease,
 Huntington’s disease,...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660892</comments>
            <pubDate>Wed, 01 Feb 2012 17:14:15 +0100</pubDate>
            <guid isPermaLink="false">5660892</guid>        </item>
        <item>
            <title>Neurocognitive and atrophic patterns in Parkinson’s disease based on subjective memory complaints</title>
            <link>http://www.medworm.com/index.php?rid=5660893&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh03w78757k5486q4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ample evidence has suggested that individuals with subjective memory complaints are at a higher risk for cognitive decline.
 Nevertheless, the significance of subjective memory complaints in Parkinson’s disease has not been studied until now. We investigated
 whether the patterns of cognitive profiles and gray matter density differed in cognitively normal patients with Parkinson’s
 disease based on the presence of subjective memory complaints. Using a single question with a yes or no answer, cognitively
 normal patients with Parkinson’s disease were classified as with (n&amp;nbsp;=&amp;nbsp;20) or without subjective memory complaints (n&amp;nbsp;=&amp;nbsp;15). Cognitive profiles and gray matter density were examined using standardized neuropsychological tests and voxel-based
 mo...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660893</comments>
            <pubDate>Tue, 31 Jan 2012 07:10:05 +0100</pubDate>
            <guid isPermaLink="false">5660893</guid>        </item>
        <item>
            <title>An exploratory study of activity in veterans with Parkinson’s disease</title>
            <link>http://www.medworm.com/index.php?rid=5660895&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg516811v27kj16lw%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Movement disorder specialists have limited information on the specifics of how patients with Parkinson’s disease (PD) spend
 their time. We deemed it important to examine the relationships among activity and daily energy expenditure (DEE), non-motor
 symptoms, and body mass index in veterans with PD who were outpatients at a Veterans Affairs medical center. In this exploratory
 study, we mailed demographic and activity questionnaires and gathered data on 100 patients. Activity was categorized into
 five domains and three intensity levels, and DEE was measured in kilocalories. Light activities accounted for 64.9% of DEE
 (9.1&amp;nbsp;h), moderate activities for 32.9% (2.1&amp;nbsp;h), and vigorous activities for 2.2% (0.1&amp;nbsp;h) of DEE. Television viewing comprised
 10.6% (2...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660895</comments>
            <pubDate>Tue, 31 Jan 2012 07:10:04 +0100</pubDate>
            <guid isPermaLink="false">5660895</guid>        </item>
        <item>
            <title>Isolated vertical ophthalmoplegia caused by bilateral rostroventral midbrain infarction</title>
            <link>http://www.medworm.com/index.php?rid=5660894&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq7134190201n21g1%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-3DOI 10.1007/s00415-012-6417-6Authors
		Hiroya Naruse, Department of Neurology, Tokyo Teishin Hospital, 2-14-23, Fujimi, Chiyoda-ku, Tokyo, 102-8798 JapanYu Nagashima, Department of Neurology, Tokyo Teishin Hospital, 2-14-23, Fujimi, Chiyoda-ku, Tokyo, 102-8798 JapanRisa Maekawa, Department of Neurology, Tokyo Teishin Hospital, 2-14-23, Fujimi, Chiyoda-ku, Tokyo, 102-8798 JapanYasushi Shiio, Department of Neurology, Tokyo Teishin Hospital, 2-14-23, Fujimi, Chiyoda-ku, Tokyo, 102-8798 Japan
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660894</comments>
            <pubDate>Tue, 31 Jan 2012 07:10:04 +0100</pubDate>
            <guid isPermaLink="false">5660894</guid>        </item>
        <item>
            <title>Charles-Prosper Ollivier d’Angers (1796–1845)</title>
            <link>http://www.medworm.com/index.php?rid=5660898&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F791351w41g525407%2F</link>
            <description>Content Type Journal ArticleCategory Pioneers in NeurologyPages 1-2DOI 10.1007/s00415-012-6424-7Authors
		Olivier Walusinski, Brou, 28160 France
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660898</comments>
            <pubDate>Tue, 31 Jan 2012 07:10:02 +0100</pubDate>
            <guid isPermaLink="false">5660898</guid>        </item>
        <item>
            <title>Natalizumab treatment of multiple sclerosis in Spain: results of an extensive observational study</title>
            <link>http://www.medworm.com/index.php?rid=5660897&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff211610651732127%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Natalizumab has been shown to be effective in pivotal clinical trials in multiple sclerosis; however, the patients in whom
 treatment is indicated in clinical practice have a different clinical profile from those included in the clinical trials.
 The aim of this study is therefore to collect data on natalizumab use in everyday clinical practice in Spain. The 86 participating
 centers throughout Spain submitted data on disease characteristics at baseline and after treatment. Valid data were available
 for 1,364 patients (69.3% women, 86.9% with relapsing–remitting disease). Ninety-three percent had received prior therapy
 for multiple sclerosis. For the 825 patients on treatment for at least a year, the annualized relapse rate (ARR) decreased
 from median 2.0 [mean 2.0...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660897</comments>
            <pubDate>Tue, 31 Jan 2012 07:10:02 +0100</pubDate>
            <guid isPermaLink="false">5660897</guid>        </item>
        <item>
            <title>Value of MRI as a surrogate marker for PML in natalizumab long-term therapy</title>
            <link>http://www.medworm.com/index.php?rid=5660896&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy369663041734752%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-012-6426-5Authors
		I. Ayzenberg, Department of Neurology, St. Josef Hospital, Ruhr University Bochum, Bochum, GermanyC. Lukas, Department of Radiology, St. Josef Hospital, Ruhr University Bochum, Bochum, GermanyN. Trampe, Department of Neurology, St. Josef Hospital, Ruhr University Bochum, Bochum, GermanyR. Gold, Department of Neurology, St. Josef Hospital, Ruhr University Bochum, Bochum, GermanyK. Hellwig, Department of Neurology, St. Josef Hospital, Ruhr University Bochum, Bochum, Germany
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660896</comments>
            <pubDate>Tue, 31 Jan 2012 07:10:02 +0100</pubDate>
            <guid isPermaLink="false">5660896</guid>        </item>
        <item>
            <title>Functional consequences of a section of the anterior part of the body of the corpus callosum: evidence from an interhemispheric transcallosal approach</title>
            <link>http://www.medworm.com/index.php?rid=5660899&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6nx655n47h615807%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of this study was to determine the neuropsychological consequences of a middle interhemispheric approach for the removal
 of tumors of the third or lateral ventricles. A retrospective analysis of eight callosotomized patients for ventricular tumors
 (three males/five females; mean age: 48.7&amp;nbsp;±&amp;nbsp;11.2&amp;nbsp;years; education level: 11.9&amp;nbsp;±&amp;nbsp;2.9&amp;nbsp;years) and eight healthy subjects was
 performed. An extensive neuropsychological test battery was used to evaluate global intellectual efficiency, memory capacities,
 executive functions, and interhemispheric transfer of a procedural learning task (serial reaction time task/SRTT). Neuropsychological
 results showed that: (1) five of eight patients operated through a middle transcallosal approach had di...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660899</comments>
            <pubDate>Tue, 31 Jan 2012 07:10:01 +0100</pubDate>
            <guid isPermaLink="false">5660899</guid>        </item>
        <item>
            <title>Susceptibility to pattern glare following stroke</title>
            <link>http://www.medworm.com/index.php?rid=5660900&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fwnu152l8hx177524%2F</link>
            <description>This study demonstrates an association between stroke subjects and elevated levels of pattern glare. Cortical
 hyperexcitability has been shown to present following stroke, and this has been proposed as a plausible explanation for the
 perceptual distortions experienced by individuals susceptible to pattern glare. Further work to assess the benefits of spectral
 filters in reducing perceptual distortions in stroke patients is currently underway.
 
 
	Content Type Journal ArticleCategory Original CommunicationPages 1-8DOI 10.1007/s00415-012-6418-5Authors
		Ian G. Beasley, Ophthalmic Research Group, Life and Health Sciences, Aston University, Birmingham, B4 7ET UKLeon N. Davies, Ophthalmic Research Group, Life and Health Sciences, Aston University, Birmingham, B4 7ET UK
	

	
		Journal Journa...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660900</comments>
            <pubDate>Tue, 31 Jan 2012 07:10:00 +0100</pubDate>
            <guid isPermaLink="false">5660900</guid>        </item>
        <item>
            <title>Is cerebral white matter involvement helpful in the diagnosis of dentatorubral-pallidoluysian atrophy?</title>
            <link>http://www.medworm.com/index.php?rid=5650059&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh72r7263212g2qmx%2F</link>
            <description>We describe three cases
 of genetically confirmed DRPLA that developed changes in cerebral white matter in the early stage of middle-aged patients.
 Our results of our study indicate that cerebral white matter changes are not rare in DRPLA and might be helpful for differentiation
 in ataxia patients with brainstem and cerebellum atrophy.
 
 
	Content Type Journal ArticleCategory Original CommunicationPages 1-4DOI 10.1007/s00415-011-6401-6Authors
		Won Tae Yoon, Department of Neurology, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Republic of KoreaJinyoung Youn, Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Ilwon-Dong, Gangnam-Gu, Seoul, 135-710 Republic of KoreaJin Whan Cho, Department of Neurology, Samsung M...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650059</comments>
            <pubDate>Fri, 27 Jan 2012 17:56:41 +0100</pubDate>
            <guid isPermaLink="false">5650059</guid>        </item>
        <item>
            <title>Abnormal sensory-motor integration in a patient with anti-NMDA-receptor encephalitis</title>
            <link>http://www.medworm.com/index.php?rid=5650060&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1475717131462624%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-4DOI 10.1007/s00415-012-6422-9Authors
		Yi-Hsuan Dou, Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, 112 Taipei, TaiwanKuan-Lin Lai, Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, 112 Taipei, TaiwanKwong-Kum Liao, Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, 112 Taipei, TaiwanShih-Pin Chen, Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, 112 Taipei, Taiwan
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650060</comments>
            <pubDate>Fri, 27 Jan 2012 17:56:40 +0100</pubDate>
            <guid isPermaLink="false">5650060</guid>        </item>
        <item>
            <title>Towards understanding seasonal variability in cervical artery dissection (CeAD)</title>
            <link>http://www.medworm.com/index.php?rid=5650061&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg8n2317773002813%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cervical artery dissection (CeAD) occurs more often in autumn or winter than in spring or summer. We searched for clinical
 variables associated with this seasonality by comparing CeAD patients with onset of symptoms in autumn–winter (September 22–March
 21) versus those with first CeAD symptom in spring–summer (March 22–September 21). We performed a cross-sectional study using
 data from the multicenter CADISP (Cervical Artery Dissection and Ischemic Stroke Patients) registry. Age- and sex-matched
 patients with ischemic stroke attributable to a cause other than CeAD (non-CeAD patients) were analyzed to study the specificity
 of our findings. Autumn–winter CeAD patients had a higher median brachial pulse pressure at admission (55 vs. 52&amp;nbsp;mmHg; p&amp;nbsp;=&amp;nb...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650061</comments>
            <pubDate>Fri, 27 Jan 2012 17:56:39 +0100</pubDate>
            <guid isPermaLink="false">5650061</guid>        </item>
        <item>
            <title>Cerebrospinal fluid and lumbar puncture: a practical review</title>
            <link>http://www.medworm.com/index.php?rid=5639505&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F48867658032h4480%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cerebrospinal fluid is vital for normal brain function. Changes to the composition, flow, or pressure can cause a variety
 of neurological symptoms and signs. Equally, disorders of nervous tissue may alter cerebrospinal fluid characteristics. Analysis
 of cerebrospinal fluid can provide information on diagnosis, may be therapeutic in certain conditions, and allows a research
 opportunity into neurological disease. However, inappropriate sampling, inaccurate technique, and incomplete analysis can
 contribute to significant patient morbidity, and reduce the amount of accurate information obtained. In this article, we will
 review how cerebrospinal fluid is produced, circulated, and resorbed. We will also review lumbar puncture technique, equipment,
 and cerebrospinal flui...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639505</comments>
            <pubDate>Wed, 25 Jan 2012 18:13:22 +0100</pubDate>
            <guid isPermaLink="false">5639505</guid>        </item>
        <item>
            <title>The contribution of posterior circulation to memory function during the intracarotid amobarbital procedure</title>
            <link>http://www.medworm.com/index.php?rid=5650062&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk02511n006q75m14%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The purpose of this study was to evaluate the contribution of posterior circulation to memory function by comparing memory
 scores between patients with and without a foetal-type posterior cerebral artery (FTP) during the intracarotid amobarbital
 procedure (IAP) in epilepsy patients. Patients undergoing bilateral IAP between January 2004 and January 2010 were retrospectively
 included. Pre-test angiograms were assessed for the presence of a FTP. Memory function scores (% correct) after right and
 left injections were obtained. Functional significance of FTP was affirmed by relative occipital versus parietal EEG slow-wave
 increase during IAP. Memory and EEG scores were compared between patients with and without FTP (Mann–Whitney U test). A total of 106&amp;nbsp;patients ...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650062</comments>
            <pubDate>Wed, 25 Jan 2012 18:13:21 +0100</pubDate>
            <guid isPermaLink="false">5650062</guid>        </item>
        <item>
            <title>Substance abuse may be a risk factor for earlier onset of Huntington disease</title>
            <link>http://www.medworm.com/index.php?rid=5639506&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg44631l848x5l7g2%2F</link>
            <description>This study investigated the relationships between alcohol, drug, and tobacco abuse and HD age of
 onset in 136 participants with symptomatic HD. CAG repeat length was used as a covariate in all analyses, as it represents
 the most significant determinant of HD age of onset. The relationship between substance abuse, HD age of onset, and sex was
 also examined, as women may experience greater medical harm from substance abuse. Lifetime alcohol abuse and lifetime drug
 abuse were associated with earlier age of HD onset; a similar trend was seen for current tobacco abuse. For women, lifetime
 alcohol abuse was associated with earlier onset of HD, with a similar trend for lifetime drug abuse. However, alcohol, drug,
 and tobacco abuse were not significantly associated with age of onset in men. ...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639506</comments>
            <pubDate>Tue, 24 Jan 2012 18:09:48 +0100</pubDate>
            <guid isPermaLink="false">5639506</guid>        </item>
        <item>
            <title>Hematoma of Meckel’s cave: a rare possible symptomatic trigeminal neuralgia</title>
            <link>http://www.medworm.com/index.php?rid=5639507&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy02utx17jk8174j7%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-012-6410-0Authors
		F. Maggioni, Department of Neurosciences, Headache Centre, University of Padua, Via Giustiniani 5, 35128 Padua, ItalyM. Bellamio, Department of Neurosciences, Headache Centre, University of Padua, Via Giustiniani 5, 35128 Padua, ItalyM. Margoni, Department of Neurosciences, Headache Centre, University of Padua, Via Giustiniani 5, 35128 Padua, ItalyG. Zanchin, Department of Neurosciences, Headache Centre, University of Padua, Via Giustiniani 5, 35128 Padua, ItalyR. Manara, Neuroradiology Unit, University of Padua, Padua, Italy
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639507</comments>
            <pubDate>Tue, 24 Jan 2012 18:09:46 +0100</pubDate>
            <guid isPermaLink="false">5639507</guid>        </item>
        <item>
            <title>Mandibuloptosis as a cause of supine choking in a patient with amyotrophic lateral sclerosis</title>
            <link>http://www.medworm.com/index.php?rid=5639510&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw468356prujuw381%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-012-6416-7Authors
		Michito Namekawa, Department of Neurology, Jichi Medical University, 3311-1, Yakushiji, Shimotsuke, Tochigi, JapanHiroto Ito, Department of Oral and Maxillofacial Surgery, Jichi Medical University, Tochigi, JapanTomoaki Kameda, Department of Neurology, Jichi Medical University, 3311-1, Yakushiji, Shimotsuke, Tochigi, JapanImaharu Nakano, Department of Neurology, Jichi Medical University, 3311-1, Yakushiji, Shimotsuke, Tochigi, Japan
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639510</comments>
            <pubDate>Tue, 24 Jan 2012 18:09:45 +0100</pubDate>
            <guid isPermaLink="false">5639510</guid>        </item>
        <item>
            <title>Techniques and applications of EMG: measuring motor units from structure to function</title>
            <link>http://www.medworm.com/index.php?rid=5639509&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn8g8222n85k13240%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Needle electromyography (EMG) is an established method of evaluating motor unit and muscle fibre function and pathology in
 clinical practice, while the development of advanced techniques including single-fibre EMG and combined recordings with other
 modalities have become increasingly useful in research. The development of quantitative EMG in particular had led to greater
 reproducibility and inter-rater reliability. This review provides an overview of standard needle EMG as well as discussing
 advanced recording and analysis techniques and their increasing role in clinical research.
 
 
	Content Type Journal ArticleCategory Techniques in Clinical SciencePages 1-10DOI 10.1007/s00415-011-6350-0Authors
		Rachel C. Thornton, Department of Clinical Neuroscience, Addenbrook...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639509</comments>
            <pubDate>Tue, 24 Jan 2012 18:09:45 +0100</pubDate>
            <guid isPermaLink="false">5639509</guid>        </item>
        <item>
            <title>Diagnostic yield and predictive value of provoked ictal SPECT in drug-resistant epilepsies</title>
            <link>http://www.medworm.com/index.php?rid=5639508&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx02105p3n2734666%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Brain single photon emission computed tomography (SPECT) can be a useful tool to identify the epileptogenic zone in selected
 patients. However, ictal SPECT during spontaneous seizures is difficult to obtain and can be expensive, due to extra hospitalization
 time and personnel resource utilization. The efficacy of ictal SPECT depends on the ability to inject as early as possible
 after the beginning of the ictal discharge and/or the occurrence of the first symptom and is challenged by the short duration
 and rapid propagation of seizures, especially extratemporal seizures. We studied 52 patients with drug-resistant epilepsy
 who underwent ictal SPECT during provoked seizures in order to demonstrate the efficacy of this technique to define the epileptogenic
 zone and it...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639508</comments>
            <pubDate>Tue, 24 Jan 2012 18:09:45 +0100</pubDate>
            <guid isPermaLink="false">5639508</guid>        </item>
        <item>
            <title>Falling too Fahr</title>
            <link>http://www.medworm.com/index.php?rid=5639511&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F21jn360m87313621%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-012-6411-zAuthors
		Arianna Merlini, Department of Neurology and Neurophysiology, Institute of Experimental Neurology, San Raffaele Scientific Institute, Via Olgettina 58, 20132 Milan, ItalyLuca Peruzzotti-Jametti, Department of Neurology and Neurophysiology, Institute of Experimental Neurology, San Raffaele Scientific Institute, Via Olgettina 58, 20132 Milan, ItalyMarco Bacigaluppi, Department of Neurology and Neurophysiology, Institute of Experimental Neurology, San Raffaele Scientific Institute, Via Olgettina 58, 20132 Milan, ItalyGiovanna Mantovani, Endocrinology and Diabetology Unit, Department of Medical Sciences, Università degli Studi di Milano, Fondazione IRCCS Ca’ Granda Ospedale Maggiore P...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639511</comments>
            <pubDate>Tue, 24 Jan 2012 07:27:55 +0100</pubDate>
            <guid isPermaLink="false">5639511</guid>        </item>
        <item>
            <title>Validation of the Comprehensive International Classification of Functioning, Disability, and Health Core Set for multiple sclerosis from the perspective of physicians</title>
            <link>http://www.medworm.com/index.php?rid=5639513&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh7647787g0681441%2F</link>
            <description>The objective of this
 study was to validate the Comprehensive ICF Core Set for MS from the perspective of physicians. Using a three-round Delphi
 technique, physicians experienced in the MS treatment were requested to name patients’ problems, resources, and aspects of
 environment. The statements of the first Delphi round were linked to ICF categories based on established linking rules. These
 categories as well as the results of the second round were reported back to the participants. Eighty-four physicians participated
 in the study. Totally, 89 categories (64.5%) of the Comprehensive ICF Core Set for MS were confirmed by the participants.
 Eight ICF categories, which are currently not included in the ICF Core Set, were identified. The validity of the Comprehensive
 ICF Core Set for M...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639513</comments>
            <pubDate>Tue, 24 Jan 2012 07:27:54 +0100</pubDate>
            <guid isPermaLink="false">5639513</guid>        </item>
        <item>
            <title>Polyneuropathy while on duodenal levodopa infusion in Parkinson’s disease patients: we must be alert</title>
            <link>http://www.medworm.com/index.php?rid=5639512&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr3116u102xr41731%2F</link>
            <description>We describe
 five PD patients who developed axonal polyneuropathy and vitamin B12 deficiency while on treatment with duodenal levodopa infusion, review other cases reported in the literature, discuss potential
 etiologic factors, and suggest a possible algorithm for the management and prevention of this complication. One case of Guillain-Barré
 syndrome and at least 12 cases of polyneuropathy related to vitamin B12 deficiency have been reported in PD patients treated with duodenal levodopa infusion. Levodopa gel infusion may induce a
 decrease in vitamin B12 levels, leading to peripheral neuropathy. Additional pathogenetic mechanisms include alterations related to the metabolism
 of l-dopa, abnormal l-dopa absorption, and direct neurotoxicity of l-dopa at high doses. Vitamin B12 supplemen...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639512</comments>
            <pubDate>Tue, 24 Jan 2012 07:27:54 +0100</pubDate>
            <guid isPermaLink="false">5639512</guid>        </item>
        <item>
            <title>Fractional anisotropy in the centrum semiovale as a quantitative indicator of cerebral white matter damage in the subacute phase in patients with carbon monoxide poisoning: correlation with the concentration of myelin basic protein in cerebrospinal fluid</title>
            <link>http://www.medworm.com/index.php?rid=5621271&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq5m232347trl0204%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Carbon monoxide (CO) poisoning leads to demyelination of cerebral white matter (CWM) fibers, causing chronic neuropsychiatric
 symptoms. To clarify whether fractional anisotropy (FA) from diffusion tensor imaging in the centrum semiovale can depict
 demyelination in the CWM during the subacute phase after CO inhalation, we examined correlations between FA in the centrum
 semiovale and myelin basic protein (MBP) in cerebrospinal fluid. Subjects comprised 26 adult CO-poisoned patients ≤60&amp;nbsp;years
 old. MBP concentration was examined for all patients at 2&amp;nbsp;weeks after CO inhalation. The mean FA of the centrum semiovale
 bilaterally at 2&amp;nbsp;weeks was also examined for all patients and 21 age-matched healthy volunteers as controls. After these examinations,
 the p...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5621271</comments>
            <pubDate>Thu, 19 Jan 2012 06:51:49 +0100</pubDate>
            <guid isPermaLink="false">5621271</guid>        </item>
        <item>
            <title>Progress in cerebrovascular disease research in the last year</title>
            <link>http://www.medworm.com/index.php?rid=5621272&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fgw286pl548155r65%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Herein, we review the main papers in cerebrovascular diseases published in the Journal of Neurology over the last year.
 
 
	Content Type Journal ArticleCategory Medical Progress in the Journal of NeurologyPages 1-4DOI 10.1007/s00415-012-6408-7Authors
		Sergio Amaro, Comprehensive Stroke Center, Hospital Clinic, University of Barcelona, Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), 170 Villarroel, 08036 Barcelona, SpainAngel Chamorro, Comprehensive Stroke Center, Hospital Clinic, University of Barcelona, Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), 170 Villarroel, 08036 Barcelona, Spain
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5621272</comments>
            <pubDate>Thu, 19 Jan 2012 06:51:48 +0100</pubDate>
            <guid isPermaLink="false">5621272</guid>        </item>
        <item>
            <title>Verbal and nonverbal memory impairment in aphasia</title>
            <link>http://www.medworm.com/index.php?rid=5621273&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy2u18306763062vw%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Repetition is frequently impaired in aphasia, most strikingly in conduction aphasia. The still not fully answered question
 is whether this relates to a linguistic deficit or to a general impairment of working memory extending to other modalities
 as well. To contribute to this problem, we assessed 49 aphasic and 50 non-aphasic stroke patients using an aphasia test plus
 three memory tests in forward and backward fashion, taxing verbal, numerical, spatial, and facial retention. The results show
 that in aphasics there is a memory gradient declining gradually from verbal to nonverbal content reflecting aphasia severity
 and that aphasics generally perform worse than non-aphasics, even if they present with similar cerebral lesions.
 
 
	Content Type Journal ArticleCategor...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5621273</comments>
            <pubDate>Thu, 19 Jan 2012 06:51:47 +0100</pubDate>
            <guid isPermaLink="false">5621273</guid>        </item>
        <item>
            <title>Improving survival in a large French ALS center cohort</title>
            <link>http://www.medworm.com/index.php?rid=5621274&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F71553m7448034820%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of this work was to determine whether survival changed during 2002–2009 at a French amyotrophic lateral sclerosis
 (ALS) center. We included all patients with ALS who were seen consecutively at the center from January 2002–May 2009. Participants
 were followed from date of first visit through death, date of censoring, or December 31, 2009, whichever occurred first. Cox
 proportional hazard models computed hazard ratios (HR; 95% confidence interval CI) of death, and flexible modeling of continuous
 predictors (splines) assessed trends in survival. We analyzed a total of 2,037 ALS patients, of whom 1,471 died before the
 end of follow-up. Median survival was 2.83&amp;nbsp;years from onset and 1.65&amp;nbsp;years from first visit. Compared to patients first seen
 befor...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5621274</comments>
            <pubDate>Thu, 19 Jan 2012 06:51:46 +0100</pubDate>
            <guid isPermaLink="false">5621274</guid>        </item>
        <item>
            <title>Patterns of white matter diffusivity abnormalities in Leber’s hereditary optic neuropathy: a tract-based spatial statistics study</title>
            <link>http://www.medworm.com/index.php?rid=5611118&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc487693615v70v56%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Leber’s hereditary optic neuropathy (LHON) is a mitochondrial disease characterized by retinal ganglion cell degeneration
 and optic nerve atrophy, leading to a loss of central vision. The aim of this study was to explore the topographical pattern
 of damage to the brain white matter (WM) tracts from patients with chronic LHON using diffusion tensor (DT) MRI and tract-based
 spatial statistics (TBSS). Brain dual-echo and DT MRI scans were acquired from 13 patients with chronic LHON and 25 matched
 controls using a 3.0&amp;nbsp;T scanner. TBSS analysis was performed using the FMRIB’s Diffusion Toolbox. A complete neuro-ophthalmologic
 examination, including standardized automated Humphrey perimetry as well as average and temporal peripapillary retinal nerve
 fiber layer ...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611118</comments>
            <pubDate>Tue, 17 Jan 2012 07:12:51 +0100</pubDate>
            <guid isPermaLink="false">5611118</guid>        </item>
        <item>
            <title>White matter lesions and intra-arterial thrombolysis</title>
            <link>http://www.medworm.com/index.php?rid=5611117&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F52t2112424452l56%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of the study was to assess the influence of white matter lesions in patients with acute ischemic stroke treated with
 intra-arterial thrombolysis (IAT). From September 2003 to January 2010, we treated 400 patients with IAT at our institution.
 Of these patients, 292 were evaluated with MRI scans and included in this observational study. Clinical data were collected
 prospectively. Outcome after 3&amp;nbsp;months was measured with the modified Rankin Scale (mRS); mRS 0–1 was considered as favorable
 outcome. White matter lesions were scored visually by two observers using the semiquantitative Scheltens and Fazekas scores.
 Logistic regression analysis was used to identify the association of white matter lesions and clinical outcome, recanalization,
 and cerebral he...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611117</comments>
            <pubDate>Tue, 17 Jan 2012 07:12:51 +0100</pubDate>
            <guid isPermaLink="false">5611117</guid>        </item>
        <item>
            <title>Increased cerebral activation after behavioral treatment for memory deficits in MS</title>
            <link>http://www.medworm.com/index.php?rid=5599367&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp0357631248h32m2%2F</link>
            <description>This study is the first to demonstrate a significant change in cerebral activation
 resulting from a behavioral memory intervention in an MS sample. Behavioral interventions can show significant changes in
 the brain, validating clinical utility.
 
 
	Content Type Journal ArticleCategory Original CommunicationPages 1-10DOI 10.1007/s00415-011-6353-xAuthors
		Nancy D. Chiaravalloti, Kessler Foundation Research Center, West Orange, NJ, USAGlenn Wylie, Kessler Foundation Research Center, West Orange, NJ, USAVictoria Leavitt, Kessler Foundation Research Center, West Orange, NJ, USAJohn DeLuca, Kessler Foundation Research Center, West Orange, NJ, USA
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5599367</comments>
            <pubDate>Thu, 12 Jan 2012 06:42:17 +0100</pubDate>
            <guid isPermaLink="false">5599367</guid>        </item>
        <item>
            <title>The case of the Marquis de Causan (1804): an early account of visual loss associated with spinal cord inflammation</title>
            <link>http://www.medworm.com/index.php?rid=5599366&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy71211tk182m7226%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The recent discovery of disease specific and pathogenic autoantibodies in neuromyelitis optica (NMO, Devic’s disease) has
 revived the interest in this intriguing yet often devastating condition. While the history of classic multiple sclerosis has
 been studied extensively, only very little is known so far about the early history of NMO. Here we discuss a now forgotten
 report by the famous French anatomist and pathologist Antoine Portal (1742–1832), first physician to Louis XVIII and founding
 and lifelong president of the Académie Nationale de Médecine. Portals report, which fascinated some of the most renowned 19th century pioneers in the field of neurology but fell in oblivion
 later, represents the first account of visual loss in a patient with spinal cord in...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5599366</comments>
            <pubDate>Thu, 12 Jan 2012 06:42:17 +0100</pubDate>
            <guid isPermaLink="false">5599366</guid>        </item>
        <item>
            <title>Rating papilloedema: an evaluation of the Frisén classification in idiopathic intracranial hypertension</title>
            <link>http://www.medworm.com/index.php?rid=5599368&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6u7256511mm21u47%2F</link>
            <description>This study demonstrated the limited reproducibility and discriminative ability of the Frisén classification in
 identifying changes in serial optic disc photographs in IIH. Simple optic disc ranking appears to be a more sensitive and
 reliable tool to monitor changes in optic disc appearance. The use of disc ranking in clinical practice and research studies
 is recommended to monitor alterations in optic disc appearance until alternative schemes, specific to IIH, have been developed.
 
 
	Content Type Journal ArticleCategory Original CommunicationPages 1-7DOI 10.1007/s00415-011-6365-6Authors
		Alexandra J. Sinclair, Neurobiology and Neuropharmacology, School of Clinical and Experimental Medicine, College of Medical and Dental Sciences, University of Birmingham, Wolfson Drive, Edgbaston, B...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5599368</comments>
            <pubDate>Thu, 12 Jan 2012 06:42:15 +0100</pubDate>
            <guid isPermaLink="false">5599368</guid>        </item>
        <item>
            <title>Gender-related differences in the burden of non-motor symptoms in Parkinson’s disease</title>
            <link>http://www.medworm.com/index.php?rid=5584662&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1w55167l277r9w36%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Differences in the expression of non-motor symptoms (NMS) by Parkinson’s disease (PD) patients may have important implications
 for their management and prognosis. Gender is a basic epidemiological variable that could influence such expression. The present
 study evaluated the prevalence and severity of NMS by gender in an international sample of 951 PD patients, 62.63% males,
 using the non-motor symptoms scale (NMSS). Assessments for motor impairment and complications, global severity, and health
 state were also applied. All disease stages were included. No significant gender differences were found for demographic and
 clinical characteristics. For the entire sample, the most prevalent symptoms were Nocturia (64.88%) and Fatigue (62.78%) and
 the most prevalent aff...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5584662</comments>
            <pubDate>Wed, 11 Jan 2012 17:55:52 +0100</pubDate>
            <guid isPermaLink="false">5584662</guid>        </item>
        <item>
            <title>Delirium in acute stroke: screening tools, incidence rates and predictors: a systematic review</title>
            <link>http://www.medworm.com/index.php?rid=5584663&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd41530h7u175u744%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Delirium is a common complication in acute stroke yet there is uncertainty regarding how best to screen for and diagnose delirium
 after stroke. We sought to establish how delirium after stroke is identified, its incidence rates and factors predicting its
 development. We conducted a systematic review of studies investigating delirium in acute stroke. We searched The Cochrane
 Collaboration, MEDLINE, EMBASE, CINHAL, PsychINFO, Web of Science, British Nursing Index, PEDro and OT Seeker in October 2010.
 A total of 3,127 citations were screened, full text of 60 titles and abstracts were read, of which 20 studies published between
 1984 and 2010 were included in this review. The methods most commonly used to identify delirium were generic assessment tools
 such as the Deli...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5584663</comments>
            <pubDate>Wed, 11 Jan 2012 06:56:55 +0100</pubDate>
            <guid isPermaLink="false">5584663</guid>        </item>
        <item>
            <title>History of the ‘geste antagoniste’ sign in cervical dystonia</title>
            <link>http://www.medworm.com/index.php?rid=5584664&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu6527227m4574373%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The geste antagoniste is a voluntary maneuver that temporarily reduces the severity of dystonic posture or movements. It is a classical feature
 of focal and particularly cervical dystonia. However, the precise historical aspects of geste antagoniste still remain obscure. The goals of this review were (1) to clarify the origin of the geste antagoniste sign; (2) to identify the factors that led to its diffusion in the international literature; (3) to follow the evolution
 of that term across the twentieth century. We used medical and neurological French, German and English literature of the late
 nineteenth and early twentieth centuries, and the PubMed database by entering the terms geste antagoniste, antagonistic gesture and sensory trick. The geste antagoniste sign is ...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5584664</comments>
            <pubDate>Wed, 11 Jan 2012 06:56:53 +0100</pubDate>
            <guid isPermaLink="false">5584664</guid>        </item>
        <item>
            <title>Erratum to: Transcranial sonography in pantothenate kinase-associated neurodegeneration</title>
            <link>http://www.medworm.com/index.php?rid=5584666&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu27551k4l56u0586%2F</link>
            <description>Content Type Journal ArticleCategory ErratumPages 1-1DOI 10.1007/s00415-012-6409-6Authors
		Vladimir S. Kostić, School of Medicine, Institute of Neurology CCS, University of Belgrade, Ul. Dr Subotića 6, 11000 Belgrade, SerbiaMarina Svetel, School of Medicine, Institute of Neurology CCS, University of Belgrade, Ul. Dr Subotića 6, 11000 Belgrade, SerbiaMilija Mijajlović, School of Medicine, Institute of Neurology CCS, University of Belgrade, Ul. Dr Subotića 6, 11000 Belgrade, SerbiaAleksandra Pavlović, School of Medicine, Institute of Neurology CCS, University of Belgrade, Ul. Dr Subotića 6, 11000 Belgrade, SerbiaMilica Ječmenica-Lukić, School of Medicine, Institute of Neurology CCS, University of Belgrade, Ul. Dr Subotića 6, 11000 Belgrade, SerbiaDuško Kozić, School of Medicin...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5584666</comments>
            <pubDate>Tue, 10 Jan 2012 17:02:00 +0100</pubDate>
            <guid isPermaLink="false">5584666</guid>        </item>
        <item>
            <title>Interleukin-1A −889C/T polymorphism and risk of Alzheimer’s disease: a meta-analysis based on 32 case–control studies</title>
            <link>http://www.medworm.com/index.php?rid=5584665&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl01n202182517366%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The Interleukin-1A (IL-1A) −889C/T polymorphism has been reported to be associated with Alzheimer’s disease (AD) susceptibility, but the results of
 these previous studies have been inconsistent. The aim of this study was to explore whether the IL-1A −889C/T polymorphism confers susceptibility to AD. All studies published up to July 2011 on the association between the IL-1A −889C/T polymorphism and AD risk were identified by searching electronic databases PubMed, Embase and Alzgene. The association
 between the IL-1A −889C/T polymorphism and AD risk was assessed by odds ratios (ORs) together with their 95% confidence intervals (CIs). A
 total of 32 case–control studies including 7,046 AD cases and 7,534 controls were eventually identified. Overall, positive
...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5584665</comments>
            <pubDate>Tue, 10 Jan 2012 17:02:00 +0100</pubDate>
            <guid isPermaLink="false">5584665</guid>        </item>
        <item>
            <title>Temporal trend of amyotrophic lateral sclerosis incidence in southern Europe: a population study in the health district of Ferrara, Italy</title>
            <link>http://www.medworm.com/index.php?rid=5584667&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F92n4r32w18426p57%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Data about the temporal trend of amyotrophic lateral sclerosis (ALS) incidence in southern Europe are scarce. Incidence studies
 on ALS have been carried out in the health district of Ferrara, Italy, since 1960s. We expanded the previous studies from
 1964 to 2009. The study was prospective with a subsequent retrospective intensive survey of multiple sources of case ascertainment.
 All patients with a definite and probable ALS according to the original El Escorial criteria were selected. There were 130
 incident cases in the years 1964–2009 giving an average annual crude incidence of 1.82 per 100,000 population (95% CI 1.53–2.17).
 An incidence increase during the study period was estimated in women (χ2 test for trend&amp;nbsp;=&amp;nbsp;7.19, p&amp;nbsp;&amp;lt;&amp;nbsp;0.01) and in...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5584667</comments>
            <pubDate>Tue, 10 Jan 2012 06:48:23 +0100</pubDate>
            <guid isPermaLink="false">5584667</guid>        </item>
        <item>
            <title>Muscle imaging findings in GNE myopathy</title>
            <link>http://www.medworm.com/index.php?rid=5584670&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff83h7j2v448l6325%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;GNE myopathy (MIM 600737) is an autosomal recessive muscle disease caused by mutations in the UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) gene. Besides the typical phenotype, characterized by the initial involvement of the distal leg muscles that eventually
 spreads proximally with sparing of the quadriceps, uncommon presentations with a non-canonical clinical phenotype, unusual
 muscle biopsy findings or both are increasingly recognized. The aim of our study was to characterize the imaging pattern of
 pelvic and lower limb muscles in GNE myopathy, thus providing additional diagnostic clues useful in the identification of
 patients with atypical features. We retrospectively evaluated muscle MRI and CT scans of a cohort of 13 patients heterogeneo...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5584670</comments>
            <pubDate>Tue, 10 Jan 2012 06:48:22 +0100</pubDate>
            <guid isPermaLink="false">5584670</guid>        </item>
        <item>
            <title>Semantic dementia associated with corticobasal syndrome: a further variant of frontotemporal lobe degeneration?</title>
            <link>http://www.medworm.com/index.php?rid=5584669&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy841r3lp3g1m06l3%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-3DOI 10.1007/s00415-011-6389-yAuthors
		Simona Luzzi, Dipartimento di Medicina Clinica e Sperimentale, Clinica Neurologica, Università Politecnica delle Marche-Ospedali Riuniti di Ancona, Via Conca, 1, Torrette di Ancona, ItalyViviana Cafazzo, Dipartimento di Medicina Clinica e Sperimentale, Clinica Neurologica, Università Politecnica delle Marche-Ospedali Riuniti di Ancona, Via Conca, 1, Torrette di Ancona, ItalyMauro Silvestrini, Dipartimento di Medicina Clinica e Sperimentale, Clinica Neurologica, Università Politecnica delle Marche-Ospedali Riuniti di Ancona, Via Conca, 1, Torrette di Ancona, ItalyLeandro Provinciali, Dipartimento di Medicina Clinica e Sperimentale, Clinica Neurologica, Università Politecnica delle...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5584669</comments>
            <pubDate>Tue, 10 Jan 2012 06:48:22 +0100</pubDate>
            <guid isPermaLink="false">5584669</guid>        </item>
        <item>
            <title>REM sleep behavior disorder in Japanese patients with Parkinson’s disease: a multicenter study using the REM sleep behavior disorder screening questionnaire</title>
            <link>http://www.medworm.com/index.php?rid=5584668&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F01w0v4426vjtn508%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;REM sleep behavior disorder (RBD) is known to be observed more frequently in patients with an α-synucleinopathy such as Parkinson’s
 disease (PD) than in the general population. The precise prevalence of RBD in Japanese PD patients is not known. Therefore,
 we investigated the prevalence and the clinical characteristics of patients with RBD in a large population of Japanese patients
 with PD. We investigated various clinical features and employed the Japanese version of the RBD screening questionnaire on
 469 non-demented Japanese PD patients in this multicenter study. Probable or possible RBD was detected in 146 patients (31.1%)
 and was significantly associated with longer PD duration, higher Hoehn and Yahr stage, higher Unified Parkinson’s Disease
 Rating Scale ...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5584668</comments>
            <pubDate>Tue, 10 Jan 2012 06:48:22 +0100</pubDate>
            <guid isPermaLink="false">5584668</guid>        </item>
        <item>
            <title>How to identify stroke mimics in patients eligible for intravenous thrombolysis?</title>
            <link>http://www.medworm.com/index.php?rid=5584672&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx77845289x16343p%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Since decision-making for thrombolysis in acute stroke settings is restricted to a limited time window and based on clinical
 assessment and CT findings only, thrombolysis is sometimes applied to patients with a final diagnosis other than a stroke.
 From a prospectively collected stroke/MRI data bank (2004–2010) with 648 suspected ischemic stroke patients treated with rtPA,
 we identified patients without evidence of acute infarction on follow-up MRI and a final diagnosis other than a stroke or
 acute cerebrovascular event. We compared demographics, symptoms, complications, and outcome of patients with stroke mimics
 (SM) to those with acute infarction. In 42 patients, an SM was diagnosed: seizures in 20, conversion disorder in seven, dementia
 in six, migraine in thr...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5584672</comments>
            <pubDate>Tue, 10 Jan 2012 06:48:21 +0100</pubDate>
            <guid isPermaLink="false">5584672</guid>        </item>
        <item>
            <title>Growth-differentiation factor-15 and functional outcome after acute ischemic stroke</title>
            <link>http://www.medworm.com/index.php?rid=5584671&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F719277jh2422020u%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Blood biomarkers may improve the performance in predicting early stroke outcome beyond well-established clinical factors.
 We investigated the value of growth-differentiation factor-15 (GDF-15) to predict functional outcome after 90&amp;nbsp;days in a prospectively
 collected patient cohort with symptoms of acute ischemic stroke. Two hundred eighty-one patients with symptoms of acute ischemic
 stroke were prospectively investigated. Serial blood samples for GDF-15 analysis were obtained after the admission of the
 patient, after 6 and 24&amp;nbsp;h. Primary outcome was the dichotomized modified ranking scale (MRS) 90&amp;nbsp;days after the initial clinical
 event. Within the final study population (264 patients, mean age 70.3&amp;nbsp;±&amp;nbsp;12.7&amp;nbsp;years, 55.3% male), National Ins...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5584671</comments>
            <pubDate>Tue, 10 Jan 2012 06:48:21 +0100</pubDate>
            <guid isPermaLink="false">5584671</guid>        </item>
        <item>
            <title>Social, societal, and economic burden of mal de debarquement syndrome</title>
            <link>http://www.medworm.com/index.php?rid=5584673&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh891108x73220207%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Mal de debarquement syndrome (MdDS) is a disorder of phantom perception of self-motion of unknown cause. The purpose of this
 work was to describe the quality of life (QOL) of patients with MdDS and to estimate the economic costs associated with this
 disorder. A modified version of a QOL survey used for another neurological disease (multiple sclerosis; MSQOL-54) was used
 to assess the impact of MdDS on QOL in 101 patients. The estimated economic costs were based on self-reported direct and indirect
 costs of individuals living in the United States using Medicare reimbursement payment rates for 2011 in 79 patients. Patients
 with MdDS reported a poor overall QOL as indicated by a mean composite QOL score of 59.26&amp;nbsp;±&amp;nbsp;1.89 (out of 100). The subcategories
 havin...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5584673</comments>
            <pubDate>Mon, 09 Jan 2012 19:35:32 +0100</pubDate>
            <guid isPermaLink="false">5584673</guid>        </item>
        <item>
            <title>Causes of coma and their evolution in the medical intensive care unit</title>
            <link>http://www.medworm.com/index.php?rid=5584676&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy5028xn35xvm7772%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-4DOI 10.1007/s00415-011-6388-zAuthors
		Nicolas Weiss, Medical Intensive Care Unit, Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, 20, rue Leblanc, Paris, FranceLucille Regard, Medical Intensive Care Unit, Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, 20, rue Leblanc, Paris, FranceCharles Vidal, Medical Intensive Care Unit, Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, 20, rue Leblanc, Paris, FranceYosu Luque, Medical Intensive Care Unit, Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, 20, rue Leblanc, Paris, FranceGuillaume Taldir, Medical Intensive Care Unit, Hôpital Européen Georges Pompidou, Assist...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5584676</comments>
            <pubDate>Mon, 09 Jan 2012 19:35:31 +0100</pubDate>
            <guid isPermaLink="false">5584676</guid>        </item>
        <item>
            <title>Genotype and phenotype study of 34 Spanish patients diagnosed with oculopharyngeal muscular dystrophy</title>
            <link>http://www.medworm.com/index.php?rid=5584675&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8603p63644159824%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Oculopharyngeal muscular dystrophy is an autosomal dominant adult-onset disease with several clinical features. The genetic
 cause is an expanded (GCN)n mutation coding for polyalanine. Severity and the age of onset are variable and may depend on
 the size of the unstable triplet. Our objectives were to correlate the genotypic and phenotypic features in 34 affected patients,
 and to complete the molecular analysis for a control Spanish population in order to confirm the (GCN)n polymorphism frequency
 observed in other populations. We found a correlation between impaired CPK levels and sex. No statistical differences were
 found when comparing the length in triplet expansion and other variables. The (GCN)n polymorphism’s frequency observed in
 other countries could not...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5584675</comments>
            <pubDate>Mon, 09 Jan 2012 19:35:31 +0100</pubDate>
            <guid isPermaLink="false">5584675</guid>        </item>
        <item>
            <title>Does fingolimod in multiple sclerosis patients cause macular edema?</title>
            <link>http://www.medworm.com/index.php?rid=5584674&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fgh7458611455092n%2F</link>
            <description>We report a case of relapsing–remitting
 MS treated with fingolimod. The patient presented with an acute decrease in vision in the left eye. Eye examination showed
 clinical macular edema (ME) in the left eye, which was confirmed on fluorescein angiogram and optical coherence tomography
 (OCT). After discontinuation of fingolimod and treatment with topical corticosteroid medication, there was complete resolution
 of the ME. The ME as a side-effect of fingolimod is reversible after discontinuing, which was seen on OCT.
 
 
	Content Type Journal ArticleCategory Short CommentaryPages 1-3DOI 10.1007/s00415-011-6367-4Authors
		Kiran Turaka, Associated Retina Consultants Ltd, 7600 N 15th Street, Phoenix, AZ 85020, USAJoseph Shepard Bryan, Associated Retina Consultants Ltd, 7600 N 15th Street, ...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5584674</comments>
            <pubDate>Mon, 09 Jan 2012 19:35:31 +0100</pubDate>
            <guid isPermaLink="false">5584674</guid>        </item>
        <item>
            <title>A novel mutation of myelin protein zero associated with late-onset predominantly axonal Charcot-Marie-Tooth disease</title>
            <link>http://www.medworm.com/index.php?rid=5573049&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F274560qr734u7303%2F</link>
            <description>We report a case of late-onset predominantly axonal Charcot-Marie-Tooth disease resulting from a novel mutation in the MPZ gene encoding myelin protein zero (P0). Neurological examination, electrophysiological examination and genetic testing were
 performed on three members of a Finnish family (family A) and one member of a German family (family B). Three other members
 of the Finnish family were interviewed and genetically tested. Genetic testing was also performed on 95 healthy Finnish controls.
 Three members in two generations of family A and the member of family B were affected with late-onset axonal more than demyelinating,
 motor and sensory polyneuropathy. Heterozygous c.316C&amp;gt;T mutation in MPZ leading to p.Arg106Cys in P0 was found in all the affected subjects, but not in the th...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573049</comments>
            <pubDate>Fri, 06 Jan 2012 06:44:46 +0100</pubDate>
            <guid isPermaLink="false">5573049</guid>        </item>
        <item>
            <title>Evolution of MS lesions to black holes under DNA vaccine treatment</title>
            <link>http://www.medworm.com/index.php?rid=5573050&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F933745t55m670570%2F</link>
            <description>The objective
 of this work was to determine if BHT-3009, a DNA plasmid-encoding myelin basic protein (MBP), reduces the risk of new lesions
 becoming PBH, compared to placebo, and to test if pre-treatment serum anti-MBP antibody levels impact on the effect of BHT-3009
 treatment. In this retrospective, blinded MRI study, we reviewed MRI scans of 155 MS patients from a double-blind, randomized,
 phase II trial with three treatment arms (placebo, 0.5 and 1.5&amp;nbsp;mg BHT-3009). New lesions at weeks 8 and 16 were tracked at
 week 48 and those appearing as T1-hypointense were classified as PBH. A subset of 46 patients with available pre-treatment
 serum anti-MBP IgM levels were analyzed separately. Overall, there was no impact of treatment on the risk for PBH. However,
 there was a significant...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573050</comments>
            <pubDate>Fri, 06 Jan 2012 06:44:45 +0100</pubDate>
            <guid isPermaLink="false">5573050</guid>        </item>
        <item>
            <title>Hemifacial spasm: clinical characteristics of 321 Indian patients</title>
            <link>http://www.medworm.com/index.php?rid=5573051&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fqm4356782401464n%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hemifacial spasm (HFS) is a common neurological disorder characterized by involuntary tonic and clonic contractions of the
 muscles innervated by the facial nerve. We aimed to describe clinical features, common antecedents, triggers and relieving
 factors in patients with hemifacial spasm to study the correlation of hypertension and HFS, and to compare clinical features
 of primary and secondary cases of HFS. The data for the study were collected prospectively on a predesigned and pre-tested
 format at the first attendance in all consecutive HFS patients attending the movement disorders clinic of a tertiary teaching
 hospital in India. The demographic profile, HFS symptoms, antecedent illnesses and neurological examination were recorded
 and analyzed. Muscle power in in...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573051</comments>
            <pubDate>Fri, 06 Jan 2012 06:44:41 +0100</pubDate>
            <guid isPermaLink="false">5573051</guid>        </item>
        <item>
            <title>Is adjunctive corticosteroid beneficial in pneumococcal meningitis in a region with high rates of resistance to penicillin and ceftriaxone?</title>
            <link>http://www.medworm.com/index.php?rid=5573052&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0380522071k71325%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The role of adjunctive corticosteroids remains controversial in meningitis by penicillin-resistant pneumococci. We determined
 the effect of adjunctive corticosteroids in adults with pneumococcal meningitis in a region with a high rate of penicillin
 resistance. A multicenter, retrospective cohort study was conducted between 1998 and 2008 in Korea. The mortality and neurological
 sequelae were evaluated. Among 93 patients with pneumococcal meningitis, adequate adjunctive corticosteroids were given in
 45.2%. The penicillin resistance rate was 60.0%, and 42.1% were nonsusceptible to ceftriaxone. The 30-day mortality rates
 in the group receiving adequate corticosteroid therapy, the group in which corticosteroid was not given, and that inadequately
 given were 24.3, 31.6,...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573052</comments>
            <pubDate>Fri, 06 Jan 2012 06:44:39 +0100</pubDate>
            <guid isPermaLink="false">5573052</guid>        </item>
        <item>
            <title>Is there delayed gastric emptying in patients with multiple system atrophy? An analysis using the 13C-acetate breath test</title>
            <link>http://www.medworm.com/index.php?rid=5573054&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyw9335g11557370j%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Autonomic failure is one of the criteria according to the second consensus statement for the diagnosis of multiple system
 atrophy (MSA). Gastrointestinal symptoms are frequent complaints in patients with MSA and may be associated with reduced gastrointestinal
 motility due to autonomic nervous system dysfunction. However, there are few reports on gastric emptying in patients with
 MSA. We investigated gastric emptying in 25 patients with MSA, 20 patients with sporadic adult-onset ataxia of unknown etiology
 (SAOA), and 20 healthy volunteers using the 13C-acetate breath test. Gastric emptying function is estimated by this test as the half-emptying time (HET) and peak time of
 the 13C-%-dose-excess curve (T
 max), with expirations collected for 4&amp;nbsp;h after a test meal...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573054</comments>
            <pubDate>Thu, 05 Jan 2012 06:52:09 +0100</pubDate>
            <guid isPermaLink="false">5573054</guid>        </item>
        <item>
            <title>SOD2 as a potential modifier of X-linked adrenoleukodystrophy clinical phenotypes</title>
            <link>http://www.medworm.com/index.php?rid=5573053&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F035r2w06k48156g1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;X-linked adrenoleukodystrophy (XALD), a neurological disorder caused by mutations in the peroxisomal membrane protein gene
 ABCD1, presents as a rapidly progressing, inflammatory cerebral demyelination (cerebral cases) or a slowly progressing, distal axonopathy
 (non-cerebral cases). Specific ABCD1 defects do not explain this significant phenotypic variation. Patients have increased plasma and tissue very long chain fatty
 acid levels and increased cellular oxidative stress and oxidative damage. Superoxide dismutase 2 (SOD2), at candidate modifier locus 6q25.3, detoxifies superoxide radicals protecting against oxidative stress and damage. We tested
 an SOD2 variant C47T (Ala16Val) associated with reduced enzymatic activity as a potential modifier gene of cerebral demyel...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573053</comments>
            <pubDate>Thu, 05 Jan 2012 06:52:09 +0100</pubDate>
            <guid isPermaLink="false">5573053</guid>        </item>
        <item>
            <title>Different independent susceptibility markers for first-ever cerebral infarction and myocardial infarction in young patients</title>
            <link>http://www.medworm.com/index.php?rid=5573055&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff1821460v0246819%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cerebral infarction (CI) and myocardial infarction (MI) share some common features, but there are other differences in risk
 factors. The aim of our study is to determine whether there are some significantly independent susceptibility markers for
 them. All consecutive patients between the ages of 18 and 45&amp;nbsp;years with first-ever CI and MI during 2001–2010 were recruited
 to participate in the study. Using multivariate logistic regression modeling, we explore many different data, such as age
 at onset, sex ratio, numbers of patients with history of hypertension, smoking, drinking, and serum lipid, uric acid, prealbumin
 (PA), and white blood cell (WBC) count levels. Logistic regression analysis adjusted for confounders confirmed the following
 independent suscepti...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573055</comments>
            <pubDate>Thu, 05 Jan 2012 06:52:08 +0100</pubDate>
            <guid isPermaLink="false">5573055</guid>        </item>
        <item>
            <title>GQ1b-seronegative Fisher syndrome: clinical features and new serological markers</title>
            <link>http://www.medworm.com/index.php?rid=5573057&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6738j5352737w455%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;IgG anti-GQ1b antibodies are a powerful serological marker for the diagnosis of Fisher syndrome (FS), but little is known
 regarding serological markers in FS patients that do not have the autoantibodies. The authors analyzed IgG antibodies against
 gangliosides other than GQ1b, ganglioside complexes, and ganglioside-like lipo-oligosaccharide (LOS) of Campylobacter jejuni isolates from FS patients. We identified 24 (12%) patients with GQ1b-seronegative FS among 207 FS patients who had been referred
 to our laboratory for anti-ganglioside antibody testing. Patients with GQ1b-seronegative FS were male and had a history of
 antecedent gastrointestinal illness more frequently than FS patients with IgG anti-GQ1b antibodies. Other clinical features
 during the illness were no...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573057</comments>
            <pubDate>Thu, 05 Jan 2012 06:52:06 +0100</pubDate>
            <guid isPermaLink="false">5573057</guid>        </item>
        <item>
            <title>Why did we perform a lumbar puncture in a young patient with ischemic stroke?</title>
            <link>http://www.medworm.com/index.php?rid=5573056&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe552543470688275%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-011-6385-2Authors
		R. Geraldes, Stroke Unit, Department of Neurosciences, Santa Maria Hospital, Av. Prof. Egas Moniz, 1649-035 Lisbon, PortugalA. C. Fonseca, Stroke Unit, Department of Neurosciences, Santa Maria Hospital, Av. Prof. Egas Moniz, 1649-035 Lisbon, PortugalP. Canhão, Stroke Unit, Department of Neurosciences, Santa Maria Hospital, Av. Prof. Egas Moniz, 1649-035 Lisbon, PortugalT. P. Melo, Stroke Unit, Department of Neurosciences, Santa Maria Hospital, Av. Prof. Egas Moniz, 1649-035 Lisbon, PortugalJ. M. Ferro, Stroke Unit, Department of Neurosciences, Santa Maria Hospital, Av. Prof. Egas Moniz, 1649-035 Lisbon, Portugal
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573056</comments>
            <pubDate>Thu, 05 Jan 2012 06:52:06 +0100</pubDate>
            <guid isPermaLink="false">5573056</guid>        </item>
        <item>
            <title>Obstructive sleep apnea linked to wake-up strokes</title>
            <link>http://www.medworm.com/index.php?rid=5573058&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3h670178t4133148%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Obstructive sleep apnea (OSA) has been considered as one of the risk factors for ischemic stroke, but the impact of OSA on
 wake-up stroke (WUS) is not well studied. We aimed to determine the relationship between OSA and WUS. We prospectively recruited
 71 patients with mild to moderate ischemic stroke during hospitalization. Patients were classified into WUS and non-WUS. A
 full-night sleep respiratory study was performed between 3 and 14&amp;nbsp;days after stroke onset. Demographic data, sleep respiratory
 data, heart rate variability, stroke risk factors, stroke classification and sleep-related scales were recorded. We compared
 the differences in the variables between the two groups and determined the independent variables associated with WUS. Of the
 71 patients, 26 (...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573058</comments>
            <pubDate>Wed, 04 Jan 2012 06:49:26 +0100</pubDate>
            <guid isPermaLink="false">5573058</guid>        </item>
        <item>
            <title>Glycine receptor antibodies are detected in progressive encephalomyelitis with rigidity and myoclonus (PERM) but not in saccadic oscillations</title>
            <link>http://www.medworm.com/index.php?rid=5573060&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr035207023533556%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Glycine receptor (GlyR) antibodies were recently identified in a few patients with progressive encephalomyelitis with rigidity
 and myoclonus (PERM); none of these patients had antibodies against glutamic acid decarboxylase (GAD). An inhibitory glycinergic
 transmission defect has also been implicated in the mechanism underlying saccadic oscillations, including ocular flutter or
 opsoclonus; GlyR antibodies have not been reported in these patients. The purpose was to determine whether GlyR antibodies
 are found in patients with PERM, ocular flutter syndrome (OFS), and opsoclonus-myoclonus syndrome (OMS). GlyR antibodies were
 first measured in archived sera and CSF from five patients, including one patient with GAD antibody-positive PERM, two patients
 with OFS, and two...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573060</comments>
            <pubDate>Wed, 04 Jan 2012 06:49:23 +0100</pubDate>
            <guid isPermaLink="false">5573060</guid>        </item>
        <item>
            <title>When is neuromyelitis optica diagnosed after disease onset?</title>
            <link>http://www.medworm.com/index.php?rid=5573059&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F221p4w74vml5m242%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To diagnose neuromyelitis optica (NMO), the 2006 NMO diagnostic criteria is commonly used. However, adequate studies about
 the time course of NMO according to the criteria have been lacking. The aim of the study was to identify the interval between
 disease onset and diagnosis of NMO, as well as the clinical characteristics and time course, according to the 2006 NMO diagnostic
 criteria in Japanese patients with NMO. Clinical progression and time course of 43 Japanese patients with NMO who fulfilled
 the 2006 NMO diagnostic criteria with mean disease duration of 14.2&amp;nbsp;years were investigated retrospectively. The initial inflammatory
 event was myelitis in 44.2% (long extensive transverse myelitis [LETM] in 14.3%), optic neuritis in 41.9%, and concurrent
 myelitis a...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573059</comments>
            <pubDate>Wed, 04 Jan 2012 06:49:23 +0100</pubDate>
            <guid isPermaLink="false">5573059</guid>        </item>
        <item>
            <title>Sciatic endometriosis presenting as periodic (catamenial) sciatic radiculopathy</title>
            <link>http://www.medworm.com/index.php?rid=5573061&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fhr36t6g521g62485%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-011-6378-1Authors
		Laura Ghezzi, Department of Neurological Sciences, “Dino Ferrari” Center, Fondazione Cà Granda, IRCCS Ospedale Maggiore Policlinico, University of Milan, Milan, ItalyAndrea Arighi, Department of Neurological Sciences, “Dino Ferrari” Center, Fondazione Cà Granda, IRCCS Ospedale Maggiore Policlinico, University of Milan, Milan, ItalyAnna M. Pietroboni, Department of Neurological Sciences, “Dino Ferrari” Center, Fondazione Cà Granda, IRCCS Ospedale Maggiore Policlinico, University of Milan, Milan, ItalyFrancesca Jacini, Department of Neurological Sciences, “Dino Ferrari” Center, Fondazione Cà Granda, IRCCS Ospedale Maggiore Policlinico, University of Milan, Milan, It...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573061</comments>
            <pubDate>Wed, 04 Jan 2012 06:49:22 +0100</pubDate>
            <guid isPermaLink="false">5573061</guid>        </item>
        <item>
            <title>Detection of clinical and subclinical retinal abnormalities in neurosarcoidosis with optical coherence tomography</title>
            <link>http://www.medworm.com/index.php?rid=5573063&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F055gr566w5065237%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of this work was to determine if neurosarcoidosis (NS) patients exhibit quantitative and/or qualitative in vivo evidence
 of retinal abnormalities on optical coherence tomography (OCT). Retinal imaging was performed using spectral-domain Cirrus
 HD-OCT in 20 NS patients (40 eyes) and 24 age-matched healthy controls (48 eyes). Study participants also underwent magnetic
 resonance imaging of the brain and spine, cerebrospinal fluid (CSF) analysis, and detailed neurological and ophthalmological
 evaluation. Quantitative OCT abnormalities of average macular thickness (AMT), peri-papillary retinal nerve fiber layer (RNFL)
 thickness, or both, were detectable in 60% of NS patients. Of NS patients with ocular symptomatology, 75% demonstrated quantitative
 OCT abnormali...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573063</comments>
            <pubDate>Wed, 04 Jan 2012 06:49:21 +0100</pubDate>
            <guid isPermaLink="false">5573063</guid>        </item>
        <item>
            <title>Inferior vestibular neuritis</title>
            <link>http://www.medworm.com/index.php?rid=5573062&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg5736v546255n3p6%2F</link>
            <description>This study aimed to describe
 the clinical features of VN involving the inferior vestibular labyrinth and its afferents only. Of the 703 patients with a
 diagnosis of VN or labyrinthitis at Seoul National University Bundang Hospital from 2004 to 2010, we retrospectively recruited
 9 patients (6 women, age range 15–75) with a diagnosis of isolated inferior VN. Diagnosis of isolated inferior VN was based
 on torsional downbeating spontaneous nystagmus, abnormal head-impulse test (HIT) for the posterior semicircular canal (PC),
 and abnormal cervical vestibular-evoked myogenic potentials (VEMP) in the presence of normally functioning horizontal and
 anterior semicircular canals, as determined by normal HIT and bithermal caloric tests. All patients presented with acute vertigo
 with nausea, ...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573062</comments>
            <pubDate>Wed, 04 Jan 2012 06:49:21 +0100</pubDate>
            <guid isPermaLink="false">5573062</guid>        </item>
        <item>
            <title>Diagnosis and treatment of upper limb apraxia</title>
            <link>http://www.medworm.com/index.php?rid=5573064&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp32k6396232857j3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Upper limb apraxia, a disorder of higher motor cognition, is a common consequence of left-hemispheric stroke. Contrary to
 common assumption, apraxic deficits not only manifest themselves during clinical testing but also have delirious effects on
 the patients’ everyday life and rehabilitation. Thus, a reliable diagnosis and efficient treatment of upper limb apraxia is
 important to improve the patients’ prognosis after stroke. Nevertheless, to date, upper limb apraxia is still an underdiagnosed
 and ill-treated entity. Based on a systematic literature search, this review summarizes the current tools of diagnosis and
 treatment strategies for upper limb apraxia. It furthermore provides clinicians with graded recommendations. In particular,
 a short screening test fo...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5573064</comments>
            <pubDate>Wed, 04 Jan 2012 06:49:20 +0100</pubDate>
            <guid isPermaLink="false">5573064</guid>        </item>
        <item>
            <title>Pusher syndrome in patients with cerebellar infarctions?</title>
            <link>http://www.medworm.com/index.php?rid=5545625&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fxh17467712x82k06%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-011-6348-7Authors
		Bernhard Baier, Department of Neurology, University of Mainz, Langenbeckstr. 1, 55131 Mainz, GermanyMarianne Dieterich, Department of Neurology, University of Mainz, Langenbeckstr. 1, 55131 Mainz, Germany
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5545625</comments>
            <pubDate>Wed, 21 Dec 2011 20:08:34 +0100</pubDate>
            <guid isPermaLink="false">5545625</guid>        </item>
        <item>
            <title>Posterior reversible encephalopathy syndrome (PRES): electroencephalographic findings and seizure patterns</title>
            <link>http://www.medworm.com/index.php?rid=5545626&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm5pv1167014w655u%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To better describe seizure type, frequency, and electroencephalographic (EEG) findings in posterior reversible encephalopathy
 syndrome (PRES) and correlate these data with clinical and magnetic resonance imaging (MRI) data, we retrospectively assessed
 medical charts and EEG studies of patients with PRES treated between 2004 and 2011. Data collected included patients’ underlying
 pathology, lesion distribution by MRI, seizure type and frequency, EEG pathologic background activity, focal pathology, and
 epileptogenic activity. Thirty-eight of 49 adults with PRES suffered from seizures; 17 underwent EEG and were included in
 the analysis. Perpetuating factors were similar to those reported in the literature. In 15 of 17 patients, MRI showed widespread
 involvement rath...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5545626</comments>
            <pubDate>Wed, 21 Dec 2011 20:08:33 +0100</pubDate>
            <guid isPermaLink="false">5545626</guid>        </item>
        <item>
            <title>Trigger factors for rupture of intracranial aneurysms in relation to patient and aneurysm characteristics</title>
            <link>http://www.medworm.com/index.php?rid=5539257&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu20x35650157365h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Female gender, age above 60&amp;nbsp;years, and an aneurysm larger than 5&amp;nbsp;mm or location on the posterior circulation are associated
 with a higher rupture risk of intracranial aneurysms. We hypothesized that this association is explained by a higher susceptibility
 to (one of) the eight trigger factors that were recently identified. We included 250 patients with aneurysmal subarachnoid
 hemorrhage. We calculated relative risks (RR) with 95% confidence intervals (95% CI) of aneurysmal rupture for trigger factors
 according to sex, age, site, and size of the aneurysms by means of the case-crossover design. None of the triggers except
 for physical exercise differed according to patient and aneurysm characteristics. In the hour after exposure to physical exercise:
 (1) p...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5539257</comments>
            <pubDate>Tue, 20 Dec 2011 16:43:14 +0100</pubDate>
            <guid isPermaLink="false">5539257</guid>        </item>
        <item>
            <title>Passage of an iron bar through the head: 50-year follow-up</title>
            <link>http://www.medworm.com/index.php?rid=5539256&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F43353682xg826227%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-011-6346-9Authors
		B. M. Aji, Cognitive Function Clinic, Walton Centre for Neurology and Neurosurgery, Lower Lane Fazakerley, Liverpool, L9 7LJ UKE. J. Ghadiali, Cognitive Function Clinic, Walton Centre for Neurology and Neurosurgery, Lower Lane Fazakerley, Liverpool, L9 7LJ UKA. Jacob, Cognitive Function Clinic, Walton Centre for Neurology and Neurosurgery, Lower Lane Fazakerley, Liverpool, L9 7LJ UKA. J. Larner, Cognitive Function Clinic, Walton Centre for Neurology and Neurosurgery, Lower Lane Fazakerley, Liverpool, L9 7LJ UK
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5539256</comments>
            <pubDate>Tue, 20 Dec 2011 16:43:14 +0100</pubDate>
            <guid isPermaLink="false">5539256</guid>        </item>
        <item>
            <title>The more things change the more they stay the same: a case report of neurology residency experiences</title>
            <link>http://www.medworm.com/index.php?rid=5539259&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F35x1781241n40101%2F</link>
            <description>This study compared the neurology residency training experience for a single neurology resident at the University of Pennsylvania
 from the years 2002–2005. The prevalence of encounters seen during this residency was compared to the prevalence of neurological
 disorders typically observed by ambulatory neurologists in the United States (US). A total of 1,333 patients were evaluated
 during this residency. Ischemic stroke/transient ischemic accident, epilepsy, metabolic encephalopathy, peripheral neuropathy,
 and multiple sclerosis were the most common neurological disorders observed. The four most common reasons for an outpatient
 visit to a neurologist (i.e., headache/migraine, epilepsy, cerebrovascular disease, and peripheral neuropathy) typically account
 for approximately 49–55% of...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5539259</comments>
            <pubDate>Tue, 20 Dec 2011 16:43:13 +0100</pubDate>
            <guid isPermaLink="false">5539259</guid>        </item>
        <item>
            <title>Screening for balance disorders in mildly affected multiple sclerosis patients</title>
            <link>http://www.medworm.com/index.php?rid=5539258&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbv54l16p4j725n65%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Multiple sclerosis (MS) patients often complain about balance problems when Romberg’s test and tandem gait are normal. The
 aim of the study was to determine if measures of trunk sway taken during a battery of stance and gait tasks could be used
 to detect subclinical balance disorders. We recorded trunk angular sway in the pitch and roll directions from 20 MS patients
 (EDSS 1.4&amp;nbsp;±&amp;nbsp;0.5) and 20 age- and gender-matched healthy controls (HCs), during 12 stance and gait tasks. We filmed 22 subjects
 simultaneously. Two neurologists assessed the videos, deciding whether task performance was pathological. Sway measures were
 significantly different between patients and HCs in eight out of 12 balance tasks. The most significant differences between
 MS patients and...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5539258</comments>
            <pubDate>Tue, 20 Dec 2011 16:43:13 +0100</pubDate>
            <guid isPermaLink="false">5539258</guid>        </item>
        <item>
            <title>Clinical applications of susceptibility weighted imaging in patients with major stroke</title>
            <link>http://www.medworm.com/index.php?rid=5539260&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa367355436210279%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Susceptibility weighted imaging (SWI) is a newly developed magnetic resonance (MR) protocol. Recent studies have found that
 SWI may be useful in the field of cerebrovascular diseases, especially for detecting the presence of prominent veins, microbleeds
 and the susceptibility vessel sign (SVS). Some authors have even suggested that SWI can be used to predict outcome. We conducted
 a prospective study of patients hospitalized with middle cerebral artery territory infarction receiving MRI within 2&amp;nbsp;days
 of stroke onset. The presence of prominent veins, microbleeds and SVS in SWI was analyzed along with hospital characteristics
 of the patients. A total of 44 patients were enrolled. Among the 44 patients, 15 (34.1%) patients showed prominent veins,
 19 (43.2%) showe...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5539260</comments>
            <pubDate>Tue, 20 Dec 2011 16:43:12 +0100</pubDate>
            <guid isPermaLink="false">5539260</guid>        </item>
        <item>
            <title>Clinical predictors of cognitive decline in patients with mild cognitive impairment: the Chongqing aging study</title>
            <link>http://www.medworm.com/index.php?rid=5539261&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F26547q83kj158326%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Mild cognitive impairment (MCI) is considered as the early stage of dementia which currently has no effective treatments.
 Reducing progression of cognitive decline at the MCI stage could be an important strategy for preventing conversion to dementia.
 The goal of this work was to screen for clinical predictors indicating the prognosis of MCI comprehensively; therefor, we
 assumed vascular risk factors (VRFs), carotid stenosis, and white matter changes (WMC) to be independent predictors. A total
 of 257 patients with MCI underwent collection of VRF information, neuropsychological evaluation, computed tomography angiography
 (CTA) to investigate carotid stenosis, and magnetic resonance imaging (MRI) to identify severity of WMC. After a 3-year follow-up
 period, the neuro...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5539261</comments>
            <pubDate>Tue, 20 Dec 2011 16:43:11 +0100</pubDate>
            <guid isPermaLink="false">5539261</guid>        </item>
        <item>
            <title>Intravenous thrombolysis for acute cerebral ischaemia in old stroke patients ≥80 years of age</title>
            <link>http://www.medworm.com/index.php?rid=5539262&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7251x746062u5126%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Despite increasing life expectancy, few data exist on the outcome of elderly stroke patients treated with IV thrombolysis.
 We analyzed the prospectively collected data from the Lille University Hospital stroke unit on patients treated with IV rt-PA
 within 4.5&amp;nbsp;h, comparing patients ≥80&amp;nbsp;years to younger ones. We considered the following outcomes: neurological improvement
 at the acute phase (NIHSS 0 or 1 at 24&amp;nbsp;h, or if the difference between NIHSS at 24&amp;nbsp;h and at baseline was ≥4), occurrence of
 intracerebral haemorrhage, mortality and functional outcome in survivors (favourable if mRS ≤2 or equal to pre-stroke score)
 at 3 months. Predictors of vital and functional outcome were determined using logistic regression analysis. Four hundred patient...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5539262</comments>
            <pubDate>Tue, 20 Dec 2011 06:49:04 +0100</pubDate>
            <guid isPermaLink="false">5539262</guid>        </item>
        <item>
            <title>Assessing the value of spinal cord lesions in predicting development of multiple sclerosis in patients with clinically isolated syndromes</title>
            <link>http://www.medworm.com/index.php?rid=5526956&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Feg68100332261263%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The purpose of this study was to determine the value of spinal cord lesions as a predictive factor for conversion in clinically
 isolated syndrome (CIS) patients. Patients with CIS and without immunomodulatory treatment were prospectively included. Age
 at onset, sex, clinical syndrome at onset, oligoclonal bands, and presence, number and location of lesions on brain and spinal
 MRI were analyzed. Conversion to multiple sclerosis (MS) was the primary endpoint. Cox regression was used to compare outcomes
 between groups. A total of 75 patients were included: 53 (71%) women, mean age at onset 32.7&amp;nbsp;years (SD&amp;nbsp;±&amp;nbsp;7.5), mean follow-up
 time 72.5&amp;nbsp;months (SD&amp;nbsp;±&amp;nbsp;9; range 17–104&amp;nbsp;months). There were 11 (14.6%) patients with one focal spinal cor...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5526956</comments>
            <pubDate>Sat, 17 Dec 2011 06:43:20 +0100</pubDate>
            <guid isPermaLink="false">5526956</guid>        </item>
        <item>
            <title>Clinical and electrophysiological characteristics of neuropathy associated with Tangier disease</title>
            <link>http://www.medworm.com/index.php?rid=5526957&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw204445117036w16%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Tangier disease (TD) (OMIM#205400) is a rare autosomal recessive disorder resulting from mutations in the ABCA1 gene, leading to decreased levels of plasma high-density lipoproteins (HDL). Peripheral neuropathy is a common finding in
 this disease, and may present as relapsing/remitting mono/polyneuropathies or as syringomyelia-like neuropathy. We retrospectively
 analyzed four patients, and report here their clinical, biological, electrophysiological, imaging, and genetic findings.
 Three patients had a typical pseudosyringomyelic neuropathy including facial diplegia, but asymmetrical onset was observed
 in one patient who had first been misdiagnosed with Lewis–Sumner syndrome. Electrophysiological pattern was heterogeneous,
 showing both signs of demyelination and a...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5526957</comments>
            <pubDate>Sat, 17 Dec 2011 06:43:19 +0100</pubDate>
            <guid isPermaLink="false">5526957</guid>        </item>
        <item>
            <title>Impaired oculomotor function in a community-based patient population with newly diagnosed idiopathic parkinsonism</title>
            <link>http://www.medworm.com/index.php?rid=5516348&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk288165173337478%2F</link>
            <description>We examined the oculomotor function in a population-based
 incidence cohort with newly diagnosed idiopathic parkinsonism and 38 controls. We examined 135 patients with parkinsonism
 105 PD, 11 progressive supranuclear palsy (PSP), and 19 multiple system atrophy with predominant parkinsonism (MSA-P)] within
 3&amp;nbsp;months of their first visit to our clinic and before initiation of dopaminergic medication. The oculomotor measurements
 were repeated after 12&amp;nbsp;months. The clinical diagnosis was that of the latest clinical follow-up (median follow-up was 3&amp;nbsp;years).
 All patients were examined with 123I-N-(omega)-fluoropropyl-2-β-carbomethoxy-3-β-(4-iodophenyl) nortropane single-photon emission computed tomography (FP-CIT SPECT),
 and only patients with pathological uptake of the ligan...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5516348</comments>
            <pubDate>Fri, 16 Dec 2011 06:54:03 +0100</pubDate>
            <guid isPermaLink="false">5516348</guid>        </item>
        <item>
            <title>Transcranial magnetic stimulation in mild to severe hemiparesis early after stroke: a proof of principle and novel approach to improve motor function</title>
            <link>http://www.medworm.com/index.php?rid=5516347&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F427412375113202h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Low-frequency repetitive transcranial magnetic stimulation (rTMS) of the unaffected hemisphere can enhance function of the
 paretic hand in patients with mild motor impairment. Effects of low-frequency rTMS to the contralesional motor cortex at an
 early stage of mild to severe hemiparesis after stroke are unknown. In this pilot, randomized, double-blind clinical trial
 we compared the effects of low-frequency rTMS or sham rTMS as add-on therapies to outpatient customary rehabilitation, in
 30 patients within 5–45&amp;nbsp;days after ischemic stroke, and mild to severe hand paresis. The primary feasibility outcome was compliance
 with the interventions. The primary safety outcome was the proportion of intervention-related adverse events. Performance
 of the paretic hand i...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5516347</comments>
            <pubDate>Fri, 16 Dec 2011 06:54:03 +0100</pubDate>
            <guid isPermaLink="false">5516347</guid>        </item>
        <item>
            <title>New hands at the helm</title>
            <link>http://www.medworm.com/index.php?rid=5516349&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv40116j2v2l61gj8%2F</link>
            <description>Content Type Journal ArticleCategory EditorialPages 1-3DOI 10.1007/s00415-011-6358-5Authors
		Roger A. Barker, Cambridge Centre for Brain Repair, University of Cambridge, The E.D. Adrian Building, Forvie Site, Robinson Way, Cambridge, CB2 2PY UK
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5516349</comments>
            <pubDate>Thu, 15 Dec 2011 16:51:50 +0100</pubDate>
            <guid isPermaLink="false">5516349</guid>        </item>
        <item>
            <title>Atypical manifestations in Brazilian patients with neuro-Behçet’s disease</title>
            <link>http://www.medworm.com/index.php?rid=5516350&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F07386362n7371u64%2F</link>
            <description>We describe clinical and radiological features of 36 Brazilian patients of mixed ethnicity with neuro-Behçet’s
 disease (NBD). Medical records of 178 BD patients were reviewed and 36 (20%) NBD patients were identified. Twenty-one NBD
 patients (58.3%) were female and 27 (75%) presented with parenchymal manifestations. Brainstem involvement was the most common
 neurologic syndrome (41.7%). Seizures (27.8%), isolated aseptic meningitis (16.7%), optic neuropathy (ON) (16.7%), cerebral
 venous thrombosis (CVT) (8.3%), peripheral neuropathy (2.8%), and spinal cord involvement (5.6%) were other neurologic manifestations
 observed among Brazilian NBD patients. Eighteen (50%) had at least one relapse, and isolated aseptic meningitis was the most
 common relapsing manifestation. No significant d...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5516350</comments>
            <pubDate>Wed, 14 Dec 2011 16:42:41 +0100</pubDate>
            <guid isPermaLink="false">5516350</guid>        </item>
        <item>
            <title>Anti-voltage-gated potassium channel Kv1.4 antibodies in myasthenia gravis</title>
            <link>http://www.medworm.com/index.php?rid=5516351&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq8t5162647830666%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Myasthenia gravis (MG) is an autoimmune disease characterized by skeletal muscle weakness mainly caused by acetylcholine receptor
 antibodies. MG can be divided into generalized and ocular, and into early-onset (&amp;lt;50&amp;nbsp;years of age) and late-onset (≥50&amp;nbsp;years
 of age). Anti-Kv1.4 antibodies targeting α-subunits (Kv1.4) of the voltage-gated potassium K+ channel occurs frequently among patients with severe MG, accounting for 18% of a Japanese MG population. The aim of this
 study was to characterize the clinical features and serological associations of anti-Kv1.4 antibodies in a Caucasian MG population
 with mild and localized MG. Serum samples from 129 Caucasian MG patients with mainly ocular symptoms were tested for the presence
 of anti-Kv1.4 antibodies and...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5516351</comments>
            <pubDate>Tue, 13 Dec 2011 17:05:58 +0100</pubDate>
            <guid isPermaLink="false">5516351</guid>        </item>
        <item>
            <title>Erratum to: CHA2DS2-VASc score and prognosis in ischemic strokes with atrial fibrillation</title>
            <link>http://www.medworm.com/index.php?rid=5506736&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fgp12429607076236%2F</link>
            <description>Content Type Journal ArticleCategory ErratumPages 1-1DOI 10.1007/s00415-011-6351-zAuthors
		Eva Giralt-Steinhauer, Neurology Department, Neurovascular Research Group, IMIM-Hospital del Mar, Universitat Autònoma de Barcelona, Barcelona, SpainElisa Cuadrado-Godia, Neurology Department, Neurovascular Research Group, IMIM-Hospital del Mar, Universitat Autònoma de Barcelona, Barcelona, SpainÁngel Ois, Neurology Department, Neurovascular Research Group, IMIM-Hospital del Mar, Universitat Autònoma de Barcelona, Barcelona, SpainJordi Jiménez-Conde, Neurology Department, Neurovascular Research Group, IMIM-Hospital del Mar, Universitat Autònoma de Barcelona, Barcelona, SpainAna Rodríguez-Campello, Neurology Department, Neurovascular Research Group, IMIM-Hospital del Mar, Universitat Autòno...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506736</comments>
            <pubDate>Mon, 12 Dec 2011 17:13:38 +0100</pubDate>
            <guid isPermaLink="false">5506736</guid>        </item>
        <item>
            <title>Effect of natalizumab on clinical and radiological disease activity in a French cohort of patients with relapsing-remitting multiple sclerosis</title>
            <link>http://www.medworm.com/index.php?rid=5506735&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F120246714ph31728%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;“Disease activity free” in relapsing-remitting multiple sclerosis (RRMS) is a new concept introduced by the results of the
 AFFIRM study. Our objective was to analyze the clinical and radiological efficacy of natalizumab treatment in actual clinical
 practice and compare it with the post hoc analysis of the AFFIRM study. All patients with RRMS who began treatment with natalizumab
 at our two French MS centres between April 2007 and May 2008 were included and followed-up for at least 2&amp;nbsp;years. No measurable
 disease activity (“disease activity free”) was defined as no activity on clinical measures (no relapses and no sustained disability
 progression) and radiological measures (no gadolinium-enhancing lesions and no new T2-hyperintense lesions on cerebral MRI...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506735</comments>
            <pubDate>Mon, 12 Dec 2011 17:13:38 +0100</pubDate>
            <guid isPermaLink="false">5506735</guid>        </item>
        <item>
            <title>Decreased microglial activation in MS patients treated with glatiramer acetate</title>
            <link>http://www.medworm.com/index.php?rid=5495942&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp83m153076482550%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Activated microglia are thought to be an important contributor to tissue damage in multiple sclerosis (MS). The level of microglial
 activation can be measured non-invasively using [11C]-R-PK11195, a radiopharmaceutical for positron emission tomography (PET). Prior studies have identified abnormalities in the
 level of [11C]-R-PK11195 uptake in patients with MS, but treatment effects have not been evaluated. Nine previously untreated relapsing-remitting
 MS patients underwent PET and magnetic resonance imaging of the brain at baseline and after 1&amp;nbsp;year of treatment with glatiramer
 acetate. Parametric maps of [11C]-R-PK11195 uptake were obtained for baseline and post-treatment PET scans, and the change in [11C]-R-PK11195 uptake pre- to post-treatment was evaluated a...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5495942</comments>
            <pubDate>Thu, 08 Dec 2011 18:11:56 +0100</pubDate>
            <guid isPermaLink="false">5495942</guid>        </item>
        <item>
            <title>The association of systemic lupus erythematosus and myasthenia gravis: a series of 17 cases, with a special focus on hydroxychloroquine use and a review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=5488493&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy7rj342377rr4h08%2F</link>
            <description>In conclusion, the clinical pattern of patients with SLE and MG seems to be characterized by a less
 severe course of SLE and higher frequency of antiphospholipid antibodies. Hydroxychloroquine treatment appears to be safe
 in this setting.
 
 
	Content Type Journal ArticleCategory Original CommunicationPages 1-8DOI 10.1007/s00415-011-6335-zAuthors
		M. Jallouli, Service de Médecine Interne, Centre de référence national pour le Lupus Systémique et le syndrome des Antiphospholipides, Centre Hospitalier Universitaire Pitié-Salpêtrière, Université Paris 6, AP-HP, 47-83 Boulevard de l’Hôpital, 75651 Paris Cedex 13, FranceD. Saadoun, Service de Médecine Interne, Centre de référence national pour le Lupus Systémique et le syndrome des Antiphospholipides, Centre Hospitalier Univers...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488493</comments>
            <pubDate>Wed, 07 Dec 2011 17:33:23 +0100</pubDate>
            <guid isPermaLink="false">5488493</guid>        </item>
        <item>
            <title>Effects of dual tasking on the postural performance of people with and without multiple sclerosis: a pilot study</title>
            <link>http://www.medworm.com/index.php?rid=5488495&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj1485152x1t67k1n%2F</link>
            <description>This study examined the effects of MS
 and of dual tasking on postural performance, and explored associations among dual-task postural performance, cognitive capacity,
 fear of falling, and fatigue. Thirteen subjects with MS (Expanded Disability Status Scale: 0–4.5) and 13 matched subjects
 without MS performed three tasks of standing postural control, with and without dual tasking amid an auditory Stroop task:
 (1) step initiation, (2) forward leaning to the limits of stability, and (3) postural responses to rotations of the support
 surface. Two-factor general linear models were used to evaluate differences between the groups (with or without MS) and two
 conditions (single or dual tasking) for each postural task. During step initiation, dual tasking significantly delayed the
 onset of...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488495</comments>
            <pubDate>Wed, 07 Dec 2011 16:44:27 +0100</pubDate>
            <guid isPermaLink="false">5488495</guid>        </item>
        <item>
            <title>Drummer’s lower limb dystonia</title>
            <link>http://www.medworm.com/index.php?rid=5488494&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3516145361755778%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-011-6324-2Authors
		Jaume Rosset-Llobet, Institut de Fisiologia i Medicina de l’Art-Terrassa, Ctra. de Montcada 668, 08227 Terrassa (Barcelona), SpainSílvia Fàbregas-Molas, Institut de Fisiologia i Medicina de l’Art-Terrassa, Ctra. de Montcada 668, 08227 Terrassa (Barcelona), SpainÁlvaro Pascual-Leone, Berenson-Allen Center for Noninvasive Brain Stimulation, Cognitive Neurology Unit, Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488494</comments>
            <pubDate>Wed, 07 Dec 2011 16:44:27 +0100</pubDate>
            <guid isPermaLink="false">5488494</guid>        </item>
        <item>
            <title>Biomarkers demonstrate increased consumption, but not abuse, of ethanol in essential tremor</title>
            <link>http://www.medworm.com/index.php?rid=5488497&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F667u336lx013n7w6%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ethanol is known to improve tremor in a proportion of patients with essential tremor. Increased incidence of alcoholism has
 been suspected in essential tremor patients; however, no objective evaluation has been performed using laboratory markers
 to date. Data on alcohol intake in the last 30&amp;nbsp;days were acquired in 95 essential tremor patients and 35 healthy controls.
 Blood and urine markers related to alcohol metabolism and liver function were evaluated. Self-reported alcohol intake and
 biomarker levels were higher in essential tremor, but the difference was only significant for carbohydrate-deficient transferrin.
 None of the subjects presented with laboratory parameters reflecting chronic alcohol abuse. Our data do not reflect a higher
 incidence of alcoholism...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488497</comments>
            <pubDate>Tue, 06 Dec 2011 19:09:38 +0100</pubDate>
            <guid isPermaLink="false">5488497</guid>        </item>
        <item>
            <title>Comparison of the new ASCO classification with the TOAST classification in a population with acute ischemic stroke</title>
            <link>http://www.medworm.com/index.php?rid=5488496&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn56wp11415882512%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Precise analysis of stroke subtypes is important for clinical treatment decisions, the prognostic evaluation of patients,
 as well as defining stroke populations in clinical studies. The TOAST classification is the most widely used and approved
 form for etiologic subtyping. Increasing knowledge about stroke mechanisms and the introduction of new diagnostic techniques
 have supported the promotion of the new ASCO phenotypic classification, which aims to characterize patients using different
 grades of evidence for stroke subtypes. We prospectively assigned 103 consecutive patients from our stroke center for subtype
 classification using ASCO and TOAST. Clinical features and complementary investigations were recorded according to our standardized
 acute stroke care proto...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488496</comments>
            <pubDate>Tue, 06 Dec 2011 19:09:38 +0100</pubDate>
            <guid isPermaLink="false">5488496</guid>        </item>
        <item>
            <title>Guillain–Barré syndrome associated with normal or exaggerated tendon reflexes</title>
            <link>http://www.medworm.com/index.php?rid=5488499&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fuw71405563320481%2F</link>
            <description>This study demonstrated that DTRs could be normal or hyperexcitable during the entire clinical course in approximately
 10% of GBS patients. This possibility should be added in the diagnostic criteria for GBS to avoid delays in diagnosis and
 effective treatment to these patients.
 
 
	Content Type Journal ArticleCategory Original CommunicationPages 1-10DOI 10.1007/s00415-011-6330-4Authors
		Nobuhiro Yuki, Departments of Microbiology and Medicine, National University of Singapore, Block MD4A, Level 5, 5 Science Drive 2, Singapore, 117597 SingaporeNorito Kokubun, Department of Neurology, Dokkyo Medical University, Tochigi, JapanSatoshi Kuwabara, Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, JapanYukari Sekiguchi, Department of Neurology, Graduate School of M...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488499</comments>
            <pubDate>Tue, 06 Dec 2011 07:00:58 +0100</pubDate>
            <guid isPermaLink="false">5488499</guid>        </item>
        <item>
            <title>Failure of long-term subthalamic nucleus stimulation corrected by additional pallidal stimulation in a patient with Parkinson’s disease</title>
            <link>http://www.medworm.com/index.php?rid=5488498&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4802431745882r42%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-3DOI 10.1007/s00415-011-6331-3Authors
		Niels Allert, Neurological Rehabilitation Center Godeshoehe, Waldstrasse 2-10, 53177 Bonn, GermanyAlfons Schnitzler, Department of Neurology-Movement Disorders and Neuromodulation, Heinrich-Heine-University Duesseldorf, Moorenstrasse 5, 40225 Duesseldorf, GermanyVolker Sturm, Department of Stereotaxy and Functional Neurosurgery, University Hospital Cologne, Joseph-Stelzmann-Strasse 9, 50924 Cologne, GermanyMohammad Maarouf, Department of Stereotaxy and Functional Neurosurgery, University Hospital Cologne, Joseph-Stelzmann-Strasse 9, 50924 Cologne, Germany
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488498</comments>
            <pubDate>Tue, 06 Dec 2011 07:00:58 +0100</pubDate>
            <guid isPermaLink="false">5488498</guid>        </item>
        <item>
            <title>Deficient sustained attention to response task and P300 characteristics in early Huntington’s disease</title>
            <link>http://www.medworm.com/index.php?rid=5488500&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc7824630157072k3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Evidence for the extent and nature of attentional impairment in premanifest and manifest Huntington’s disease (HD) is inconsistent.
 Understanding such impairments may help to better understand early functional changes in HD and could have consequences concerning
 care for HD patients. We investigated attentional control in both early and premanifest HD. We studied 17 early HD subjects
 (mean age: 51 years), 12 premanifest HD subjects (mean age: 43 years), and 15 healthy controls (mean age: 51 years), using
 the sustained attention to response task (SART), a simple Go/No-go test reflecting attentional and inhibitory processes through
 reaction time (RT) and error rates. Simultaneously recorded EEG yielded P300 amplitudes and latencies. The early HD group
 made more Go...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488500</comments>
            <pubDate>Mon, 05 Dec 2011 17:36:24 +0100</pubDate>
            <guid isPermaLink="false">5488500</guid>        </item>
        <item>
            <title>PINK1: pumps, paraesthesia, punding and psychosis</title>
            <link>http://www.medworm.com/index.php?rid=5470270&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F207366x730602081%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-011-6327-zAuthors
		Dominic C. Paviour, Department of Neurology, Atkinson Morley Wing, St George’s Hospital NHS Trust, London, SW17 OQT UKMarie-Helene Marion, Department of Neurology, Atkinson Morley Wing, St George’s Hospital NHS Trust, London, SW17 OQT UK
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5470270</comments>
            <pubDate>Wed, 30 Nov 2011 04:39:35 +0100</pubDate>
            <guid isPermaLink="false">5470270</guid>        </item>
        <item>
            <title>Exacerbation of dementia after the earthquake and tsunami in Japan</title>
            <link>http://www.medworm.com/index.php?rid=5470271&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F936117p12844387u%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-1DOI 10.1007/s00415-011-6329-xAuthors
		Katsutoshi Furukawa, Department of Geriatrics and Gerontology, Division of Brain Sciences, Institute of Development, Aging and Cancer, Tohoku University, 4-1 Seiryo-cho Aobaku, Sendai, 980-8575 JapanMari Ootsuki, Department of Geriatrics and Gerontology, Division of Brain Sciences, Institute of Development, Aging and Cancer, Tohoku University, 4-1 Seiryo-cho Aobaku, Sendai, 980-8575 JapanManabu Kodama, Division of Psychiatry, Kodama Hospital, Ishinomaki, JapanHiroyuki Arai, Department of Geriatrics and Gerontology, Division of Brain Sciences, Institute of Development, Aging and Cancer, Tohoku University, 4-1 Seiryo-cho Aobaku, Sendai, 980-8575 Japan
	

	
		Journal Journal of Neurolog...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5470271</comments>
            <pubDate>Wed, 30 Nov 2011 04:39:34 +0100</pubDate>
            <guid isPermaLink="false">5470271</guid>        </item>
        <item>
            <title>Concerns about studies investigating new anticoagulant drugs for stroke prevention in atrial fibrillation</title>
            <link>http://www.medworm.com/index.php?rid=5470272&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6180l23j7j56h222%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-011-6328-yAuthors
		Claudia Stöllberger, Second Medical Department, Krankenanstalt Rudolfstiftung, Juchgasse 25, 1030 Vienna, AustriaJosef Finsterer, Second Medical Department, Krankenanstalt Rudolfstiftung, Juchgasse 25, 1030 Vienna, Austria
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5470272</comments>
            <pubDate>Tue, 29 Nov 2011 22:21:59 +0100</pubDate>
            <guid isPermaLink="false">5470272</guid>        </item>
        <item>
            <title>Chronic immune sensory polyradiculopathy with cranial and peripheral nerve involvement</title>
            <link>http://www.medworm.com/index.php?rid=5470273&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F53877j45261n856n%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-3DOI 10.1007/s00415-011-6326-0Authors
		S. Anand Trip, MRC Centre for Neuromuscular Diseases, Department of Molecular Neurosciences, UCL Institute of Neurology, Queen Square, London, WC1N 3BG UKTabish Saifee, MRC Centre for Neuromuscular Diseases, Department of Molecular Neurosciences, UCL Institute of Neurology, Queen Square, London, WC1N 3BG UKWill Honan, Department of Neurology, Royal Devon and Exeter Hospital, Exeter, UKHoskote Chandrashekar, Lysholm Department of Neuroradiology, National Hospital for Neurology and Neurosurgery, Queen Square, London, UKMichael P. Lunn, MRC Centre for Neuromuscular Diseases, Department of Molecular Neurosciences, UCL Institute of Neurology, Queen Square, London, WC1N 3BG UKTarek Yousry,...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5470273</comments>
            <pubDate>Tue, 29 Nov 2011 22:21:58 +0100</pubDate>
            <guid isPermaLink="false">5470273</guid>        </item>
        <item>
            <title>Short-term stability of T1 and T2 relaxation measures in multiple sclerosis normal appearing white matter</title>
            <link>http://www.medworm.com/index.php?rid=5450272&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj5127ht704l0675q%2F</link>
            <description>We examined the short-term evolution of MWF, GMT2 and T
 1 in MS NAWM based on monthly scanning over 6&amp;nbsp;months in 18 relapsing remitting (RR) MS subjects. Histogram metrics demonstrated
 short-term stability of T
 1, MWF and remitting (RR) MS subjects. We observed no change in MWF, GMT2 or T
 1 histogram metrics in NAWM in RRMS over the course of 6&amp;nbsp;months. Longer follow-up periods may be required to establish demonstrable
 changes in NAWM based on of MWF, GMT2 and T
 1 metrics.
 
 
	Content Type Journal ArticleCategory Original CommunicationPages 1-8DOI 10.1007/s00415-011-6318-0Authors
		Alice L. W. Liang, Department of Physics and Astronomy, University of British Columbia, Vancouver, BC, CanadaIrene M. Vavasour, Department of Radiology, University of British Columbia, Vancouver, ...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5450272</comments>
            <pubDate>Fri, 25 Nov 2011 17:43:08 +0100</pubDate>
            <guid isPermaLink="false">5450272</guid>        </item>
        <item>
            <title>Erratum to: Serum levels of cytokines and C-reactive protein in acute ischemic stroke patients, and their relationship to stroke lateralization, type, and infarct volume</title>
            <link>http://www.medworm.com/index.php?rid=5450271&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkq542u428g8p0640%2F</link>
            <description>Content Type Journal ArticleCategory ErratumPages 1-1DOI 10.1007/s00415-011-6333-1Authors
		Heidi Ormstad, Vestre Viken Hospital Trust, Bærum sykehus, Postbox 83, 1309 Rud, NorwayHans Christian Dalsbotten Aass, The R &amp; D Group, Department of Medical Biochemistry, Oslo University Hospital, Ullevål, Oslo, NorwayNiels Lund-Sørensen, Department of Radiology, Vestre Viken Hospital Trust, Buskerud, NorwayKarl-Friedrich Amthor, Department of Neurology, Vestre Viken Hospital Trust, Buskerud, NorwayLeif Sandvik, Section of Biostatistics, Oslo University Hospital, Ullevål, Oslo, Norway
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5450271</comments>
            <pubDate>Fri, 25 Nov 2011 17:43:08 +0100</pubDate>
            <guid isPermaLink="false">5450271</guid>        </item>
        <item>
            <title>Erratum to: Serum cytokine and glucose levels as predictors of poststroke fatigue in acute ischemic stroke patients</title>
            <link>http://www.medworm.com/index.php?rid=5450273&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Frj426317318620k1%2F</link>
            <description>Content Type Journal ArticleCategory ErratumPages 1-1DOI 10.1007/s00415-011-6332-2Authors
		Heidi Ormstad, Vestre Viken Hospital Trust, Ringerike, Servicebox 13, 3530 Hønefoss, NorwayHans Christian Dalsbotten Aass, The R &amp; D Group, Department of Medical Biochemistry, Oslo University Hospital, Ullevål, Oslo, NorwayKarl-Friedrich Amthor, Department of Neurology, Vestre Viken Hospital Trust, Buskerud, NorwayNiels Lund-Sørensen, Department of Radiology, Vestre Viken Hospital Trust, Buskerud, NorwayLeiv Sandvik, Section of Biostatistics, Oslo University Hospital, Ullevål, Oslo, Norway
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5450273</comments>
            <pubDate>Fri, 25 Nov 2011 17:43:07 +0100</pubDate>
            <guid isPermaLink="false">5450273</guid>        </item>
        <item>
            <title>Decompressive hemicraniectomy in severe cerebral venous thrombosis: a prospective case series</title>
            <link>http://www.medworm.com/index.php?rid=5450274&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg834525782t47626%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Small retrospective case series suggest that decompressive hemicraniectomy can be life saving in patients with cerebral venous
 thrombosis (CVT) and impending brain herniation. Prospective studies of consecutive cases are lacking. Thus, a single centre,
 prospective study was performed. In 2006 we adapted our protocol for CVT treatment to perform acute decompressive hemicraniectomy
 in patients with impending herniation, in whom the prognosis with conservative treatment was considered infaust. We included
 all consecutive patients with CVT between 2006 and 2010 who underwent hemicraniectomy. Outcome was assessed at 12&amp;nbsp;months with
 the modified Rankin Scale (mRS). Ten patients (8 women) with a median age of 41&amp;nbsp;years (range 26–52&amp;nbsp;years) were included. Bef...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5450274</comments>
            <pubDate>Fri, 25 Nov 2011 17:43:05 +0100</pubDate>
            <guid isPermaLink="false">5450274</guid>        </item>
        <item>
            <title>Visual dependence and BPPV</title>
            <link>http://www.medworm.com/index.php?rid=5450275&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk17230lr723truh2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The increased visual dependence noted in some vestibular patients may be secondary to their vertigo. We examine whether a
 single, brief vertigo attack, such as in benign paroxysmal positional vertigo (BPPV), modifies visual dependency. Visual dependency
 was measured before and after the Hallpike manoeuvre with (a) the Rod and Frame and the Rod and Disc techniques whilst seated
 and (b) the postural sway induced by visual roll-motion stimulation. Three subject groups were studied: 20 patients with BPPV
 (history and positive Hallpike manoeuvre; PosH group), 20 control patients (history of BPPV but negative Hallpike manoeuvre;
 NegH group) and 20 normal controls. Our findings show that while both patient groups showed enhanced visual dependency, the
 PosH and the normal...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5450275</comments>
            <pubDate>Thu, 24 Nov 2011 06:50:41 +0100</pubDate>
            <guid isPermaLink="false">5450275</guid>        </item>
        <item>
            <title>Progressive neurological deficits in multiple myeloma: meningeal myelomatosis without MRI abnormalities</title>
            <link>http://www.medworm.com/index.php?rid=5450276&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fqg62g53r63657635%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-3DOI 10.1007/s00415-011-6313-5Authors
		S. van Ginkel, Department of Neurology, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The NetherlandsT. J. Snijders, Department of Neurology (G03.228), University Medical Center Utrecht, P.O. Box 85500, 3508 GA Utrecht, The NetherlandsN. W. C. J. van de Donk, Department of Haematology, University Medical Center Utrecht, Utrecht, The NetherlandsC. J. M. Klijn, Department of Neurology, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The NetherlandsM. L. D. Broekman, Department of Neurosurgery, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands
	

	
		Journal Jou...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5450276</comments>
            <pubDate>Wed, 23 Nov 2011 16:32:33 +0100</pubDate>
            <guid isPermaLink="false">5450276</guid>        </item>
        <item>
            <title>Impact of low mini-mental status on health outcome up to 5 years after stroke: the Erlangen Stroke Project</title>
            <link>http://www.medworm.com/index.php?rid=5450277&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8r017643621q1t77%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cognitive deficits are frequent stroke sequelae. Data from population-based stroke cohorts on the impact of cognitive deficits
 on long-term outcome are scarce. The purpose of this study was to investigate the impact of low mini-mental status on health
 outcome up to 5&amp;nbsp;years after first-ever stroke. Data were collected from the Erlangen Stroke Project, a population-based stroke
 registry covering a source population of 103,000 inhabitants. The Mini-Mental State Examination (MMSE) was used to assess
 global cognitive function. Health outcome included limitations in instrumental activities of daily living (IADL, Frenchay
 Activities Index), low independence in activities of daily living (ADL, Barthel Index), depressive symptoms (Zung Self Rating
 Depression Scale), a...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5450277</comments>
            <pubDate>Tue, 22 Nov 2011 17:57:16 +0100</pubDate>
            <guid isPermaLink="false">5450277</guid>        </item>
        <item>
            <title>Magnetic resonance imaging of lower limb musculature in acute motor axonal neuropathy</title>
            <link>http://www.medworm.com/index.php?rid=5450278&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fynq42w76jkg7040h%2F</link>
            <description>This report presents an
 acute motor axonal neuropathy (AMAN) patient in whom, over 2&amp;nbsp;years, serial clinical-electrophysiological evaluation and MRI
 examination of lower limb musculature were performed. A 74-year-old patient was admitted with a 24-h history of ascending
 weakness culminating a few days later in flaccid and areflexic tetraplegia, which was followed by progressive improvement
 except for severe residual paresis of foot flexors/extensors. Electrophysiological studies showed motor nerve conduction abnormalities
 characteristic of AMAN, and profuse signs of active denervation in foot and lower leg muscles, and to a much lesser degree
 in the thigh muscles. On MRI, T2- and T2-fat suppressed (T2FS) images showed an early (up to month&amp;nbsp;2 after onset) and subtle
 hypersig...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5450278</comments>
            <pubDate>Tue, 22 Nov 2011 17:57:15 +0100</pubDate>
            <guid isPermaLink="false">5450278</guid>        </item>
        <item>
            <title>Transient floating thrombus of the internal carotid artery associated with the JAK2V617F mutation</title>
            <link>http://www.medworm.com/index.php?rid=5450281&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F632l802862713h2t%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-011-6320-6Authors
		Patricia Martinez-Sanchez, Department of Neurology and Stroke Center, IdiPAZ Research Institute, La Paz University Hospital, Autonoma University of Madrid, Paseo de la Castellana 261, 28046 Madrid, SpainRubén Cazorla-García, Department of Neurology and Stroke Center, IdiPAZ Research Institute, La Paz University Hospital, Autonoma University of Madrid, Paseo de la Castellana 261, 28046 Madrid, SpainJosmarlin Medina-Báez, Department of Neurology and Stroke Center, IdiPAZ Research Institute, La Paz University Hospital, Autonoma University of Madrid, Paseo de la Castellana 261, 28046 Madrid, SpainBlanca Fuentes, Department of Neurology and Stroke Center, IdiPAZ Research Institute, La ...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5450281</comments>
            <pubDate>Tue, 22 Nov 2011 17:57:13 +0100</pubDate>
            <guid isPermaLink="false">5450281</guid>        </item>
        <item>
            <title>Associated autoimmune diseases in patients with multifocal motor neuropathy and their family members</title>
            <link>http://www.medworm.com/index.php?rid=5450280&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn32858260p8v344k%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Multifocal motor neuropathy (MMN) is a rare immune-mediated disorder and is characterized by male predominance, the presence
 of serum anti-GM1 IgM antibodies in up to half of all patients, responsiveness to intravenous immunoglobulins (IVIg) and an
 increased frequency of HLA type HLA-DRB1*15. The aim of this study was to assess whether the frequency of autoimmune diseases
 (AID) is increased in patients with MMN and their first-degree family members, since this would indicate that MMN shares pathogenic
 mechanisms with other AID. We conducted a case–control study using questionnaires to evaluate the prevalence of AID in MMN
 and controls, and their first-degree relatives. Questionnaires from 81 MMN patients (417 first-degree relatives) and 438 controls
 (2,377 first...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5450280</comments>
            <pubDate>Tue, 22 Nov 2011 17:57:13 +0100</pubDate>
            <guid isPermaLink="false">5450280</guid>        </item>
        <item>
            <title>Central nervous system (CNS) tumor trends in children in a western Canadian province: a population-based 22-year retrospective study</title>
            <link>http://www.medworm.com/index.php?rid=5450279&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff488792454x33774%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In Canada, CNS tumors accounted for nearly 22% of the new childhood cancer diagnoses during 1995–2000 in the ≤15&amp;nbsp;year age
 group. The study’s objective was to describe children and youth (age &amp;lt;20&amp;nbsp;years) diagnosed with CNS tumors in Alberta, Canada
 during a 22-year period using population-based data. The Alberta Cancer registry was used to extract information, including
 sex, age and geography, on all CNS (ICCC-3 III) tumor diagnoses during April 1, 1982, and March 31, 2004. Analyses included
 population summaries and rates. During 22 fiscal years, 568 Alberta children were diagnosed with CNS tumors and nearly 82%
 of the cases were malignant (461). The majority of cases were male (322, 57%) and the median age at diagnosis was 8&amp;nbsp;years.
 The crude...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5450279</comments>
            <pubDate>Tue, 22 Nov 2011 17:57:13 +0100</pubDate>
            <guid isPermaLink="false">5450279</guid>        </item>
        <item>
            <title>Low depressive symptoms in acute spinal cord injury compared to other neurological disorders</title>
            <link>http://www.medworm.com/index.php?rid=5432872&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe595472r704u8l57%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of the study was to reveal the incidence and time course of depressive symptoms following acute spinal cord injury
 (SCI) in relation to clinical outcomes for comparison to other neurological disorders with severe impairment. In patients
 with acute traumatic SCI (n&amp;nbsp;=&amp;nbsp;130), combined follow up assessments of neurological and functional outcomes, pain and patient-rated affective factors
 (e.g. mood, anxiety) were prospectively (1, 3, 6, 12&amp;nbsp;months after injury) collected during rehabilitation and follow up in
 out-patient clinics. We related these to the severity of depressive symptoms (no, mild, moderate and severe) based on the
 Beck Depression Inventory (BDI) scores. The mean 65% of patients showed no depressive symptoms and 30% mild depressive sy...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5432872</comments>
            <pubDate>Fri, 18 Nov 2011 07:00:38 +0100</pubDate>
            <guid isPermaLink="false">5432872</guid>        </item>
        <item>
            <title>The pulvinar sign in Fabry patients: the first report in female patients</title>
            <link>http://www.medworm.com/index.php?rid=5432873&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fmg104736mt1987u4%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-011-6305-5Authors
		Alessandro P. Burlina, Neurological Unit, San Bassiano Hospital, Via dei Lotti 40, 36061 Bassano del Grappa, ItalyJuan Politei, Department of Neurology, Juan Fernandez Hospital, Buenos Aires, ArgentinaSarah Cinque, Department of Dermatology, Cosme Argerich Hospital, Buenos Aires, ArgentinaAndrea Soliani, Department of Dermatology, Cosme Argerich Hospital, Buenos Aires, ArgentinaRobert Y. Carlier, Department of Radiology, Raymond Poincaré Hospital, Garches, FranceDominique P. Germain, Division of Medical Genetics, Raymond Poincaré Hospital, University of Versailles-Saint Quentin en Yvelines, Garches, FranceRenzo Manara, Neuroradiology Unit, University Hospital, Padova, Italy
	

	
		...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5432873</comments>
            <pubDate>Fri, 18 Nov 2011 07:00:37 +0100</pubDate>
            <guid isPermaLink="false">5432873</guid>        </item>
        <item>
            <title>Understanding the impact of deep brain stimulation on ambulatory activity in advanced Parkinson’s disease</title>
            <link>http://www.medworm.com/index.php?rid=5423718&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F74nn5n3260830034%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Whilst deep brain stimulation of the subthalamic nucleus (DBS-STN) improves the motor symptoms of Parkinson’s disease (PD),
 its effect on daily activity is unknown. We aimed to quantify changes in ambulatory activity following DBS-STN in advanced
 PD using novel accelerometry based measures that describe changes to the volume and pattern of walking. Seventeen participants
 with advanced PD were measured over a 7-day period using an activPAL
 ™ activity monitor. Data were collected 6&amp;nbsp;weeks before and 6&amp;nbsp;months after surgery and included measures that describe the volume
 and pattern of ambulatory activity (number of steps per day, accumulation, diversity and variability of walking time), alongside
 standard measures for disease severity, freezing of gait, g...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5423718</comments>
            <pubDate>Tue, 15 Nov 2011 16:59:50 +0100</pubDate>
            <guid isPermaLink="false">5423718</guid>        </item>
        <item>
            <title>Personality traits in patients with Parkinson’s disease: assessment and clinical implications</title>
            <link>http://www.medworm.com/index.php?rid=5410445&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa61362w1421250p6%2F</link>
            <description>This study reviews empirical evidence on the association between personality traits and Parkinson’s disease (PD), with a twofold
 aim. First, to better identify non-motor symptoms, such as affective symptoms and personality changes, that could help to
 define the pre-motor phase of PD; second, to better understand the neurobiological bases of personality traits, a goal that
 is not fully accomplished by a purely anatomical approach. A literature review was performed on studies of personality traits
 in PD patients, in electronic databases ISI Web of Knowledge, Medline and PsychInfo, conducted in July 2011. We found evidence
 that the existence of a characteristic premorbid personality profile of PD patients is not actually sustained by robust empirical
 evidence, mainly due to the method...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410445</comments>
            <pubDate>Mon, 14 Nov 2011 16:58:53 +0100</pubDate>
            <guid isPermaLink="false">5410445</guid>        </item>
        <item>
            <title>Involvement of the capsular genu in reward-related feeding</title>
            <link>http://www.medworm.com/index.php?rid=5410446&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr544m23xtwk37548%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-011-6304-6Authors
		Keisuke Suzuki, Department of Neurology, Dokkyo Medical University, 880 Kitakobayashi, Mibu, Shimotsuga, Tochigi 321-0293, JapanTsubasa Sada, Department of Neurology, Dokkyo Medical University, 880 Kitakobayashi, Mibu, Shimotsuga, Tochigi 321-0293, JapanToshiki Nakamura, Department of Neurology, Rehabilitation Amakusa Hospital, Koshigaya, Saitama, JapanHidehiro Takekawa, Department of Neurology, Dokkyo Medical University, 880 Kitakobayashi, Mibu, Shimotsuga, Tochigi 321-0293, JapanKoichi Hirata, Department of Neurology, Dokkyo Medical University, 880 Kitakobayashi, Mibu, Shimotsuga, Tochigi 321-0293, Japan
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410446</comments>
            <pubDate>Mon, 14 Nov 2011 16:58:51 +0100</pubDate>
            <guid isPermaLink="false">5410446</guid>        </item>
        <item>
            <title>Functional neuroanatomy underlying the clinical subcategorization of minimally conscious state patients</title>
            <link>http://www.medworm.com/index.php?rid=5410447&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm0j3nkr660h36p5x%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Patients in a minimally conscious state (MCS) show restricted signs of awareness but are unable to communicate. We assessed
 cerebral glucose metabolism in MCS patients and tested the hypothesis that this entity can be subcategorized into MCS− (i.e.,
 patients only showing nonreflex behavior such as visual pursuit, localization of noxious stimulation and/or contingent behavior)
 and MCS+ (i.e., patients showing command following).
 
 
 Patterns of cerebral glucose metabolism were studied using [18F]-fluorodeoxyglucose-PET in 39 healthy volunteers (aged 46&amp;nbsp;±&amp;nbsp;18&amp;nbsp;years) and 27 MCS patients of whom 13 were MCS− (aged 49&amp;nbsp;±&amp;nbsp;19&amp;nbsp;years;
 4 traumatic; 21&amp;nbsp;±&amp;nbsp;23&amp;nbsp;months post injury) and 14 MCS+ (aged 43&amp;nbsp;±&amp;nbsp;19&amp;nbsp;years; 5...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410447</comments>
            <pubDate>Sat, 12 Nov 2011 06:47:58 +0100</pubDate>
            <guid isPermaLink="false">5410447</guid>        </item>
        <item>
            <title>Neurolathyrism: two Ethiopian case reports and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=5410449&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl426474186116611%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Neurolathyrism is a toxic myelopathy caused by ingestion of the Lathyrus sativus grasspea. An irreversible acute to subacute spastic paraparesis or quadriparesis ensues. Despite public education, new cases
 of this preventable disease still occur. Two Ethiopian cases of neurolathyrism are reported to illustrate the disease, followed
 by a literature review. Two teenage male farmers from the same village developed irreversible spastic myelopathy following
 L. sativus ingestion. There was no sensory, sphincter or bulbar dysfunction. Likely causative factors identified were increased consumption
 of L. sativus prior to and following disease onset, heavy physical exertion and male gender, similar to those reported in the literature.
 Neurolathyrism is an entirely preventabl...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410449</comments>
            <pubDate>Sat, 12 Nov 2011 06:47:56 +0100</pubDate>
            <guid isPermaLink="false">5410449</guid>        </item>
        <item>
            <title>Striatal hypermetabolism in limbic encephalitis</title>
            <link>http://www.medworm.com/index.php?rid=5410448&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F55202lp041130w05%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Striatal hypermetabolism on 18FDG-PET scan is a neuroradiological finding that has been described in association with autoimmune
 disorders such as Sydenham chorea, lupus or antiphospholipid syndrome. Here, we report three patients with non-paraneoplastic
 limbic encephalitis characterized by 18FDG-PET hypermetabolism of both striata, in contrast with diffuse hypometabolism in
 the rest of the brain. All patients developed subacute dementia, and antibodies to voltage-gated potassium channels were found
 in all cases. Brain metabolism and neurological status improved within a few months of immunosuppressive therapy. The finding
 of striatal hypermetabolism on 18FDG-PET images could thus be highly indicative of limbic encephalitis associated with anti-neuropil
 antibodies...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410448</comments>
            <pubDate>Sat, 12 Nov 2011 06:47:56 +0100</pubDate>
            <guid isPermaLink="false">5410448</guid>        </item>
        <item>
            <title>Focal pseudohypertrophy of the left hemi-tongue</title>
            <link>http://www.medworm.com/index.php?rid=5410450&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu2577x34415017h3%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-011-6310-8Authors
		Hiroshi Kataoka, Department of Neurology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara 634-8522, JapanSatoshi Ueno, Department of Neurology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara 634-8522, Japan
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410450</comments>
            <pubDate>Sat, 12 Nov 2011 06:47:55 +0100</pubDate>
            <guid isPermaLink="false">5410450</guid>        </item>
        <item>
            <title>Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years</title>
            <link>http://www.medworm.com/index.php?rid=5410451&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr37m605357x72236%2F</link>
            <description>This study represents the largest cohort of late-onset GSDII patients treated with
 ERT, and confirm a positive effect of treatment. These results, obtained in a large case series on therapy, indicate a favourable
 effect of ERT therapy, even in more advanced stage of the disease.
 
 
	Content Type Journal ArticleCategory Original CommunicationPages 1-7DOI 10.1007/s00415-011-6293-5Authors
		C. Angelini, Department of Neurosciences, University of Padova, Via Giustiniani 5, 35128 Padova, ItalyC. Semplicini, Department of Neurosciences, University of Padova, Via Giustiniani 5, 35128 Padova, ItalyS. Ravaglia, Department of Neurological Sciences, University of Pavia, Pavia, ItalyB. Bembi, Regional Coordination Centre for Rare Diseases, University Hospital S. Maria Della Misericordia, Udine, Ita...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410451</comments>
            <pubDate>Fri, 11 Nov 2011 16:44:37 +0100</pubDate>
            <guid isPermaLink="false">5410451</guid>        </item>
        <item>
            <title>Rapid improvement of tardive dyskinesia with tetrabenazine, clonazepam and clozapine combined: a naturalistic long-term follow-up study</title>
            <link>http://www.medworm.com/index.php?rid=5410452&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F56078381866mm70m%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Tardive dyskinesia (TD) is a complex involuntary movement disorder affecting about 23% of neuroleptic-treated patients. Our
 objective was to retrospectively analyze a combination of tetrabenazine (TBZ), clonazepam (CLONAZ) and clozapine (CLOZ) used
 simultaneously for TD in psychotic patients. Six patients with severe, unsuccessfully controlled TD were referred for treatment
 (mean age 51.5 years; three male; four schizophrenics; one bipolar disease; one borderline personality disorder). They were
 being treated with neuroleptics (classic, three; risperidone, two; olanzapine, one) and developed severe neck and buccolingual
 dyskinesias. At our clinic, all of them were treated simultaneously with TBZ (mean dose 141.6&amp;nbsp;mg); CLONAZ (mean dose 4.3&amp;nbsp;mg);
 and CLOZ (...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410452</comments>
            <pubDate>Wed, 09 Nov 2011 07:04:05 +0100</pubDate>
            <guid isPermaLink="false">5410452</guid>        </item>
        <item>
            <title>Concordance rates of Doppler ultrasound and CT angiography in the grading of carotid artery stenosis: a systematic literature review</title>
            <link>http://www.medworm.com/index.php?rid=5410453&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F177124p8874545w4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp; Physicians have been increasingly relying on noninvasive
 imaging methods to grade carotid stenosis. The accuracy of Doppler ultrasound (DUS)
 and CT angiography (CTA) versus intra-arterial angiography (IA) has been assessed in
 many studies and at least two meta-analyses. Here, we performed a systematic review
 of studies that compared DUS to CTA. In a PubMed review of the literature from 2000 to 2009, we found 12 studies that compared
 DUS and CTA-based grading of carotid stenosis. Only 4 of them
 included at least 20 patients and provided data to classify the diseased arteries into the
 following categories: mild, moderate or severe NASCET stenosis or occlusion. We extracted 431 arteries from 244 patients (range
 per study: 48–164). It was
 not possible to disting...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410453</comments>
            <pubDate>Tue, 08 Nov 2011 06:47:36 +0100</pubDate>
            <guid isPermaLink="false">5410453</guid>        </item>
        <item>
            <title>Investigation of autonomic function in idiopathic REM sleep behavior disorder</title>
            <link>http://www.medworm.com/index.php?rid=5410454&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg41583n57k2m9804%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Idiopathic REM sleep behavior disorder (iRBD) has been suggested as an early “pre-motor” stage of Parkinson’s disease (PD)
 in a significant proportion of cases. We investigated autonomic function in 15 consecutive iRBD patients and compared these
 findings to PD patients and healthy controls. All participants underwent cardiovascular autonomic function testing, and were
 rated on the COMPASS scale. Symptomatic orthostatic hypotension was present in two iRBD patients, two PD patients and none
 of the healthy controls. In the tilt table examination, blood pressure changes were similar between iRBD patients and healthy
 controls. In the PD group, blood pressure drops were more pronounced. In the orthostatic standing test, iRBD patients had
 higher blood pressure cha...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410454</comments>
            <pubDate>Tue, 08 Nov 2011 06:47:35 +0100</pubDate>
            <guid isPermaLink="false">5410454</guid>        </item>
        <item>
            <title>Vivid visual mental imagery in the absence of the primary visual cortex</title>
            <link>http://www.medworm.com/index.php?rid=5410455&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy25763387l14q53j%2F</link>
            <description>In this study, we show that in spite of his near-complete
 cortical blindness, SBR exhibits vivid visual mental imagery both behaviorally and when measured with functional magnetic
 resonance imaging. The pattern of cortical activation to visual mental imagery in SBR is indistinguishable from individual
 sighted subjects, in contrast to the visual perceptual responses, which are greatly attenuated.
 
 
	Content Type Journal ArticleCategory Original CommunicationPages 1-9DOI 10.1007/s00415-011-6299-zAuthors
		Holly Bridge, FMRIB Centre, John Radcliffe Hospital, University of Oxford, Oxford, OX3 9DU UKStephen Harrold, FMRIB Centre, John Radcliffe Hospital, University of Oxford, Oxford, OX3 9DU UKEmily A. Holmes, Department of Psychiatry, University of Oxford, Oxford, UKMark Stokes, Departmen...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410455</comments>
            <pubDate>Tue, 08 Nov 2011 06:47:34 +0100</pubDate>
            <guid isPermaLink="false">5410455</guid>        </item>
        <item>
            <title>Seroconversion of anti-aquaporin-4 antibody in NMO spectrum disorder: a case report</title>
            <link>http://www.medworm.com/index.php?rid=5410456&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F782q32631m258181%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-011-6288-2Authors
		Masahiro Mori, Department of Neurology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670 JapanNaoki Kawaguchi, Department of Neurology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670 JapanAkiyuki Uzawa, Department of Neurology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670 JapanYuhko Nemoto, Department of Neurology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670 JapanSaeko Masuda, Department of Neurology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670 JapanSatoshi Kuwabara, Department of ...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410456</comments>
            <pubDate>Tue, 08 Nov 2011 06:47:33 +0100</pubDate>
            <guid isPermaLink="false">5410456</guid>        </item>
        <item>
            <title>Sporadic juvenile amyotrophic lateral sclerosis caused by mutant FUS/TLS: possible association of mental retardation with this mutation</title>
            <link>http://www.medworm.com/index.php?rid=5389907&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe65q270118104125%2F</link>
            <description>We present two cases of patients with juvenile amyotrophic lateral sclerosis (ALS), who had no history of familial ALS. The
 symptoms of both patients started as weakness of the unilateral upper limb and neck, and extended to bulbar and respiratory
 weakness in a relatively short period. Of note, the first patient was mentally retarded before the onset of weakness. Fused in sarcoma/translocated in liposarcoma (FUS/TLS) gene analyses revealed mutations of p. G492EfsX527 (c. 1475delG), which is a novel deletion/frameshift mutation, in the
 first patient and p. R514S mutation (c. 1542G&amp;nbsp;&amp;gt;&amp;nbsp;T) in the second patient. Molecular analysis revealed that the mutant FUS/TLS,
 especially the deletion/frameshift mutation, showed significant cytoplasmic localization in transfected motor neuro...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5389907</comments>
            <pubDate>Sat, 05 Nov 2011 15:43:16 +0100</pubDate>
            <guid isPermaLink="false">5389907</guid>        </item>
        <item>
            <title>Zoophilia and impulse control disorder in a patient with Parkinson disease</title>
            <link>http://www.medworm.com/index.php?rid=5389910&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5627071613622092%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-2DOI 10.1007/s00415-011-6270-zAuthors
		Gabriela Raina, Parkinson’s Disease and Movement Disorders Program, Hospital de Clínicas “José de San Martín”, University of Buenos Aires, Buenos Aires, ArgentinaMaria Graciela Cersosimo, Parkinson’s Disease and Movement Disorders Program, Hospital de Clínicas “José de San Martín”, University of Buenos Aires, Buenos Aires, ArgentinaFederico Micheli, Parkinson’s Disease and Movement Disorders Program, Hospital de Clínicas “José de San Martín”, University of Buenos Aires, Buenos Aires, Argentina
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5389910</comments>
            <pubDate>Sat, 05 Nov 2011 15:43:15 +0100</pubDate>
            <guid isPermaLink="false">5389910</guid>        </item>
        <item>
            <title>Use of intrathecal clonidine in patients with multiple sclerosis or spastic paraparesis</title>
            <link>http://www.medworm.com/index.php?rid=5389909&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd7v3905tp7p62137%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-3DOI 10.1007/s00415-011-6290-8Authors
		Joseph K. Ho, Multiple Sclerosis Research Center of New York, 521 West 57th Street, 4th Floor, New York, NY 10019, USASaud A. Sadiq, Multiple Sclerosis Research Center of New York, 521 West 57th Street, 4th Floor, New York, NY 10019, USA
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5389909</comments>
            <pubDate>Sat, 05 Nov 2011 15:43:15 +0100</pubDate>
            <guid isPermaLink="false">5389909</guid>        </item>
        <item>
            <title>Transcranial sonography in pantothenate kinase-associated neurodegeneration</title>
            <link>http://www.medworm.com/index.php?rid=5389908&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fwt440727138n8542%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;After it was reported that increased tissue iron concentrations were associated with increased echogenicity of the substantia
 nigra (SN) obtained with transcranial sonography (TCS) in animal and postmortem studies, our goal was to use this method in
 a disorder characterized with iron accumulation in human brain tissue. Therefore, magnetic resonance imaging (MRI) and TCS
 were conducted in 5&amp;nbsp;unrelated patients with pantothenate kinase-associated neurodegeneration (PKAN), caused by PANK2 mutations. All patients had an eye of the tiger sign. Hypointense lesions on the T2-weighted MRI images were restricted to
 the globus pallidus (GP) and SN. TCS also revealed bilateral hyperechogenicity restricted to the LN and SN, with normal DTV
 values. Both TCS and MRI studies ...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5389908</comments>
            <pubDate>Sat, 05 Nov 2011 15:43:15 +0100</pubDate>
            <guid isPermaLink="false">5389908</guid>        </item>
        <item>
            <title>Detection of anti-glutamate receptor ε2 and anti-N-methyl-d-aspartate receptor antibodies in a patient with sporadic Creutzfeldt–Jakob disease</title>
            <link>http://www.medworm.com/index.php?rid=5389914&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F086x50281q273353%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-4DOI 10.1007/s00415-011-6291-7Authors
		Koji Fujita, Department of Clinical Neuroscience, The University of Tokushima Graduate School, 3-18-15 Kuramoto-cho, Tokushima, 770-8503 JapanTatsuhiko Yuasa, Department of Neurology, Kamagaya-Chiba Medical Center for Intractable Neurological Disease, Kamagaya General Hospital, Kamagaya, 273-0121 JapanYukitoshi Takahashi, National Epilepsy Center, Shizuoka Institute of Epilepsy and Neurological Disorders, Shizuoka, 420-8688 JapanKeiko Tanaka, Department of Neurology, Kanazawa Medical University, Kahokugun, 920-0293 JapanShuji Hashiguchi, Department of Neurology, Tokushima National Hospital, National Hospital Organization, Yoshinogawa, 776-8585 JapanKatsuhito Adachi, Department of Neu...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5389914</comments>
            <pubDate>Fri, 04 Nov 2011 16:51:06 +0100</pubDate>
            <guid isPermaLink="false">5389914</guid>        </item>
        <item>
            <title>Clinical and MRI patterns of pericallosal artery infarctions: the significance of supplementary motor area lesions</title>
            <link>http://www.medworm.com/index.php?rid=5389913&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F86l3k638584p6386%2F</link>
            <description>We report a case series of patients with isolated infarctions
 of the pericallosal (PC) artery territory. We analyzed 36 consecutive patients presenting over a 10-year period with isolated
 PC artery territory infarctions (15 left-sided, 19 right-sided, 2 bilateral) regarding clinical symptoms as well as MRI findings.
 Analysis of DWI lesion pattern showed complete PC artery infarctions in three patients. The majority of patients had partial
 infarctions predominantly involving either the superior frontal gyrus (n&amp;nbsp;=&amp;nbsp;12), the corpus callosum (n&amp;nbsp;=&amp;nbsp;1) or both (n&amp;nbsp;=&amp;nbsp;20). Hemodynamic lesion patterns were found in 13 patients, while multiple cortical emboli occurred in six. Distal pathology
 of the ACA (n&amp;nbsp;=&amp;nbsp;13) was the most frequent MRA finding. Core sympto...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5389913</comments>
            <pubDate>Fri, 04 Nov 2011 16:51:06 +0100</pubDate>
            <guid isPermaLink="false">5389913</guid>        </item>
        <item>
            <title>The hemodynamic status within 24 h after intravenous thrombolysis predicts infarct growth in acute ischemic stroke</title>
            <link>http://www.medworm.com/index.php?rid=5389912&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F12l11566708h8w2p%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A rapid and complete recanalization of the occluded artery is the ideal goal when intravenous (IV) recombinant tissue plasminogen
 activator (rt-PA) is administrated to patients with acute ischemic stroke, i.e., limiting the ongoing ischemia to achieve
 a better outcome. We explored the effect of complete versus partial recanalization of the occluded intracranial artery after
 IV thrombolysis on the infarct growth and evaluated the functional impact. Using diffusion-weighted (DWI) volumetric measurements
 before rt-PA administration (DWI1) and 24&amp;nbsp;h later (DWI2), we calculated the infarct growth in 36 consecutive patients with ischemic stroke treated with IV rt-PA, with the formula
 DWI2/DWI1. Recanalization of the affected artery was assessed by transcranial Dopple...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5389912</comments>
            <pubDate>Fri, 04 Nov 2011 16:51:06 +0100</pubDate>
            <guid isPermaLink="false">5389912</guid>        </item>
        <item>
            <title>Factors related to recurrence of paradoxical cerebral embolism due to patent foramen ovale</title>
            <link>http://www.medworm.com/index.php?rid=5389911&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F91317301w9kr0874%2F</link>
            <description>In conclusion, size of the PFO and presence of a massive bubble
 were considered to be factors associated with recurrence of ischemic stroke due to PFO.
 
 
	Content Type Journal ArticleCategory Original CommunicationPages 1-5DOI 10.1007/s00415-011-6297-1Authors
		Takuya Fukuoka, Department of Neurology and Cerebrovascular Medicine, Saitama International Medical Center, Saitama Medical University, 1397-1 Yamane, Hidaka, Saitama 350-1298, JapanTomohisa Dembo, Department of Neurology and Cerebrovascular Medicine, Saitama International Medical Center, Saitama Medical University, 1397-1 Yamane, Hidaka, Saitama 350-1298, JapanHarumitu Nagoya, Department of Neurology and Cerebrovascular Medicine, Saitama International Medical Center, Saitama Medical University, 1397-1 Yamane, Hidaka, Saitama 350...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5389911</comments>
            <pubDate>Fri, 04 Nov 2011 16:51:06 +0100</pubDate>
            <guid isPermaLink="false">5389911</guid>        </item>
        <item>
            <title>Hereditary neuropathy with liability to pressure palsy combined with suspected schwannomas of the peroneal and radial nerves</title>
            <link>http://www.medworm.com/index.php?rid=5365412&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp4l8176808113182%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-3DOI 10.1007/s00415-011-6287-3Authors
		Masaki Ohyagi, Department of Neurology and Neurological Science, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8519 JapanNobuo Sanjo, Department of Neurology and Neurological Science, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8519 JapanTakanori Yokota, Department of Neurology and Neurological Science, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8519 JapanHidehiro Mizusawa, Department of Neurology and Neurological Science, Graduate School of Medical an...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5365412</comments>
            <pubDate>Fri, 28 Oct 2011 16:59:38 +0100</pubDate>
            <guid isPermaLink="false">5365412</guid>        </item>
        <item>
            <title>Recent advances in the diagnosis and treatment of balance disorders</title>
            <link>http://www.medworm.com/index.php?rid=5365414&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn406128435w54741%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Here we summarize the recent progress made in the diagnosis and treatment of balance and gait disorders. Focusing on work
 published in the Journal of Neurology in 2010 and 2011, we have found evidence for the following clinically relevant statements: (1) the exclusion of stroke in
 acute vestibular syndromes is based on the bedside clinical findings; (2) the risk of developing secondary somatoform vertigo
 is predictable; it is especially high in patients with vestibular migraine; (3) postural imbalance and falls in Parkinson
 syndromes are related to dysfunction of the cholinergic midbrain thalamic axis; (4) aminopyridines improve a variety of cerebellar
 parameters including central nystagmus and gait variability.
 
 
	Content Type Journal ArticleCategory Medical Pro...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5365414</comments>
            <pubDate>Fri, 28 Oct 2011 16:59:36 +0100</pubDate>
            <guid isPermaLink="false">5365414</guid>        </item>
        <item>
            <title>Perrault syndrome: further evidence for genetic heterogeneity</title>
            <link>http://www.medworm.com/index.php?rid=5365413&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx24q564214462636%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-3DOI 10.1007/s00415-011-6285-5Authors
		Emma M. Jenkinson, Genetic Medicine, Manchester Academic Health Services Centre (MAHSC), St. Mary’s Hospital, University of Manchester, Manchester, M13 9WL UKJill Clayton-Smith, Genetic Medicine, Manchester Academic Health Services Centre (MAHSC), St. Mary’s Hospital, University of Manchester, Manchester, M13 9WL UKSarju Mehta, East Anglian Medical Genetics Service, Addenbrookes Hospital, Cambridge, CB2 0QQ UKChristopher Bennett, Yorkshire Regional Genetics Service, Ashley Wing, St James’s University Hospital, Leeds, LS9 7TF UKWillie Reardon, National Centre for Medical Genetics, Our Lady’s Hospital for Sick Children, Crumlin, Dublin 12, IrelandAndrew Green, National Centre f...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5365413</comments>
            <pubDate>Fri, 28 Oct 2011 16:59:36 +0100</pubDate>
            <guid isPermaLink="false">5365413</guid>        </item>
        <item>
            <title>ENS Communications</title>
            <link>http://www.medworm.com/index.php?rid=5365416&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F511858nq673285nt%2F</link>
            <description>Content Type Journal ArticleCategory ENS CommunicationsPages 1-3DOI 10.1007/s00415-011-6283-7

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5365416</comments>
            <pubDate>Fri, 28 Oct 2011 16:59:35 +0100</pubDate>
            <guid isPermaLink="false">5365416</guid>        </item>
        <item>
            <title>Judgment of FLAIR signal change in DWI–FLAIR mismatch determination is a challenge to clinicians</title>
            <link>http://www.medworm.com/index.php?rid=5365415&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F623w4k071r6681g2%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-3DOI 10.1007/s00415-011-6284-6Authors
		Annerose Ziegler, Department of Neurology, Charite, Universitätsmedizin Berlin, Campus Benjamin Franklin, Hindenburgdamm 30, 12203 Berlin, GermanyMartin Ebinger, Department of Neurology, Charite, Universitätsmedizin Berlin, Campus Benjamin Franklin, Hindenburgdamm 30, 12203 Berlin, GermanyJochen B. Fiebach, Department of Neurology, Charite, Universitätsmedizin Berlin, Campus Benjamin Franklin, Hindenburgdamm 30, 12203 Berlin, GermanyHeinrich J. Audebert, Department of Neurology, Charite, Universitätsmedizin Berlin, Campus Benjamin Franklin, Hindenburgdamm 30, 12203 Berlin, GermanyStefanie Leistner, Department of Neurology, Charite, Universitätsmedizin Berlin, Campus Benjamin Fra...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5365415</comments>
            <pubDate>Fri, 28 Oct 2011 16:59:35 +0100</pubDate>
            <guid isPermaLink="false">5365415</guid>        </item>
        <item>
            <title>Executive dysfunction in frontotemporal dementia is related to abnormalities in frontal white matter tracts</title>
            <link>http://www.medworm.com/index.php?rid=5365418&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fln74617310j260x5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cognitive deficits in behavioral-variant frontotemporal dementia (bvFTD) and AD are linked to frontal and temporal lobe gray
 matter (GM) pathology. The aim of this study was to assess the relative contribution of white (WM) and GM abnormalities to
 cognitive dysfunction in bvFTD and AD. Fractional anisotropy (FA) for the corpus callosum, cingulum (Cg), and uncinate fasciculus
 (Unc) was determined in 17 bvFTD and 10 AD patients who underwent neuropsychological testing. Regressions were performed to
 assess the relative contribution of WM and GM abnormalities to cognitive deficits. Multiple regression analysis revealed that
 in bvFTD, the left anterior Cg FA was related to executive function, the right anterior Cg FA to visual-spatial attention
 and working memory, the ...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5365418</comments>
            <pubDate>Fri, 28 Oct 2011 16:59:34 +0100</pubDate>
            <guid isPermaLink="false">5365418</guid>        </item>
        <item>
            <title>Stroke: new TIA definition, new anticoagulation, no stenting</title>
            <link>http://www.medworm.com/index.php?rid=5365417&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv877522488548887%2F</link>
            <description>Content Type Journal ArticleCategory Journal ClubPages 1-3DOI 10.1007/s00415-011-6282-8Authors
		M. Strupp, Department of Neurology and IFBLMU, Campus Grosshadern, University Hospital Munich, Marchioninistr. 15, 81377 Munich, Germany
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5365417</comments>
            <pubDate>Fri, 28 Oct 2011 16:59:34 +0100</pubDate>
            <guid isPermaLink="false">5365417</guid>        </item>
        <item>
            <title>Pure left hippocampal stroke: a transient global amnesia-plus syndrome</title>
            <link>http://www.medworm.com/index.php?rid=5365419&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4n3h817lh8p06428%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorsPages 1-4DOI 10.1007/s00415-011-6296-2Authors
		Antonio Carota, Hildebrand Clinic, Rehabilitation Center, 6614 Brissago, SwitzerlandAndreas P. Lysandropoulos, Neurology Service, CHUV, Lausanne, SwitzerlandPasquale Calabrese, Department of Psychology, University of Basel, Basel, Switzerland
	

	
		Journal Journal of NeurologyOnline ISSN 1432-1459Print ISSN 0340-5354 (Source: Journal of Neurology)</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5365419</comments>
            <pubDate>Fri, 28 Oct 2011 16:59:33 +0100</pubDate>
            <guid isPermaLink="false">5365419</guid>        </item>
        <item>
            <title>Stroke and Fabry disease</title>
            <link>http://www.medworm.com/index.php?rid=5365420&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb0645565qn20283v%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Fabry disease (FD) is a rare inherited disorder of the metabolism, associated with renal, cardiac, and cerebrovascular complications.
 Ischemic and hemorrhagic stroke in FD present with a similar proportion to that observed in the general population, but usually
 at an early age. Ischemic stroke may result from cardiac embolism, large and small vessel disease, while hemorrhagic stroke
 is usually attributed to hypertension. Deposition of glycosphingolipids in endothelial cells results in a specific FD vasculopathy
 that contributes to the different vascular phenotypes. Neuroimaging features of cerebrovascular involvement in FD include
 white matter lesions, dolichoectasia, and the “pulvinar sign”, a T1 MRI hyperintensity of the posterior thalamus. The role
 of enzym...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5365420</comments>
            <pubDate>Fri, 28 Oct 2011 16:59:31 +0100</pubDate>
            <guid isPermaLink="false">5365420</guid>        </item>
        <item>
            <title>Hyperdensity on non-contrast CT immediately after intra-arterial revascularization</title>
            <link>http://www.medworm.com/index.php?rid=5349696&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr48x312728523n19%2F</link>
            <description>In conclusion,
 our results showed that although hyperdensity on NCCT images obtained immediately after IAR had a moderate predictive value
 for HT, there were limitations to the prediction of subsequent parenchymal hematoma and symptomatic intracranial hemorrhage,
 with a low specificity and a low positive predictive value.
 
 
	Content Type Journal ArticleCategory Original CommunicationPages 1-8DOI 10.1007/s00415-011-6281-9Authors
		Joon-Tae Kim, Department of Neurology, Cerebrovascular Center, Chonnam National University Hospital, Gwangju, KoreaSuk-Hee Heo, Department of Radiology, Chonnam National University Hwasun Hospital, Hwasun, KoreaBang-Hoon Cho, Department of Neurology, Cerebrovascular Center, Chonnam National University Hospital, Gwangju, KoreaSeong-Min Choi, Department of Neur...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5349696</comments>
            <pubDate>Fri, 21 Oct 2011 06:10:02 +0100</pubDate>
            <guid isPermaLink="false">5349696</guid>        </item>
        <item>
            <title>Parkinsonism following bilateral hypoxic-ischemic lesions of the striatum</title>
            <link>http://www.medworm.com/index.php?rid=5349697&amp;cid=s_33364_25_f&amp;fid=33364&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9717826473m0u13w%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 40-year-old white male received cardio-pulmonary resuscitation after cardiac arrest due to an epileptic status. Four&amp;nbsp;months
 after the incident he developed an akinetic-rigid syndrome and a postural tremor more pronounced on the right side of the
 body. Brain imaging revealed bilateral lesions of the putamen and caudate nucleus. Levodopa improved bradykinesia and muscular
 rigidity, but not the postural tremor.
 
 
	Content Type Journal ArticleCategory Original CommunicationPages 1-3DOI 10.1007/s00415-011-6274-8Authors
		Dennis A. Nowak, Neurologische Fachklinik Kipfenberg, Kindingerstrasse 13, 85110 Kipfenberg, GermanyAndreas Bock, Neurologische Fachklinik Kipfenberg, Kindingerstrasse 13, 85110 Kipfenberg, GermanyMatthias Ponfick, Neurologische Fachklinik Kipfen...</description>
            <author>Journal of Neurology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5349697</comments>
            <pubDate>Fri, 21 Oct 2011 06:10:00 +0100</pubDate>
            <guid isPermaLink="false">5349697</guid>        </item>
    </channel>
</rss>

