<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0">
    <channel>
        <title>Movement Disorders 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 'Movement Disorders' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Movement+Disorders&t=Movement+Disorders&s=Search&f=source]]></link>
        <lastBuildDate>Wed, 08 Feb 2012 20:43:24 +0100</lastBuildDate>
        <item>
            <title>Comparison of enrollees and decliners of Parkinson disease sham surgery trials</title>
            <link>http://www.medworm.com/index.php?rid=5668710&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24940</link>
            <description>AbstractConcerns have been raised that persons with serious illnesses participating in high‐risk research, such as PD patients in sham surgery trials, have unrealistic expectations and are vulnerable to exploitation. A comparison of enrollees and decliners of such research may provide insights about the adequacy of decision making by potential subjects. We compared 61 enrollees and 10 decliners of two phase II neurosurgical intervention (i.e., cellular and gene transfer) trials for PD regarding their demographic and clinical status, perceptions and attitudes regarding research risks, potential direct benefit, and societal benefit, and perspectives on the various potential reasons for and against participation. In addition to bivariate analyses, a logistic regression model examined variab...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5668710</comments>
            <pubDate>Tue, 07 Feb 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5668710</guid>        </item>
        <item>
            <title>Postmortem observation of collagenous lead tip region fibrosis as a rare complication of DBS</title>
            <link>http://www.medworm.com/index.php?rid=5668709&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24916</link>
            <description>Conclusions:We are not aware of any prior reports of such a dramatic reaction to DBS placement to date. © 2012 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5668709</comments>
            <pubDate>Tue, 07 Feb 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5668709</guid>        </item>
        <item>
            <title>Abnormal DAT SCAN in a patient with parkinsonism after a midbrain ischemic lesion</title>
            <link>http://www.medworm.com/index.php?rid=5668712&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24890</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5668712</comments>
            <pubDate>Mon, 06 Feb 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5668712</guid>        </item>
        <item>
            <title>T1‐Weighted MRI shows stage‐dependent substantia nigra signal loss in Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5668711&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24067</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5668711</comments>
            <pubDate>Mon, 06 Feb 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5668711</guid>        </item>
        <item>
            <title>Increased medial orbitofrontal [18F]fluorodopa uptake in Parkinsonian impulse control disorders</title>
            <link>http://www.medworm.com/index.php?rid=5660905&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24941</link>
            <description>Conclusions:Increased monoaminergic activity in the medial orbitofrontal cortex might be associated with increased sensitivity for ICDs under dopamine‐replacement therapy in PD. © 2012 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660905</comments>
            <pubDate>Sun, 05 Feb 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5660905</guid>        </item>
        <item>
            <title>Role of the external oblique muscle in upper camptocormia for patients with Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5650103&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24930</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650103</comments>
            <pubDate>Mon, 30 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650103</guid>        </item>
        <item>
            <title>Lacosamide in paroxysmal kinesigenic dyskinesia</title>
            <link>http://www.medworm.com/index.php?rid=5650102&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24928</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650102</comments>
            <pubDate>Mon, 30 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650102</guid>        </item>
        <item>
            <title>Brain iron deposition fingerprints in Parkinson's disease and progressive supranuclear palsy</title>
            <link>http://www.medworm.com/index.php?rid=5650101&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24926</link>
            <description>We report that an abnormal brain iron accumulation is a marker for ongoing neurodegeneration in both conditions, but the conditions differ with respect to the anatomical distribution of these accumulations. We analyzed quantitative T2′ maps as markers of regional brain iron content from PD and progressive supranuclear palsy patients and compared them to age‐matched control subjects. T2‐weighted and T2*‐weighted images were acquired in 30 PD patients, 12 progressive supranuclear palsy patients, and 24 control subjects at 1.5 Tesla. Mean T2′ values were determined in regions‐of‐interest in the basal ganglia, thalamus, and white matter within each hemisphere. The main findings were shortened T2′ values in the caudate nucleus, globus pallidus, and putamen in progressive supranu...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650101</comments>
            <pubDate>Mon, 30 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650101</guid>        </item>
        <item>
            <title>Association of BDNF Met66Met polymorphism with arm tremor in cervical dystonia</title>
            <link>http://www.medworm.com/index.php?rid=5650100&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24922</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650100</comments>
            <pubDate>Mon, 30 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650100</guid>        </item>
        <item>
            <title>A new hyperekplexia family with a recessive frameshift mutation in the GLRA1 gene</title>
            <link>http://www.medworm.com/index.php?rid=5650099&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24917</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650099</comments>
            <pubDate>Mon, 30 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650099</guid>        </item>
        <item>
            <title>Toward an animal model of restless legs syndrome?</title>
            <link>http://www.medworm.com/index.php?rid=5650098&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24905</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650098</comments>
            <pubDate>Mon, 30 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650098</guid>        </item>
        <item>
            <title>Rivastigmine as alternative treatment for refractory REM behavior disorder in Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5650097&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24909</link>
            <description>Conclusions:The results of this pilot trial need to be confirmed by further studies on a larger number of patients. © 2012 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650097</comments>
            <pubDate>Mon, 30 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650097</guid>        </item>
        <item>
            <title>Unilateral thalamic stimulation safely improved fragile X–associated tremor ataxia: A case report</title>
            <link>http://www.medworm.com/index.php?rid=5639523&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24923</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639523</comments>
            <pubDate>Fri, 27 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5639523</guid>        </item>
        <item>
            <title>The complex movement disorder of Kasabach–Merritt syndrome associated with a basal ganglia lesion</title>
            <link>http://www.medworm.com/index.php?rid=5639522&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24911</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639522</comments>
            <pubDate>Fri, 27 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5639522</guid>        </item>
        <item>
            <title>Autonomic dysfunction in PD during sleep</title>
            <link>http://www.medworm.com/index.php?rid=5639521&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24897</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639521</comments>
            <pubDate>Fri, 27 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5639521</guid>        </item>
        <item>
            <title>“Dancing feet dyskinesias”: A clue to parkin gene mutations</title>
            <link>http://www.medworm.com/index.php?rid=5639520&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24894</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639520</comments>
            <pubDate>Fri, 27 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5639520</guid>        </item>
        <item>
            <title>Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia</title>
            <link>http://www.medworm.com/index.php?rid=5639519&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24064</link>
            <description>Conclusions:The rare genetic ataxias examined here do not significantly contribute to sporadic cerebellar ataxia in our tertiary care population. © 2012 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639519</comments>
            <pubDate>Fri, 27 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5639519</guid>        </item>
        <item>
            <title>Echoes from childhood—imitation in Gilles de la Tourette Syndrome</title>
            <link>http://www.medworm.com/index.php?rid=5630532&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24913</link>
            <description>Conclusions:Echopraxia is a hallmark of Tourette syndrome. © 2012 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5630532</comments>
            <pubDate>Wed, 25 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5630532</guid>        </item>
        <item>
            <title>Diagnostic criteria for mild cognitive impairment in Parkinson's disease: Movement Disorder Society Task Force guidelines</title>
            <link>http://www.medworm.com/index.php?rid=5630533&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24893</link>
            <description>This article provides guidelines to characterize the clinical syndrome and methods for its diagnosis. The criteria will require validation, and possibly refinement, as additional research improves our understanding of the epidemiology, presentation, neurobiology, assessment, and long‐term course of this clinical syndrome. These diagnostic criteria will support future research efforts to identify at the earliest stage those PD patients at increased risk of progressive cognitive decline and dementia who may benefit from clinical interventions at a predementia stage. © 2012 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5630533</comments>
            <pubDate>Tue, 24 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5630533</guid>        </item>
        <item>
            <title>Changes in neuronal firing rate in the subthalamic nucleus with Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5611152&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24899</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611152</comments>
            <pubDate>Thu, 19 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611152</guid>        </item>
        <item>
            <title>No evidence for differential methylation of α‐synuclein in leukocyte DNA of Parkinson's Disease patients</title>
            <link>http://www.medworm.com/index.php?rid=5611151&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24907</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611151</comments>
            <pubDate>Thu, 19 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611151</guid>        </item>
        <item>
            <title>Apathy in parkinson's disease: Diagnostic and etiological dilemmas</title>
            <link>http://www.medworm.com/index.php?rid=5599397&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24061</link>
            <description>AbstractAbout one‐third of patients with Parkinson's disease (PD) are diagnosed with apathy in cross‐sectional studies. However, once patients with concomitant depression and dementia are excluded, the frequency of apathy drops to 5% to 10%. Several scales have been recommended to rate apathy in PD, but specific psychiatric interviews have not been developed, and recently proposed standardized diagnostic criteria are still in the validation process. Most studies assessing the association between subthalamic deep brain stimulation (STN‐DBS) and apathy have reported a relative increase in the frequency and severity of apathy, although discrepant findings have also been reported. Several mechanisms to explain apathy in PD have been proposed, from dopaminergic imbalances in frontal‐bas...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5599397</comments>
            <pubDate>Wed, 11 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5599397</guid>        </item>
        <item>
            <title>Impaired olfaction and other prodromal features in the Parkinson At‐Risk Syndrome study</title>
            <link>http://www.medworm.com/index.php?rid=5599396&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24892</link>
            <description>AbstractTo test the association between impaired olfaction and other prodromal features of PD in the Parkinson At‐Risk Syndrome Study. The onset of olfactory dysfunction in PD typically precedes motor features, suggesting that olfactory testing could be used as a screening test. A combined strategy that uses other prodromal nonmotor features, along with olfactory testing, may be more efficient than hyposmia alone for detecting the risk of PD. Individuals with no neurological diagnosis completed a mail survey, including the 40‐item University of Pennsylvania Smell Identification Test, and questions on prodromal features of PD. The frequency of reported nonmotor features was compared across individuals with and without hyposmia. A total of 4,999 subjects completed and returned the survey...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5599396</comments>
            <pubDate>Wed, 11 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5599396</guid>        </item>
        <item>
            <title>No correlation of substantia nigra echogenicity and nigrostriatal degradation in Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5599395&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24070</link>
            <description>Conclusions:Substantia nigra hyperechogenicity does not reflect the degree of the nigrostriatal degeneration or the clinical state of the disease progression. © 2012 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5599395</comments>
            <pubDate>Wed, 11 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5599395</guid>        </item>
        <item>
            <title>Painless legs and moving toes from parasagittal meningioma</title>
            <link>http://www.medworm.com/index.php?rid=5599394&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24887</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5599394</comments>
            <pubDate>Wed, 11 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5599394</guid>        </item>
        <item>
            <title>Prevalence of pain in Parkinson's disease: A systematic review using the modified QUADAS tool</title>
            <link>http://www.medworm.com/index.php?rid=5599398&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24054</link>
            <description>AbstractPain has been studied more intensely as a symptom of Parkinson's disease (PD) in recent years. However, studies on the characteristics and prevalence of pain in PD have yielded conflicting results, prompting us to do a systematic review of the literature. A systematic review of the literature was conducted, using different databases. The last inclusion date was March 15, 2011. The modified Quality Assessment of Diagnostic Accuracy Studies (QUADAS) tool was used, which is especially designed for judging prevalence studies on their methodological quality. Only articles that met the predefined criteria were used in this review. We found 18 articles, of which only 8 met the methodological criteria. Prevalence frequency ranges from 40% to 85% with a mean of 67.6%. Pain is most frequentl...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5599398</comments>
            <pubDate>Mon, 09 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5599398</guid>        </item>
        <item>
            <title>Evidence of an association between the scavenger receptor class B member 2 gene and Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5562001&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24886</link>
            <description>AbstractLysosomal protein 2 (LIMP2), the product of the scavenger receptor class B member 2 (SCARB2) gene, is a ubiquitously expressed transmembrane protein that is the mannose‐6‐phosphate–independent receptor for glucocerebrosidase (β‐GCase); a deficiency in this protein causes Gaucher disease. Several studies have shown a link between mutations in the β‐GCase gene and diseases characterized clinically by Parkinsonism and by the presence of Lewy body–related pathology. We hypothesized that genetic variants in the SCARB2 gene could be risk factors for Parkinson's disease (PD). A candidate‐gene study of 347 Greek patients with sporadic PD and 329 healthy controls was conducted to investigate the association between 5 polymorphisms in the SCARB2 gene (rs6824953, rs6825004, rs...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5562001</comments>
            <pubDate>Thu, 05 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5562001</guid>        </item>
        <item>
            <title>Taking sides: Is handedness involved in motor asymmetry of Parkinson's disease?</title>
            <link>http://www.medworm.com/index.php?rid=5562000&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24048</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5562000</comments>
            <pubDate>Thu, 05 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5562000</guid>        </item>
        <item>
            <title>Re‐emergent tremor in a dystonic SWEDD case</title>
            <link>http://www.medworm.com/index.php?rid=5561999&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24040</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5561999</comments>
            <pubDate>Thu, 05 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5561999</guid>        </item>
        <item>
            <title>Basic parameters of articulatory movements and acoustics in individuals with Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5562008&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24888</link>
            <description>AbstractIt has long been recognized that lesions of the basal ganglia frequently result in dysarthria, in part because many individuals with Parkinson's disease (PD) have impaired speech. Earlier studies of speech production in PD using perceptual, acoustic, and/or kinematic analyses have yielded mixed findings about the characteristics of articulatory movements underlying hypokinetic dysarthria associated with PD: in some cases reporting reduced articulatory output, and in other instances revealing orofacial movement parameters within the normal range. The central aim of this experiment was to address these inconsistencies by providing an integrative description of basic kinematic and acoustic parameters of speech production in individuals with PD. Recordings of lip and jaw movements and ...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5562008</comments>
            <pubDate>Wed, 04 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5562008</guid>        </item>
        <item>
            <title>The atypical subthalamic nucleus—an anatomical variant relevant for stereotactic targeting</title>
            <link>http://www.medworm.com/index.php?rid=5562007&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24902</link>
            <description>Conclusion:An atypical position of the STN does not need to complicate DBS surgery, if detected by a combination of MRI‐based targeting and electrophysiological guidance. © 2012 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5562007</comments>
            <pubDate>Wed, 04 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5562007</guid>        </item>
        <item>
            <title>Diagnostic agreement in patients with psychogenic movement disorders</title>
            <link>http://www.medworm.com/index.php?rid=5562006&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24903</link>
            <description>Conclusions:Diagnosis according to clinical available criteria for PMD yields poor diagnostic agreement. © 2012 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5562006</comments>
            <pubDate>Wed, 04 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5562006</guid>        </item>
        <item>
            <title>Deep brain stimulation of the subthalamic nucleus improves sense of well‐being in parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5562005&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24035</link>
            <description>AbstractDeep brain stimulation of the subthalamic nucleus is an effective treatment for the motor symptoms of Parkinson's disease. Although a range of psychiatric and behavioral problems have been documented following deep brain stimulation, the short‐term effects of subthalamic nucleus stimulation on patients' mood have only been investigated in a few studies. Our aim was to compare self‐reported mood in Parkinson's patients with deep brain stimulation of the subthalamic nucleus ON versus OFF. Twenty‐three Parkinson's patients with bilateral deep brain stimulation of the subthalamic nucleus and 11 unoperated Parkinson's patients completed a mood visual analogue scale twice. Operated patients were tested with deep brain stimulation of the subthalamic nucleus both ON and OFF. All were...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5562005</comments>
            <pubDate>Wed, 04 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5562005</guid>        </item>
        <item>
            <title>Erythropoietin in friedreich ataxia: No effect on frataxin in a randomized controlled trial</title>
            <link>http://www.medworm.com/index.php?rid=5562004&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24066</link>
            <description>AbstractBackground:Friedreich ataxia is a rare disease caused by GAA‐trinucleotide‐repeat expansions in the frataxin gene, leading to marked reduction of qualitatively normal frataxin protein. Recently, human recombinant erythropoietin was reported to increase frataxin levels in patients with Friedreich ataxia.Methods:We performed a 6‐month, randomized placebo‐controlled, double‐blind, dose‐response pilot trial to assess the safety and efficacy of erythropoietin in increasing frataxin levels. Sixteen adult patient with Friedreich ataxia were randomly assigned to erythropoietin (n = 11) or matching placebo (n = 5). All patients continued Idebenone treatment (5 mg/kg/day). Treatment consisted of a 6‐month scaling‐up phase, in which erythropoietin was administered intravenousl...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5562004</comments>
            <pubDate>Wed, 04 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5562004</guid>        </item>
        <item>
            <title>Systematic evaluation of augmentation during treatment with ropinirole in restless legs syndrome (Willis‐Ekbom Disease): Results from a prospective, multicenter study over 66 weeks</title>
            <link>http://www.medworm.com/index.php?rid=5562003&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24889</link>
            <description>AbstractThe purpose of this study was to evaluate the incidence of augmentation over 66 weeks of treatment with ropinirole in patients with primary restless legs syndrome (RLS). Augmentation is the main complication of long‐term dopaminergic treatment of RLS. Despite widespread use of ropinirole in RLS, no studies have prospectively and systematically assessed the incidence of augmentation with its use. The study consisted of 26 weeks of double‐blind flexible‐dose treatment with ropinirole or placebo, followed by 40 weeks of open‐label ropinirole treatment.. Patients had no previous history of augmentation. Potential cases of augmentation were identified with the Structured Interview for the Diagnosis of Augmentation and the Augmentation Severity Rating Scale and through reporting ...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5562003</comments>
            <pubDate>Wed, 04 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5562003</guid>        </item>
        <item>
            <title>Investigating visual misperceptions in Parkinson's disease: A novel behavioral paradigm</title>
            <link>http://www.medworm.com/index.php?rid=5562002&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24900</link>
            <description>AbstractVisual misperception and hallucinations represent a major problem in advanced PD. The pathophysiological mechanisms underlying these symptoms remain poorly understood, with limited tests for their assessment. A recent hypothesis has suggested that visual misperception and hallucinations may arise from disrupted processing in the attentional networks. To assess and quantify visual misperceptions, we developed the novel bistable percept paradigm (BPP), which consists of a battery of “single” and “hidden” monochromatic images that subjects are required to study until they are satisfied that they have recognized everything that the image may represent. In this experiment, 45 patients and 18 age‐matched controls performed the BPP. Using an error score value derived from the co...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5562002</comments>
            <pubDate>Wed, 04 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5562002</guid>        </item>
        <item>
            <title>The association between Mediterranean diet adherence and Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5668708&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24918</link>
            <description>Conclusions:PD patients adhere less than controls to a Mediterranean‐type diet. Dietary behavior may be associated with age at onset. © 2012 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5668708</comments>
            <pubDate>Sun, 01 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5668708</guid>        </item>
        <item>
            <title>Pseudo‐heterozygous rearrangement mutation of parkin</title>
            <link>http://www.medworm.com/index.php?rid=5660904&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24906</link>
            <description>Conclusions:For correct determination of rearrangement mutation, mutation analysis of the patient as well as other family members and/or break‐point analysis of genomic DNA and at the transcript level should be conducted. © 2012 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5660904</comments>
            <pubDate>Sun, 01 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5660904</guid>        </item>
        <item>
            <title>Significance and usefulness of heart rate variability in patients with multiple system atrophy</title>
            <link>http://www.medworm.com/index.php?rid=5650096&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24929</link>
            <description>Conclusions:The cardiac autonomic state of multiple system atrophy was characterized by decreases in both sympathetic and parasympathetic tones. Because heart rate variability parameters were not affected by other autonomic dysfunctions, this may be a useful method for evaluating cardiac autonomic dysfunction in multiple system atrophy. © 2012 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650096</comments>
            <pubDate>Sun, 01 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650096</guid>        </item>
        <item>
            <title>Trichophagia affects response to duodenal levodopa/carbidopa gel administration</title>
            <link>http://www.medworm.com/index.php?rid=5639518&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24898</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639518</comments>
            <pubDate>Sun, 01 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5639518</guid>        </item>
        <item>
            <title>The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5630531&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24927</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5630531</comments>
            <pubDate>Sun, 01 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5630531</guid>        </item>
        <item>
            <title>Subthalamic nucleus neuronal firing rates in Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5611150&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24901</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611150</comments>
            <pubDate>Sun, 01 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611150</guid>        </item>
        <item>
            <title>Progressive ataxia with palatal tremor due to gluten sensitivity</title>
            <link>http://www.medworm.com/index.php?rid=5599404&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23987</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5599404</comments>
            <pubDate>Sun, 01 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5599404</guid>        </item>
        <item>
            <title>Functional connectivity in human and monkey brain: New insights for understanding movement disorders?</title>
            <link>http://www.medworm.com/index.php?rid=5599403&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24063</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5599403</comments>
            <pubDate>Sun, 01 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5599403</guid>        </item>
        <item>
            <title>Toward a redefinition of Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5599402&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24051</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5599402</comments>
            <pubDate>Sun, 01 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5599402</guid>        </item>
        <item>
            <title>Dreaming in dementia—REM sleep behavior disorder and synucleinopathy</title>
            <link>http://www.medworm.com/index.php?rid=5599401&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24047</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5599401</comments>
            <pubDate>Sun, 01 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5599401</guid>        </item>
        <item>
            <title>Can imaging separate multiple system atrophy from Parkinson's disease?</title>
            <link>http://www.medworm.com/index.php?rid=5599400&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24046</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5599400</comments>
            <pubDate>Sun, 01 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5599400</guid>        </item>
        <item>
            <title>Locus coeruleus dysfunction: A feature of essential or senile tremor?</title>
            <link>http://www.medworm.com/index.php?rid=5599399&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24885</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5599399</comments>
            <pubDate>Sun, 01 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5599399</guid>        </item>
        <item>
            <title>Huntington's disease: Objective assessment of posture—A link between motor and functional deficits</title>
            <link>http://www.medworm.com/index.php?rid=5599393&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24908</link>
            <description>Conclusions:Posturography may provide useful objective and quantitative measures of postural motor dysfunction in Huntington's disease. © 2012 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5599393</comments>
            <pubDate>Sun, 01 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5599393</guid>        </item>
        <item>
            <title>Subthalamic neuronal responses to cortical stimulation</title>
            <link>http://www.medworm.com/index.php?rid=5553301&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24053</link>
            <description>Conclusions:To prevent seizures the current density should be lowered, so that motor cortex stimulation‐evoked responses can be safely used during deep brain stimulation surgery. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5553301</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5553301</guid>        </item>
        <item>
            <title>Comparison of office‐based versus home web‐based clinical assessments for Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5506761&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24028</link>
            <description>Conclusions:Web‐based assessments offer a feasible format for assessing PD‐related impairment from home. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506761</comments>
            <pubDate>Thu, 15 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506761</guid>        </item>
        <item>
            <title>Eye symptoms in relatives of patients with primary adult‐onset dystonia</title>
            <link>http://www.medworm.com/index.php?rid=5506760&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24026</link>
            <description>Conclusions:Eye symptoms reported by relatives of patients with focal dystonia probably result from eye diseases and are not part of the clinical spectrum of blepharospasm. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506760</comments>
            <pubDate>Thu, 15 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506760</guid>        </item>
        <item>
            <title>Bilateral deep brain stimulation for cervical dystonia in patients with previous peripheral surgery</title>
            <link>http://www.medworm.com/index.php?rid=5506759&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24022</link>
            <description>Conclusions:Patients who had prior peripheral surgery for cervical dystonia experience improvement from subsequent pallidal stimulation that is comparable to that of de novo patients. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506759</comments>
            <pubDate>Thu, 15 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506759</guid>        </item>
        <item>
            <title>Narrowing wide‐field optic flow affects treadmill gait in left‐sided Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5506758&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24011</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506758</comments>
            <pubDate>Thu, 15 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506758</guid>        </item>
        <item>
            <title>Dissociating between sensory and perceptual deficits in PD: More than simply a motor deficit</title>
            <link>http://www.medworm.com/index.php?rid=5506757&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24042</link>
            <description>AbstractAlthough Parkinson's disease (PD) is traditionally considered a motor output disorder, recent evidence suggests that people with PD may have sensory and perceptual impairments that may underlie movement impairments. Yet there has not been any direct testing of perceptual judgments, especially when manipulating the sensory feedback on which these judgments are made. The present study investigated how perception might be influenced by sensory feedback to contribute to height estimations and obstacle stepping in PD relative to healthy age‐matched control participants. Perceptual judgment accuracy was evaluated by judging 3 typically encountered obstacle heights in 2 sensory feedback conditions: (1) vision of foot available and (2) without vision of foot (reliance on proprioceptive f...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506757</comments>
            <pubDate>Thu, 15 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506757</guid>        </item>
        <item>
            <title>Age, CAG repeat length, and clinical progression in Huntington's disease</title>
            <link>http://www.medworm.com/index.php?rid=5506756&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24024</link>
            <description>The objective of this study was to further explore the effect of CAG repeat length on the rate of clinical progression in patients with Huntington's disease. The dataset included records for 569 subjects followed prospectively at the Baltimore Huntington's Disease Center. Participants were seen for a mean of 7.1 visits, with a mean follow‐up of 8.2 years. Subjects were evaluated using the Quantified Neurologic Examination and its Motor Impairment subscale, the Mini‐Mental State Examination, and the Huntington's disease Activities of Daily Living Scale. By itself, CAG repeat length showed a statistically significant but small effect on the progression of all clinical measures. Contrary to our previous expectations, controlling for age of onset increased the correlation between CAG repea...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506756</comments>
            <pubDate>Thu, 15 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506756</guid>        </item>
        <item>
            <title>Unilateral basal ganglia atrophy in a patient with tuberous sclerosis complex and hemichorea</title>
            <link>http://www.medworm.com/index.php?rid=5506755&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24014</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506755</comments>
            <pubDate>Thu, 15 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506755</guid>        </item>
        <item>
            <title>A “twist in the tale”: Altered perception of ankle position in psychogenic dystonia</title>
            <link>http://www.medworm.com/index.php?rid=5506754&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24069</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506754</comments>
            <pubDate>Thu, 15 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506754</guid>        </item>
        <item>
            <title>A motor signature of REM sleep behavior disorder</title>
            <link>http://www.medworm.com/index.php?rid=5506753&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24044</link>
            <description>Conclusions:These characteristics of movements were found in the 3 conditions (Parkinson's disease, idiopathic RBD, and primary narcolepsy), delineating a common motor signature of RBD. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506753</comments>
            <pubDate>Thu, 15 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506753</guid>        </item>
        <item>
            <title>Fragile X–Associated tremor ataxia syndrome in FMR1 gray zone allele carriers</title>
            <link>http://www.medworm.com/index.php?rid=5495972&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24021</link>
            <description>Conclusions:Our cases suggest that the definition of the FXTAS may need to be broadened to include individuals with FMR1 repeat expansions in the gray zone. These neurological signs may be due to elevated levels of expanded CGG repeat FMR1 mRNA in the gray zone carriers, similar to the changes seen in premutation carriers with FXTAS. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5495972</comments>
            <pubDate>Sun, 11 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5495972</guid>        </item>
        <item>
            <title>Placebo effect characteristics observed in a single, international, longitudinal study in Huntington's disease</title>
            <link>http://www.medworm.com/index.php?rid=5488524&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24062</link>
            <description>Conclusions:In Huntington's disease, behavior seems to be more vulnerable to placebo than overall motor function, cognition, and function © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488524</comments>
            <pubDate>Fri, 09 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5488524</guid>        </item>
        <item>
            <title>Intergenerational instability in Huntington disease: Extreme repeat changes among 134 transmissions</title>
            <link>http://www.medworm.com/index.php?rid=5488523&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24065</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488523</comments>
            <pubDate>Fri, 09 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5488523</guid>        </item>
        <item>
            <title>Parkinson's disease patients cannot get their dopamine replacement: The 8‐sinemet limit</title>
            <link>http://www.medworm.com/index.php?rid=5488522&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24038</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488522</comments>
            <pubDate>Fri, 09 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5488522</guid>        </item>
        <item>
            <title>Perampanel, an AMPA antagonist, Found to have no benefit in reducing “Off” time in Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5488521&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23983</link>
            <description>Conclusions:Perampanel failed to significantly improve motor symptoms versus placebo. There was also no effect on the duration or disability of levodopa‐induced dyskinesia. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488521</comments>
            <pubDate>Fri, 09 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5488521</guid>        </item>
        <item>
            <title>Substantia nigra hypoechogenicity in friedreich ataxia</title>
            <link>http://www.medworm.com/index.php?rid=5488520&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23989</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488520</comments>
            <pubDate>Fri, 09 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5488520</guid>        </item>
        <item>
            <title>Emotional processing in Parkinson's disease: A systematic review</title>
            <link>http://www.medworm.com/index.php?rid=5488519&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24025</link>
            <description>AbstractParkinson's disease provides a useful model for studying the neural substrates of emotional processing. The striato‐thalamo‐cortical circuits, like the mesolimbic dopamine system that modulates their function, are thought to be involved in emotional processing. As Parkinson's disease is histopathologically characterized by the selective, progressive, and chronic degeneration of the nigrostriatal and mesocorticolimbic dopamine systems, it can therefore serve as a model for assessing the functional role of these circuits in humans. In the present review, we begin by providing a synopsis of the emotional disturbances observed in Parkinson's disease. We then discuss the functional roles of the striato‐thalamo‐cortical and mesolimbic circuits, ending with the conclusion that bot...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488519</comments>
            <pubDate>Fri, 09 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5488519</guid>        </item>
        <item>
            <title>A Korean Parkinson's disease family with the LRRK2 p.Tyr1699Cys mutation showing clinical heterogeneity</title>
            <link>http://www.medworm.com/index.php?rid=5488518&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24033</link>
            <description>Conclusions:This is the first report describing an Asian PD family with the p.Tyr1699Cys mutation in LRRK2. The affected members of this family showed clinical heterogeneity. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488518</comments>
            <pubDate>Fri, 09 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5488518</guid>        </item>
        <item>
            <title>Diffusion tensor imaging of freezing of gait in patients with white matter changes</title>
            <link>http://www.medworm.com/index.php?rid=5488517&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24034</link>
            <description>Conclusions:Our findings suggest that the bilateral pedunculopontine nucleus, bilateral superior premotor cortex, right orbitofrontal area, and left supplement motor area are closely related to freezing of gait. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488517</comments>
            <pubDate>Fri, 09 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5488517</guid>        </item>
        <item>
            <title>Evaluation of periodic limb movements in a putative animal model of restless leg syndrome</title>
            <link>http://www.medworm.com/index.php?rid=5488516&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24058</link>
            <description>AbstractRestless leg syndrome (RLS) is a major healthcare burden with increasing prevalence. It has been demonstrated that periodic limb movements (PLM) can occur as an isolated phenomenon, but they are often associated with this syndrome and are the only symptom of this disorder that can be measured electrophysiologically. The aim of this study was to examine the sleep‐wake behavior and the presence of limb movement in a rat model of RLS induced by lesioning the A11 dopaminergic nuclei with the neurotoxin 6‐hydroxydopamine (6‐OHDA). Rats were implanted with electrodes for electrocorticography and electromyography. Sleep recordings were monitored during light/dark periods lasting 12 hours each and were evaluated on days 7, 15, and 28 after injection of the drug or phosphate‐buffere...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488516</comments>
            <pubDate>Fri, 09 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5488516</guid>        </item>
        <item>
            <title>Clinical validation of movement disorder society–recommended diagnostic criteria for Parkinson's disease with dementia</title>
            <link>http://www.medworm.com/index.php?rid=5488515&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24059</link>
            <description>The objective of this work was to evaluate the Movement Disorders Society (MDS) Task Force–proposed screening checklist for detecting Parkinson's disease dementia (PD‐D) in relation to full neuropsychological testing. An MDS Task Force has proposed diagnostic procedures for PD‐D, which have not been fully validated against more extensive neuropsychological testing. PD subjects were recruited from 2 specialty centers. A neuropsychologist evaluated them for dementia as part of routine clinical care. Independent clinical neurologists administered the MDS PD‐D screening checklist. Diagnosis of PD‐D by the 2 methods was compared. Ninety‐one PD subjects had a mean age of 66.3 (SD = 9.7) years and a mean PD duration of 8.8 (SD = 6.1) years. Seven subjects (7.7%) met all 8 screening ch...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488515</comments>
            <pubDate>Fri, 09 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5488515</guid>        </item>
        <item>
            <title>Stereotypies: A critical appraisal and suggestion of a clinically useful definition</title>
            <link>http://www.medworm.com/index.php?rid=5488514&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23994</link>
            <description>AbstractThe foundations of the clinical classification of movement disorders rest on the precise definition of the words used to describe the disorders. Here we argue that the current use of the term stereotypy falls well short of the precision needed for either clinical or academic use, and fails both to provide a clinically useful diagnostic category and to define a set of conditions that are linked pathophysiologically. The difficulty in defining this concept is not a new one as our review of the history of the term demonstrates. We synthesise this historical background, explore why clinicians have felt it necessary to use the category of stereotypy for certain movements rather than the related category of tics, discuss the multiple uses of the term in current research and clinical prac...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488514</comments>
            <pubDate>Fri, 09 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5488514</guid>        </item>
        <item>
            <title>Interesting complication of the Medtronic Activa RC impulse pulse generator</title>
            <link>http://www.medworm.com/index.php?rid=5561998&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24019</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5561998</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5561998</guid>        </item>
        <item>
            <title>25‐hydroxyvitamin D, vitamin D receptor gene polymorphisms, and severity of Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5553300&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24016</link>
            <description>AbstractWe aimed to examine associations among serum 25‐hydroxyvitamin D levels, 1,25‐dihyroxyvitamin D levels, vitamin D receptor polymorphisms, vitamin D binding protein gene polymorphisms, and the severity of Parkinson's disease. In 137 patients, the severity of Parkinson's disease was evaluated using Hoehn &amp; Yahr stage and Unified Parkinson's Disease Rating Stage by neurologists and compared with 25‐hydroxyvitamin D, 1,25‐hydroxyvitamin D, vitamin D receptor polymorphisms, ie, FokI (rs10735810), BsmI (rs1544410), Cdx2 (rs11568820), ApaI (rs7976091), and TaqI (rs731236), and vitamin D binding protein gene polymorphisms GC1 (rs7041)/GC2 (rs4588) in a cross‐sectional study. Mean ± standard deviation levels of 25‐hydroxyvitamin D were 21.1 ± 9.0 ng/mL. Levels were deficie...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5553300</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5553300</guid>        </item>
        <item>
            <title>Apathy in essential tremor, dystonia, and parkinson's disease: A comparison with normal controls</title>
            <link>http://www.medworm.com/index.php?rid=5526969&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24049</link>
            <description>Conclusions:Patients with Parkinson's disease, essential tremor, and dystonia had elevated apathy scores. Features of apathy seemed to occur in these conditions independent of depressive symptoms. The mechanistic basis for the apparent increased features of apathy in essential tremor and dystonia deserves further study. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5526969</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5526969</guid>        </item>
        <item>
            <title>Erratum</title>
            <link>http://www.medworm.com/index.php?rid=5506774&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24043</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506774</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506774</guid>        </item>
        <item>
            <title>Reply: Rapidly progressing diffuse Lewy body disease</title>
            <link>http://www.medworm.com/index.php?rid=5506773&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23981</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506773</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506773</guid>        </item>
        <item>
            <title>Pluripotent stem cells with triplication of alpha‐synuclein locus</title>
            <link>http://www.medworm.com/index.php?rid=5506772&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24056</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506772</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506772</guid>        </item>
        <item>
            <title>Metabotropic glutamate receptors—mGluR5—new kid on the dissecting block?</title>
            <link>http://www.medworm.com/index.php?rid=5506771&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24057</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506771</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506771</guid>        </item>
        <item>
            <title>The Wilson films — Sydenham Chorea</title>
            <link>http://www.medworm.com/index.php?rid=5506770&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24032</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506770</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506770</guid>        </item>
        <item>
            <title>The Wilson films — Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5506769&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24031</link>
            <description>AbstractShort sequences in the Wilson film illustrate clinical aspects of bradykinesia and tremor in Parkinson's disease. What might have been the motivation of Wilson to capture these symptoms, and how would we view them today? © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506769</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506769</guid>        </item>
        <item>
            <title>The Wilson films — Wilson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5506768&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24037</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506768</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506768</guid>        </item>
        <item>
            <title>The Wilson films — MS Tremor</title>
            <link>http://www.medworm.com/index.php?rid=5506767&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24010</link>
            <description>AbstractAction tremor was for a long time considered to be a defining symptom of multiple sclerosis. The Wilson films include a short segment showing a female patient suffering from relatively severe action tremor. Tremor is the most common movement disorder in multiple sclerosis, and can be very disabling in some patients. Insights into the frequency and treatment of tremor in multiple sclerosis have changed since the Wilson films were taken, and are reviewed herein. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506767</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506767</guid>        </item>
        <item>
            <title>The Wilson films — Hemiballism</title>
            <link>http://www.medworm.com/index.php?rid=5506766&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23995</link>
            <description>AbstractThe case presented involves an 88‐year‐old woman with sudden onset of right‐sided hemiballism that persisted for an amazing 15 years. The video demonstrates wide amplitude choreic movements of the proximal and distal limbs of the right side, as well as of the axial musculature. Classical teaching dictates that this patient has a lesion in the subthalamic nucleus. Here then is a prime example where classical teaching is wrong! © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506766</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506766</guid>        </item>
        <item>
            <title>The Wilson films — Psychogenic</title>
            <link>http://www.medworm.com/index.php?rid=5506765&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23992</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506765</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506765</guid>        </item>
        <item>
            <title>The Wilson films — Huntington's Chorea</title>
            <link>http://www.medworm.com/index.php?rid=5506764&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23986</link>
            <description>AbstractWilson's Queen Square Case 9 with Huntington's chorea shows a 68‐year‐old man with mild to moderate generalized chorea, impaired fixation, and probable cognitive decline in keeping with a diagnosis of Huntington's disease (HD). An age of onset in the late sixties and a negative family history suggest a relatively small expanded trinucleotide repeat in the HTT gene in the patient and reduced penetrance of an even shorter repeat allele in one of his parents. A highly sensitive and specific gene test has been offered worldwide for diagnostic testing of HD for almost two decades. This test, obviously unavailable at Wilson's times, became the historic frontrunner for guidelines of symptomatic, presymptomatic, and prenatal testing for an adult‐onset neurodegenerative disorder. Rega...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506764</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506764</guid>        </item>
        <item>
            <title>The Wilson films — Bilateral postural tremor</title>
            <link>http://www.medworm.com/index.php?rid=5506763&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23927</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506763</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506763</guid>        </item>
        <item>
            <title>Commentary on the postencephalitic cases of Dr. Kinnier Wilson</title>
            <link>http://www.medworm.com/index.php?rid=5506762&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23900</link>
            <description>AbstractThree cases of postencephalitic parkinsonism that were originally described by Kinnier Wilson are reviewed and some general comments made upon their presentation. A differential diagnosis that might now be appropriate in the 21st Century is given, in the light of recent literature on the topic and so‐called “sporadic” cases. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506762</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506762</guid>        </item>
        <item>
            <title>Glucocerebrosidase mutations confer a greater risk of dementia during Parkinson's disease course</title>
            <link>http://www.medworm.com/index.php?rid=5506752&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24045</link>
            <description>AbstractMutations in the glucocerebrosidase gene are associated with Parkinson's disease and Lewy body dementia. However, whether these alterations have any effect on the clinical course of Parkinson's disease is not clear. The glucocerebrosidase coding region was fully sequenced in 225 Parkinson's disease patients, 17 pathologically confirmed Lewy body dementia patients, and 186 controls from Spain. Twenty‐two Parkinson's disease patients (9.8%) and 2 Lewy body dementia patients (11.8%) carried mutations in the glucocerebrosidase gene, compared with only 1 control (0.5%); P = .016 and P = .021 for Parkinson's disease and Lewy body dementia, respectively. The N370S and the L444P mutations represented 50% of the alterations. Two novel variants, L144V and S488T, and 7 previously described ...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506752</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506752</guid>        </item>
        <item>
            <title>Hand bradykinesia improved by DBS in the dorsal putamen?</title>
            <link>http://www.medworm.com/index.php?rid=5470275&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24001</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5470275</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5470275</guid>        </item>
        <item>
            <title>High‐frequency deep brain stimulation of the putamen improves bradykinesia in Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5442987&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23998</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5442987</comments>
            <pubDate>Wed, 23 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5442987</guid>        </item>
        <item>
            <title>Instability of syllable repetition in patients with spinocerebellar ataxia and Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5442989&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24030</link>
            <description>Conclusions:Cerebellar function may be required for the general precision of interval timing, whereas basal ganglia rather serve to maintain rhythm stability over time. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5442989</comments>
            <pubDate>Tue, 22 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5442989</guid>        </item>
        <item>
            <title>G303V tau mutation presenting with progressive supranuclear palsy–like features</title>
            <link>http://www.medworm.com/index.php?rid=5442988&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24060</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5442988</comments>
            <pubDate>Tue, 22 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5442988</guid>        </item>
        <item>
            <title>Dopamine transporter imaging in autopsy‐confirmed Parkinson's disease and multiple system atrophy</title>
            <link>http://www.medworm.com/index.php?rid=5423728&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24000</link>
            <description>AbstractDopamine transporter single‐photon emission computerized tomography can visualize dopaminergic degeneration in Parkinson's disease and multiple system atrophy. Some studies have suggested that dopamine transporter imaging can distinguish these disorders based on a more diffuse and symmetric striatal dopamine transporter binding loss in multiple system atrophy. The present study compared patterns of striatal dopamine transporter distribution in postmortem‐confirmed Parkinson's disease and multiple system atrophy. Patients with a postmortem diagnosis of multiple system atrophy (n = 6) or Parkinson's disease (n = 8) who had undergone dopamine transporter imaging were included. Imaging had been performed after a mean disease duration of 3.6 and 4.1 years in multiple system atrophy ...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5423728</comments>
            <pubDate>Fri, 18 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5423728</guid>        </item>
        <item>
            <title>Rate of change in early Huntington's disease: A clinicometric analysis</title>
            <link>http://www.medworm.com/index.php?rid=5423730&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23847</link>
            <description>AbstractSensitive outcome measures for patients with Huntington's disease (HD) are required for future clinical trials. Longitudinal data were collected from a 3‐year study of 379 patients suffering from early HD who were not treated by antipsychotics. Progression of UHDRS item scores was evaluated by linear regression and slope, whereas correlation coefficient, standard error, and P values were estimated on the basis of the data of eight evaluations from screening to study end (36 months). For the functional assessment dimension, the proportion of “no” responses at baseline and at study end was determined. Linear progression was observed for the motor score and for all three functional measures (i.e., functional assessment score, independence assessment score, and total functional c...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5423730</comments>
            <pubDate>Thu, 17 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5423730</guid>        </item>
        <item>
            <title>Breathing instability in joubert syndrome</title>
            <link>http://www.medworm.com/index.php?rid=5423729&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23999</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5423729</comments>
            <pubDate>Thu, 17 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5423729</guid>        </item>
        <item>
            <title>The normal parkin sequence</title>
            <link>http://www.medworm.com/index.php?rid=5410466&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24050</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410466</comments>
            <pubDate>Wed, 16 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5410466</guid>        </item>
        <item>
            <title>Catechol‐O‐methyltransferase Val158Met and the risk of dyskinesias in Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5410468&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23805</link>
            <description>Conclusions:This finding suggests that genetic factors may affect susceptibility to dyskinesias in PD. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410468</comments>
            <pubDate>Mon, 14 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5410468</guid>        </item>
        <item>
            <title>Dentatorubral‐pallidoluysian atrophy: Haplotype of Asian origin in 2 Italian families</title>
            <link>http://www.medworm.com/index.php?rid=5410467&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24027</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410467</comments>
            <pubDate>Mon, 14 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5410467</guid>        </item>
        <item>
            <title>Annual change in Friedreich's ataxia evaluated by the scale for the assessment and rating of ataxia (SARA) is independent of disease severity</title>
            <link>http://www.medworm.com/index.php?rid=5401671&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23879</link>
            <description>Conclusions:In adult Friedreich's ataxia patients the Scale for the Assessment and Rating of Ataxia can detect annual changes independently of disease severity. In future therapeutic trials no patient stratification is globally required. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5401671</comments>
            <pubDate>Thu, 10 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5401671</guid>        </item>
        <item>
            <title>Do levodopa treatments modify the morphology of the parkinsonian brain?</title>
            <link>http://www.medworm.com/index.php?rid=5401670&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24018</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5401670</comments>
            <pubDate>Thu, 10 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5401670</guid>        </item>
        <item>
            <title>Prefrontal alterations in Parkinson's disease with levodopa‐induced dyskinesia during fMRI motor task</title>
            <link>http://www.medworm.com/index.php?rid=5401669&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24017</link>
            <description>In this study, the functional relevance of this structural abnormality was explored using functional magnetic resonance imaging. Ten dyskinetic PD patients and 10 nondyskinetic PD patients were studied in the OFF phase with functional magnetic resonance imaging while performing externally and internally triggered visuomotor tasks. Although neither group demonstrated behavioral differences during execution of motor tasks, magnetic resonance imaging analysis detected significant changes in target cortical regions. In particular, PD patients with levodopa‐induced dyskinesia showed significant overactivity in the supplementary motor area and underactivity in the right inferior prefrontal gyrus during execution of both tasks when compared with PD patients without levodopa‐induced dyskinesia...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5401669</comments>
            <pubDate>Thu, 10 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5401669</guid>        </item>
        <item>
            <title>Parkinson's disease motor subtypes and mood</title>
            <link>http://www.medworm.com/index.php?rid=5495971&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24041</link>
            <description>AbstractParkinson's disease is heterogeneous, both in terms of motor symptoms and mood. Identifying associations between phenotypic variants of motor and mood subtypes may provide clues to understand mechanisms underlying mood disorder and symptoms in Parkinson's disease. A total of 513 patients were assessed using the Hospital Anxiety and Depression Scale, and separately classified into anxious, depressed, and anxious‐depressed mood classes based on latent class analysis of a semistructured interview. Motor subtypes assessed related to age‐of‐onset, rate of progression, presence of motor fluctuations, lateralization of motor symptoms, tremor dominance, and the presence of postural instability and gait symptoms and falls. The directions of observed associations tended to support prev...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5495971</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5495971</guid>        </item>
        <item>
            <title>Severe dysphagia as a presentation of Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5488513&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24006</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5488513</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5488513</guid>        </item>
        <item>
            <title>Questionnaire for impulsive‐compulsive disorders in Parkinson's Disease–Rating Scale</title>
            <link>http://www.medworm.com/index.php?rid=5470274&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24023</link>
            <description>AbstractImpulse control disorders and related disorders (hobbyism‐punding and dopamine dysregulation syndrome) occur in 15% to 20% of Parkinson's disease (PD) patients. We assessed the validity and reliability of the Questionnaire for Impulsive‐Compulsive Disorders in Parkinson's Disease–Rating Scale (QUIP‐RS), a rating scale designed to measure severity of symptoms and support a diagnosis of impulse control disorders and related disorders in PD. A convenience sample of PD patients at a movement disorders clinic self‐completed the QUIP‐RS and were administered a semistructured diagnostic interview by a blinded trained rater to assess discriminant validity for impulse control disorders (n = 104) and related disorders (n = 77). Subsets of patients were assessed to determine inter...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5470274</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5470274</guid>        </item>
        <item>
            <title>CAG repeat size in the normal HTT allele and age of onset in Huntington's disease</title>
            <link>http://www.medworm.com/index.php?rid=5442993&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23849</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5442993</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5442993</guid>        </item>
        <item>
            <title>Hemifacial spasm associated with intraparenchymal brain stem tumor</title>
            <link>http://www.medworm.com/index.php?rid=5442992&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23877</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5442992</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5442992</guid>        </item>
        <item>
            <title>The true nature of α‐synuclein unmasked!</title>
            <link>http://www.medworm.com/index.php?rid=5442991&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24009</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5442991</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5442991</guid>        </item>
        <item>
            <title>Deep brain stimulation for Parkinson's disease: Thinking about the long‐term in the short‐term</title>
            <link>http://www.medworm.com/index.php?rid=5442990&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24036</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5442990</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5442990</guid>        </item>
        <item>
            <title>Alleviation of dysphagia after deep brain stimulation: results from a Parkinson's disease patient</title>
            <link>http://www.medworm.com/index.php?rid=5442986&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23899</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5442986</comments>
            <pubDate>Tue, 01 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5442986</guid>        </item>
        <item>
            <title>Sensory sensitivity to external stimuli in Tourette syndrome patients</title>
            <link>http://www.medworm.com/index.php?rid=5365453&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23977</link>
            <description>In this study (1) we defined the patients' experience of sensitivity to external stimuli in detail, and (2) we tested 2 hypotheses regarding its origin. First, we interviewed in depth and administered a lengthy questionnaire to adult Tourette patients (n = 19) and age‐matched healthy volunteers (n = 19). Eighty percent of patients described heightened sensitivity to external stimuli, with examples among all 5 sensory modalities. Bothersome stimuli were characterized as faint, repetitive or constant, and nonsalient, whereas intense stimuli were well tolerated. We then determined whether the sensitivity could be the result of an increased ability to detect faint stimuli. After measuring the threshold of detection for olfactory and tactile stimuli among the patients and healthy volunteers, ...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5365453</comments>
            <pubDate>Fri, 28 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5365453</guid>        </item>
        <item>
            <title>LRRK2 haplotype‐sharing analysis in Parkinson's disease reveals a novel p.S1761R mutation</title>
            <link>http://www.medworm.com/index.php?rid=5365452&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23968</link>
            <description>AbstractBackground and objective.Mutations in the Leucine‐Rich Repeat Kinase 2 (LRRK2) gene at chromosome 12q12 are the most common genetic cause of sporadic and familial late‐onset Parkinson's disease. Our aim was to identify novel LRRK2 mutations in late‐onset Parkinson's disease families.Design.We analyzed chromosome 12p11.2‐q13.1 haplotypes in 14 late‐onset Parkinson's disease families without known LRRK2 mutations.Results.Haplotype analysis identified 12 families in which the affected subjects shared chromosome 12p11.2‐q13.1 haplotypes. LRRK2 sequencing revealed a novel co‐segregating missense mutation in exon 36 (c.5281A&amp;gt;C; p.S1761R) located within a highly conserved region of the COR [C‐terminal of ROC (Ras of complex proteins)] domain wherein it could deregulate ...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5365452</comments>
            <pubDate>Fri, 28 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5365452</guid>        </item>
        <item>
            <title>Genetic diagnosis of neuroacanthocytosis disorders using exome sequencing</title>
            <link>http://www.medworm.com/index.php?rid=5365451&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24020</link>
            <description>Conclusions:Exome sequencing is a valuable diagnostic tool in the neuroacanthocytosis syndromes. These studies may provide a better understanding of the function of the associated proteins and provide insight into the pathogenesis of these disorders. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5365451</comments>
            <pubDate>Fri, 28 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5365451</guid>        </item>
        <item>
            <title>Brain biochemistry in autopsied patients with essential tremor</title>
            <link>http://www.medworm.com/index.php?rid=5365450&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24004</link>
            <description>AbstractThe pathology of essential tremor is increasingly being studied; however, there are limited studies of biochemical changes in this condition. We studied several candidate biochemical/anatomical systems in the brain stem, striatum, and cerebellum of 23 essential tremor subjects who came to autopsy, comparing them with a control population. Striatal tyrosine hydroxylase, a marker of dopaminergic neurons, was 91.7 ± 113.2 versus 96.4 ± 102.7 ng/mg (not significant) in cases and controls, respectively. Locus coeruleus dopamine beta‐hydroxylase, a marker of noradrenergic neurons, was not significantly different between the essential tremor and control groups. Parvalbumin, a marker of GABAergic neurons, was 199.3 ± 42.0 versus 251.4 ± 74.8 ng/mg (P = .025) in the pons in the region...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5365450</comments>
            <pubDate>Fri, 28 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5365450</guid>        </item>
        <item>
            <title>Rapid eye movement sleep behavior disorder and subtypes in autopsy‐confirmed dementia with Lewy bodies</title>
            <link>http://www.medworm.com/index.php?rid=5365449&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24003</link>
            <description>AbstractThe purpose of this study was to determine whether dementia with Lewy bodies with and without probable rapid eye movement sleep behavior disorder differ clinically or pathologically. Patients with dementia with Lewy bodies (DLB) with probable rapid eye movement sleep behavior sleep disorder (n = 71) were compared with those without it (n = 19) on demographics, clinical variables (core features of dementia with Lewy bodies, dementia duration, rate of cognitive/motor changes), and pathologic indices (Lewy body distribution, neuritic plaque score, Braak neurofibrillary tangle stage). Individuals with probable rapid eye movement sleep behavior disorder were predominantly male (82% vs 47%) and had a shorter duration of dementia (mean, 8 vs 10 years), earlier onset of parkinsonism (mean,...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5365449</comments>
            <pubDate>Fri, 28 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5365449</guid>        </item>
        <item>
            <title>Rapidly progressing diffuse Lewy body disease</title>
            <link>http://www.medworm.com/index.php?rid=5365448&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23976</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5365448</comments>
            <pubDate>Fri, 28 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5365448</guid>        </item>
        <item>
            <title>Serum levels of N‐acetylaspartate in Huntington's disease: Preliminary results</title>
            <link>http://www.medworm.com/index.php?rid=5365447&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23974</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5365447</comments>
            <pubDate>Fri, 28 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5365447</guid>        </item>
        <item>
            <title>Hemimasticatory spasm following surgery for vestibular schwannoma</title>
            <link>http://www.medworm.com/index.php?rid=5349726&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23988</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5349726</comments>
            <pubDate>Mon, 24 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5349726</guid>        </item>
        <item>
            <title>Attention to self in psychogenic tremor</title>
            <link>http://www.medworm.com/index.php?rid=5349725&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23911</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5349725</comments>
            <pubDate>Mon, 24 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5349725</guid>        </item>
        <item>
            <title>Dopamine dysregulation syndrome item from the MDS‐UPDRS</title>
            <link>http://www.medworm.com/index.php?rid=5349724&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23910</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5349724</comments>
            <pubDate>Mon, 24 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5349724</guid>        </item>
        <item>
            <title>Genetic variants of α‐synuclein are not associated with essential tremor</title>
            <link>http://www.medworm.com/index.php?rid=5349723&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23909</link>
            <description>Conclusions:Whereas genetic factors are likely to play a large role in essential tremor pathogenesis, our results do not support a role for common SNCA genetic variants in risk for essential tremor. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5349723</comments>
            <pubDate>Mon, 24 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5349723</guid>        </item>
        <item>
            <title>A proof‐of‐concept trial of the whey protein alfa‐lactalbumin in chronic cortical myoclonus</title>
            <link>http://www.medworm.com/index.php?rid=5349722&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23908</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5349722</comments>
            <pubDate>Mon, 24 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5349722</guid>        </item>
        <item>
            <title>Freezing in Parkinson's disease: A spatiotemporal motor disorder beyond gait</title>
            <link>http://www.medworm.com/index.php?rid=5338150&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24015</link>
            <description>AbstractFreezing of gait (FOG) is an incapacitating problem in Parkinson's disease that is difficult to manage therapeutically. We tested the hypothesis that impaired rhythm and amplitude control is a common mechanism of freezing which is also present during other rhythmic tasks. Therefore, we compared the occurrence and spatiotemporal profiles of freezing episodes during upper limb motion, lower limb motion, and FOG. Eleven freezers, 12 non‐freezers, and 11 controls performed a rhythmic bilateral finger movement task. The triggering effect of movement speed, amplitude, and coordination pattern was evaluated. Regression slopes and spectral analysis addressed the spatial and temporal kinematic changes inherent to freezing episodes. The FOG Questionnaire score significantly predicted sever...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5338150</comments>
            <pubDate>Fri, 21 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5338150</guid>        </item>
        <item>
            <title>Doorway‐provoked freezing of gait in Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5316891&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23990</link>
            <description>AbstractFreezing of gait in Parkinson's disease can be difficult to study in the laboratory. Here we investigate the use of a variable‐width doorway to provoke freeze behavior together with new objective methods to measure it. With this approach we compare the effects of anti‐parkinsonian treatments (medications and deep‐brain stimulation of the subthalamic nucleus) on freezing and other gait impairments. Ten “freezers” and 10 control participants were studied. Whole‐body kinematics were measured while participants walked at preferred speed in each of 4 doorway conditions (no door present, door width at 100%, 125%, and 150% of shoulder width) and in 4 treatment states (offmeds/offstim, offmeds/onstim, onmeds/offstim, onmeds/onstim). With no doorway, the Parkinson's group showed...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5316891</comments>
            <pubDate>Thu, 13 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5316891</guid>        </item>
        <item>
            <title>Pharmacologic approaches to the treatment of Huntington's disease</title>
            <link>http://www.medworm.com/index.php?rid=5316890&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23953</link>
            <description>This article reviews some of the more common pharmacologic treatments used for HD, discusses data regarding suboptimal agents that have been tested, and surveys treatments under investigation. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5316890</comments>
            <pubDate>Thu, 13 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5316890</guid>        </item>
        <item>
            <title>Deep brain stimulation in the treatment of chorea</title>
            <link>http://www.medworm.com/index.php?rid=5316889&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23967</link>
            <description>AbstractDeep brain stimulation has been used as a means of reducing dyskinesias in various conditions, including Parkinson's disease and dystonia for many years. Recently, owing to the clinical similarities between L‐dopa induced dyskinesia and chorea, deep brain stimulation has now been implemented as a novel treatment method in both Huntington's disease and neuroacanthocytosis, and a paucity of case studies exist reporting its efficacy. This review will summarize the case studies of deep brain stimulation in both Huntington's disease and neuroacanthocytosis, and discuss the possible implications and limitations associated with these reports. As both these disorders are often refractory to medication and difficult to treat, deep brain stimulation may be a useful treatment option in the ...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5316889</comments>
            <pubDate>Thu, 13 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5316889</guid>        </item>
        <item>
            <title>Pisa syndrome in Parkinson's disease: Clinical, electromyographic, and radiological characterization</title>
            <link>http://www.medworm.com/index.php?rid=5316888&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23930</link>
            <description>In this study we describe clinical, electromyographic (EMG), and radiological features of PS in a group of 20 PD patients. All patients with trunk deviation underwent EMG and radiological (RX and CT scan) investigation. Clinical characteristics of patients with PS were compared with a control group of PD patients without trunk deviation. PD patients with PS showed a significantly higher score of disease asymmetry compared with the control group. In the majority of patients with PS, trunk bending was contralateral to the side of symptom onset. EMG showed abnormal tonic hyperactivity on the side of the deviation in the paravertebral thoracic muscles and in the abdominal oblique muscles. CT of the lumbar paraspinal muscles showed muscular atrophy more marked on the side of the deviation, with...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5316888</comments>
            <pubDate>Thu, 13 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5316888</guid>        </item>
        <item>
            <title>Cortically evoked responses of human pallidal neurons</title>
            <link>http://www.medworm.com/index.php?rid=5316895&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23886</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5316895</comments>
            <pubDate>Wed, 12 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5316895</guid>        </item>
        <item>
            <title>Handedness correlates with the dominant parkinson side: A systematic review and meta‐analysis</title>
            <link>http://www.medworm.com/index.php?rid=5316894&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24007</link>
            <description>The objective of this study was to establish whether a relation between handedness and dominant PD side exists. We searched for cross‐sectional or cohort studies that registered handedness and onset side in PD patients in PubMed, EMBASE, and Web of Science from their first record until 14 February 2011. Data about handedness and dominant PD side was extracted. Authors who registered both but not described their relation were contacted for further information. Odds ratios (ORs) were analyzed with a fixed effect Mantel‐Haenszel model. Heterogeneity and indications of publication bias were limited. Our electronic search identified 10 studies involving 4405 asymmetric PD patients. Of the right‐handed patients, 2413 (59.5%) had right‐dominant and 1644 (40.5%) had left‐dominant PD symp...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5316894</comments>
            <pubDate>Wed, 12 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5316894</guid>        </item>
        <item>
            <title>Role of serotonergic 1A receptor dysfunction in depression associated with Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5316893&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23895</link>
            <description>The objective of the present study was to use positron emission tomography and [18F]MPPF to investigate the role of postsynaptic serotonergic system dysfunction in the pathophysiology of depression in Parkinson's disease. Four parkinsonian patients with depression and 8 parkinsonian patients without depression were enrolled. Each patient underwent a scan using [18F]MPPF, a selective serotonin 1A receptor antagonist. Voxel‐by‐voxel statistical comparison of [18F]MPPF uptake of the 2 groups of parkinsonian patients and with 7 matched normal subjects was made using statistical parametric mapping (P uncorrected &amp;lt; .001). Compared with nondepressed parkinsonian patients, depressed patients exhibited reduced tracer uptake in the left hippocampus, the right insula, the left superior tempora...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5316893</comments>
            <pubDate>Wed, 12 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5316893</guid>        </item>
        <item>
            <title>Monitoring late complications of zinc treatment in Wilson's disease. Reply to the letter: Copper deficiency in Wilson's disease: An avoidable complication of treatment</title>
            <link>http://www.medworm.com/index.php?rid=5316892&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23969</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5316892</comments>
            <pubDate>Wed, 12 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5316892</guid>        </item>
        <item>
            <title>Reversible parkinsonism due to involvement of substantia nigra in Epstein‐Barr virus encephalitis</title>
            <link>http://www.medworm.com/index.php?rid=5305955&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23935</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5305955</comments>
            <pubDate>Tue, 11 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5305955</guid>        </item>
        <item>
            <title>Risks of inappropriate secretion of antidiuretic hormone in multiple system atrophy</title>
            <link>http://www.medworm.com/index.php?rid=5305956&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23904</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5305956</comments>
            <pubDate>Mon, 10 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5305956</guid>        </item>
        <item>
            <title>Executive functions in Parkinson's disease: Systematic review and meta‐analysis</title>
            <link>http://www.medworm.com/index.php?rid=5287495&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23868</link>
            <description>AbstractImpairment of executive function (EF) is commonly reported as a feature of PD. However, the exact pattern of executive impairment remains unclear. Also, there is an ongoing discussion surrounding the definition and conceptualization of EF, which might affect the clarity of research evidence on cognition in PD. The aim of this systematic review was to describe the pattern of executive impairment in early‐stage PD emerging from the research literature and to identify critical issues for improving consistency in this field. The PsychInfo, MEDLINE, Science Direct, CINAHL, and Cochrane Library databases were searched using the term “Parkinson's disease” combined with each of 14 cognitive abilities defined as representing aspects of EF. The review was limited to studies that invest...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5287495</comments>
            <pubDate>Mon, 03 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5287495</guid>        </item>
        <item>
            <title>Genetic and pathological links between Parkinson's disease and the lysosomal disorder Sanfilippo syndrome</title>
            <link>http://www.medworm.com/index.php?rid=5423727&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24029</link>
            <description>Conclusions:This study suggests a possible role of NAGLU in susceptibility to PD while extending evidence for α‐synuclein aggregation in the brain in lysosomal storage disorders. Our findings support a mechanism involving lysosomal dysfunction more generally in the pathogenesis of PD. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5423727</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5423727</guid>        </item>
        <item>
            <title>Environmental tobacco smoke and Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5410465&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24012</link>
            <description>Conclusions:These observations parallel those well established for active smoking. However, it remains unresolved whether a true protective effect of tobacco smoke, generally detrimental to health, underlies these associations. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410465</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5410465</guid>        </item>
        <item>
            <title>Neuropathology of sporadic Parkinson's disease: Evaluation and changes of concepts</title>
            <link>http://www.medworm.com/index.php?rid=5401668&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23795</link>
            <description>AbstractParkinson's disease (PD), one of the most frequent neurodegenerative disorders, is no longer considered a complex motor disorder characterized by extrapyramidal symptoms, but a progressive multisystem or—more correctly—multiorgan disease with variegated neurological and nonmotor deficiencies. It is morphologically featured not only by the degeneration of the dopaminergic nigrostriatal system, responsible for the core motor deficits, but by multifocal involvement of the central, peripheral and autonomic nervous system and other organs associated with widespread occurrence of Lewy bodies and dystrophic Lewy neurites. This results from deposition of abnormal α‐synuclein (αSyn), the major protein marker of PD, and other synucleinopathies. Recent research has improved both the c...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5401668</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5401668</guid>        </item>
        <item>
            <title>Iowa gambling task in de novo Parkinson's disease: A comparison between good and poor performers</title>
            <link>http://www.medworm.com/index.php?rid=5365446&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23982</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5365446</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5365446</guid>        </item>
        <item>
            <title>Syndromes of neurodegeneration with brain iron accumulation (NBIA): An update on clinical presentations, histological and genetic underpinnings, and treatment considerations</title>
            <link>http://www.medworm.com/index.php?rid=5349721&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23971</link>
            <description>AbstractIn recent years, understanding of the syndromes of neurodegeneration with brain iron accumulation (NBIA) has grown considerably. In addition to the core syndromes of pantothenate kinsase–associated neurodegeneration (PKAN, NBIA1) and PLA2G6‐associated neurodegeneration (PLAN, NBIA2), several other genetic causes have been identified. The acknowledged clinical spectrum has broadened, age‐dependent presentations have been recognized, and we are becoming aware of overlap between the different NBIA disorders as well as with other diseases. Autopsy examination of genetically confirmed cases has demonstrated Lewy bodies and/or tangles in some subforms, bridging the gap to more common neurodegenerative disorders such as Parkinson's disease. NBIA genes map into related pathways, the ...</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5349721</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5349721</guid>        </item>
        <item>
            <title>Projected numbers of people with movement disorders in the years 2030 and 2050</title>
            <link>http://www.medworm.com/index.php?rid=5338157&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23878</link>
            <description>Conclusions:There will be a strong increase in the number of people affected by most movement disorders between 2010 and 2050. This increase will mostly depend on the future aging of populations in terms of their age structure and future life expectancy. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5338157</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5338157</guid>        </item>
        <item>
            <title>Levodopa‐responsive parkinsonism in probable extrapontine myelinolysis of the mesencephalon</title>
            <link>http://www.medworm.com/index.php?rid=5338156&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23876</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5338156</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5338156</guid>        </item>
        <item>
            <title>New Sections for Movement Disorders</title>
            <link>http://www.medworm.com/index.php?rid=5338155&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.24008</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5338155</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5338155</guid>        </item>
        <item>
            <title>Learning PD from the lark</title>
            <link>http://www.medworm.com/index.php?rid=5338154&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23979</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5338154</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5338154</guid>        </item>
        <item>
            <title>Links between glucocerebrosidase and alpha‐synuclein revealed</title>
            <link>http://www.medworm.com/index.php?rid=5338153&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23985</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5338153</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5338153</guid>        </item>
        <item>
            <title>A new twist on turning movements in Parkinson's disease patients</title>
            <link>http://www.medworm.com/index.php?rid=5338152&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23980</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5338152</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5338152</guid>        </item>
        <item>
            <title>Continuing efforts to obtain continuous delivery of levodopa</title>
            <link>http://www.medworm.com/index.php?rid=5338151&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23996</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5338151</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5338151</guid>        </item>
        <item>
            <title>Cerebrospinal fluid fatty acids in glucocerebrosidase‐associated Parkinson's disease</title>
            <link>http://www.medworm.com/index.php?rid=5338149&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23984</link>
            <description>Conclusions:These results suggest that abnormalities of fatty acid metabolism are specifically involved in the pathogenesis of Parkinson's disease associated with a heterozygous glucocerebrosidase mutation. © 2011 Movement Disorder Society (Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5338149</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5338149</guid>        </item>
        <item>
            <title>Changing to interleaving stimulation might improve dystonia in cases not responding to pallidal stimulation</title>
            <link>http://www.medworm.com/index.php?rid=5262613&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23962</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5262613</comments>
            <pubDate>Wed, 28 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5262613</guid>        </item>
        <item>
            <title>Paroxysmal limb dyskinesia induced by weight: An unusual case of cortical reflex seizures</title>
            <link>http://www.medworm.com/index.php?rid=5262612&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23874</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5262612</comments>
            <pubDate>Wed, 28 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5262612</guid>        </item>
        <item>
            <title>Dystonia in mitochondrial spinocerebellar ataxia and epilepsy syndrome associated with novel recessive POLG mutations</title>
            <link>http://www.medworm.com/index.php?rid=5262611&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23960</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5262611</comments>
            <pubDate>Wed, 28 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5262611</guid>        </item>
        <item>
            <title>Reply to: Treatment of tics in patients with Tourette syndrome: Recommendations according to the European Society for the Study of Tourette Syndrome</title>
            <link>http://www.medworm.com/index.php?rid=5262610&amp;cid=s_33605_25_f&amp;fid=33605&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fmds.23957</link>
            <description>(Source: Movement Disorders)</description>
            <author>Movement Disorders</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5262610</comments>
            <pubDate>Wed, 28 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5262610</guid>        </item>
    </channel>
</rss>

