Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α‐synuclein triplication (Iowa kindred)
Identifieur interne : 002311 ( Istex/Corpus ); précédent : 002310; suivant : 002312Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α‐synuclein triplication (Iowa kindred)
Auteurs : Katrina Gwinn ; Michael J. Devine ; Lee-Way Jin ; Janel Johnson ; Thomas Bird ; Manfred Muenter ; Cheryl Waters ; Charles H. Adler ; Richard Caselli ; Henry Houlden ; Grisel Lopez ; Amanda Singleton ; John Hardy ; Andrew SingletonSource :
- Movement Disorders [ 0885-3185 ] ; 2011-09.
Url:
DOI: 10.1002/mds.23776
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ISTEX:61D1E5E23E7B45F1F67440224E405FBF7D101A92Le document en format XML
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Devine contributed equally to this work.</note><affiliation>Katrina Gwinn and Michael J. Devine contributed equally to this work.</affiliation><affiliation>National Institutes of Neurological Disorders and Stroke, Bethesda, Maryland, USA</affiliation></author><author><persName><forename type="first">Michael J.</forename><surname>Devine</surname></persName><note type="biography">Katrina Gwinn and Michael J. Devine contributed equally to this work.</note><affiliation>Katrina Gwinn and Michael J. Devine contributed equally to this work.</affiliation><note type="correspondence"><p>Correspondence: Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London, United Kingdom</p></note><affiliation>Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London, United Kingdom</affiliation></author><author><persName><forename type="first">Lee‐Way</forename><surname>Jin</surname><roleName type="degree">MD, PhD</roleName></persName><affiliation>University of Washington, Seattle, Washington, USA</affiliation></author><author><persName><forename type="first">Janel</forename><surname>Johnson</surname><roleName type="degree">BA</roleName></persName><affiliation>National Institutes of Neurological Disorders and Stroke, Bethesda, Maryland, USA</affiliation></author><author><persName><forename type="first">Thomas</forename><surname>Bird</surname><roleName type="degree">MD</roleName></persName><affiliation>University of Washington, Seattle, Washington, USA</affiliation></author><author><persName><forename type="first">Manfred</forename><surname>Muenter</surname><roleName type="degree">MD</roleName></persName><affiliation>Mayo Clinic, Scottsdale, Arizona, USA</affiliation></author><author><persName><forename type="first">Cheryl</forename><surname>Waters</surname><roleName type="degree">MD</roleName></persName><affiliation>Columbia University College of Physicians and Surgeons, New York, New York, USA</affiliation></author><author><persName><forename type="first">Charles H.</forename><surname>Adler</surname><roleName type="degree">MD, PhD</roleName></persName><affiliation>Mayo Clinic, Scottsdale, Arizona, USA</affiliation></author><author><persName><forename type="first">Richard</forename><surname>Caselli</surname><roleName type="degree">MD</roleName></persName><affiliation>Mayo Clinic, Scottsdale, Arizona, USA</affiliation></author><author><persName><forename type="first">Henry</forename><surname>Houlden</surname><roleName type="degree">MD, PhD</roleName></persName><affiliation>Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London, United Kingdom</affiliation></author><author><persName><forename type="first">Grisel</forename><surname>Lopez</surname><roleName type="degree">MD</roleName></persName><affiliation>National Human Genome Research Institute, Bethesda, Maryland, USA</affiliation></author><author><persName><forename type="first">Amanda</forename><surname>Singleton</surname><roleName type="degree">BS</roleName></persName><affiliation>National Institutes of Neurological Disorders and Stroke, Bethesda, Maryland, USA</affiliation></author><author><persName><forename type="first">John</forename><surname>Hardy</surname><roleName type="degree">PhD</roleName></persName><affiliation>Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London, United Kingdom</affiliation></author><author><persName><forename type="first">Andrew</forename><surname>Singleton</surname><roleName type="degree">PhD</roleName></persName><affiliation>National Institute for Aging, Bethesda Marylandd, USA</affiliation></author></analytic><monogr><title level="j">Movement Disorders</title><title level="j" type="abbrev">Mov. 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Information</caption></supportingInfoItem></supportingInformation></contentMeta><noteGroup><note xml:id="fn2"><p>Relevant conflicts of interest/financial disclosures: Nothing to report.</p></note><note xml:id="fn3"><p>Full financial disclosures and author roles may be found in the online version of this article.</p></note><note xml:id="fn1"><p>Katrina Gwinn and Michael J. Devine contributed equally to this work.</p></note></noteGroup></header></component></istex:document></istex:metadataXml><!--Version 0.6 générée le 3-12-2015--><mods version="3.6"><titleInfo lang="en"><title>Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α‐synuclein triplication (Iowa kindred)</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Letters to the Editors</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α‐synuclein triplication (Iowa kindred)</title></titleInfo><name type="personal"><namePart type="given">Katrina</namePart><namePart type="family">Gwinn</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>National Institutes of Neurological Disorders and Stroke, Bethesda, Maryland, USA</affiliation><description>Katrina Gwinn and Michael J. 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