Pantothenate kinase–associated neurodegeneration: Clinical description of 10 patients and identification of new mutations
Identifieur interne : 002320 ( Istex/Corpus ); précédent : 002319; suivant : 002321Pantothenate kinase–associated neurodegeneration: Clinical description of 10 patients and identification of new mutations
Auteurs : Salima Assami ; Hamid Azzedine ; Sonia Nouioua ; Emeline Mundwiller ; Soulaiman Mahoui ; Samira Makri ; Meriam Djemai ; Djamel Grid ; Alexis Brice ; Tarik Hamadouche ; Giovanni Stevanin ; Meriem TazirSource :
- Movement Disorders [ 0885-3185 ] ; 2011-08-01.
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DOI: 10.1002/mds.23648
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This work received support from the Ministère de la Santé, de la Population et de la Réforme Hospitalière (Algeria), the Ministère de l'Enseignement Supérieur et de la Recherche Scientifique (Algeria), the Agence National de la Recherche (France, to A.D. and G.S.), the Association Française contre les Myopathies (AFM, France; to H.A.) and the Verum Foundation (Germany; to A.B.). Full financial disclosures and author roles may be found in the online version of this article.</note></notesStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Pantothenate kinase–associated neurodegeneration: Clinical description of 10 patients and identification of new mutations</title><author><persName><forename type="first">Salima</forename><surname>Assami</surname><roleName type="degree">MD</roleName></persName><affiliation>Department of Neurology, CHU Mustapha Bacha and Laboratoire de Neurosciences, Université d'Alger, Algérie, Algeria</affiliation></author><author><persName><forename type="first">Hamid</forename><surname>Azzedine</surname><roleName type="degree">PhD</roleName></persName><affiliation>INSERM, U975 (formerly U679), Paris, France</affiliation><affiliation>UPMC Univ. 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number="2350"></count></countGroup><titleGroup><title type="main" xml:lang="en">Pantothenate kinase–associated neurodegeneration: Clinical description of 10 patients and identification of new mutations<link href="#fn1"></link></title><title type="short" xml:lang="en">Letters to the Editor</title></titleGroup><creators><creator xml:id="au1" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Salima</givenNames><familyName>Assami</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au2" creatorRole="author" affiliationRef="#af2 #af3"><personName><givenNames>Hamid</givenNames><familyName>Azzedine</familyName><degrees>PhD</degrees></personName></creator><creator xml:id="au3" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Sonia</givenNames><familyName>Nouioua</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au4" creatorRole="author" affiliationRef="#af2 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This work received support from the Ministère de la Santé, de la Population et de la Réforme Hospitalière (Algeria), the Ministère de l'Enseignement Supérieur et de la Recherche Scientifique (Algeria), the Agence National de la Recherche (France, to A.D. and G.S.), the Association Française contre les Myopathies (AFM, France; to H.A.) and the Verum Foundation (Germany; to A.B.). 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This work received support from the Ministère de la Santé, de la Population et de la Réforme Hospitalière (Algeria), the Ministère de l'Enseignement Supérieur et de la Recherche Scientifique (Algeria), the Agence National de la Recherche (France, to A.D. and G.S.), the Association Française contre les Myopathies (AFM, France; to H.A.) and the Verum Foundation (Germany; to A.B.). Full financial disclosures and author roles may be found in the online version of this article.</note><relatedItem type="host"><titleInfo><title>Movement Disorders</title></titleInfo><titleInfo type="abbreviated"><title>Mov. 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