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Infantile-Onset Paroxysmal Movement Disorder and Episodic Ataxia Associated with a TBC1D24 Mutation.
Zimmern, Vincent; Riant, Florence; Roze, Emmanuel; Ranza, Emmanuelle; Lehmann-Horn, Frank; de Bellescize, Julitta; Ville, Dorothée; Lesca, Gaetan; Korff, Christian M.
Afiliação
  • Zimmern V; Division of Pediatric Neurology, University of Texas Southwestern, Dallas, Texas, United States.
  • Riant F; Laboratoire de Génétique Moléculaire Neurovasculaire, Groupe Hospitalier Saint-Louis-Lariboisière-Fernand-Widal, Paris, France.
  • Roze E; Sorbonne Université, Faculté de Médecine ; CNRS UMR 7225, UMR S 1127 ; Institut du Cerveau et de la Moelle épinière; APHP, Hôpital Salpêtrière, Département de Neurologie, Paris, France.
  • Ranza E; Service of Genetic Medicine, University Hospitals, Geneva, Switzerland.
  • Lehmann-Horn F; Department of Neurophysiology, Ulm University, Ulm, Germany.
  • de Bellescize J; Department of Paediatric Clinical Epileptology, Sleep Disorders and Functional Neurology, Hospices Civils de Lyon, Lyon, France.
  • Ville D; Centre de référence « Déficiences Intellectuelles de causes rares ¼, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, Bron, France.
  • Lesca G; Centre de référence des anomalies du développement, Service de Génétique, Hospices Civils de Lyon, Bron, France.
  • Korff CM; Pediatric Neurology, Child and Adolescent Department, University Hospitals, Geneva, Switzerland.
Neuropediatrics ; 50(5): 308-312, 2019 10.
Article em En | MEDLINE | ID: mdl-31226716
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia / Proteínas Ativadoras de GTPase / Transtornos dos Movimentos Tipo de estudo: Risk_factors_studies Limite: Humans / Infant / Male Idioma: En Revista: Neuropediatrics Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia / Proteínas Ativadoras de GTPase / Transtornos dos Movimentos Tipo de estudo: Risk_factors_studies Limite: Humans / Infant / Male Idioma: En Revista: Neuropediatrics Ano de publicação: 2019 Tipo de documento: Article