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ALS and MMN mimics in patients with BSCL2 mutations: the expanding clinical spectrum of SPG17 hereditary spastic paraplegia.
Musacchio, Thomas; Zaum, Ann-Kathrin; Üçeyler, Nurcan; Sommer, Claudia; Pfeifroth, Nora; Reiners, Karlheinz; Kunstmann, Erdmute; Volkmann, Jens; Rost, Simone; Klebe, Stephan.
Afiliación
  • Musacchio T; Department of Neurology, University Hospital Würzburg, Würzburg, Germany.
  • Zaum AK; Department of Human Genetics, University of Würzburg, Würzburg, Germany.
  • Üçeyler N; Department of Neurology, University Hospital Würzburg, Würzburg, Germany.
  • Sommer C; Department of Neurology, University Hospital Würzburg, Würzburg, Germany.
  • Pfeifroth N; Department of Neurology, University Hospital Würzburg, Würzburg, Germany.
  • Reiners K; Department of Neurology, University Hospital Würzburg, Würzburg, Germany.
  • Kunstmann E; Department of Human Genetics, University of Würzburg, Würzburg, Germany.
  • Volkmann J; Department of Neurology, University Hospital Würzburg, Würzburg, Germany.
  • Rost S; Department of Human Genetics, University of Würzburg, Würzburg, Germany.
  • Klebe S; Department of Neurology, University Hospital Würzburg, Würzburg, Germany. stephan.klebe@uniklinik-freiburg.de.
J Neurol ; 264(1): 11-20, 2017 Jan.
Article en En | MEDLINE | ID: mdl-27738760
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria / Subunidades gamma de la Proteína de Unión al GTP / Esclerosis Amiotrófica Lateral / Mutación Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Neurol Año: 2017 Tipo del documento: Article
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria / Subunidades gamma de la Proteína de Unión al GTP / Esclerosis Amiotrófica Lateral / Mutación Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Neurol Año: 2017 Tipo del documento: Article