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Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations.
Brenner, David; Rosenbohm, Angela; Yilmaz, Rüstem; Müller, Kathrin; Grehl, Torsten; Petri, Susanne; Meyer, Thomas; Grosskreutz, Julian; Weydt, Patrick; Ruf, Wolfgang; Neuwirth, Christoph; Weber, Markus; Pinto, Susana; Claeys, Kristl G; Schrank, Berthold; Jordan, Berit; Knehr, Antje; Günther, Kornelia; Hübers, Annemarie; Zeller, Daniel; Kubisch, Christian; Jablonka, Sibylle; Sendtner, Michael; Klopstock, Thomas; de Carvalho, Mamede; Sperfeld, Anne; Borck, Guntram; Volk, Alexander E; Dorst, Johannes; Weis, Joachim; Otto, Markus; Schuster, Joachim; Del Tredici, Kelly; Braak, Heiko; Danzer, Karin M; Freischmidt, Axel; Meitinger, Thomas; Ludolph, Albert C; Andersen, Peter M; Weishaupt, Jochen H.
Afiliación
  • Brenner D; Neurology Department, Ulm University, Ulm, Germany.
  • Rosenbohm A; Neurology Department, Ulm University, Ulm, Germany.
  • Yilmaz R; Neurology Department, Ulm University, Ulm, Germany.
  • Müller K; Neurology Department, Ulm University, Ulm, Germany.
  • Grehl T; Department of Neurology, Alfried Krupp Hospital, Essen, Germany.
  • Petri S; Department of Neurology, Hannover Medical School, Hannover, Germany.
  • Meyer T; Charité University Hospital, Humboldt-University, Berlin, Germany.
  • Grosskreutz J; Department of Neurology, Jena University Hospital, Jena, Germany.
  • Weydt P; Neurology Department, Ulm University, Ulm, Germany.
  • Ruf W; Department for Neurodegenerative Disorders and Gerontopsychiatry, Bonn University, Bonn, Germany.
  • Neuwirth C; Neurology Department, Ulm University, Ulm, Germany.
  • Weber M; Kantonsspital St. Gallen, ALS Outpatient Clinic, St. Gallen, Switzerland.
  • Pinto S; Kantonsspital St. Gallen, ALS Outpatient Clinic, St. Gallen, Switzerland.
  • Claeys KG; Department of Neurosciences and Mental Health, Hospital de Santa Maria-CHLN, Lisbon, Portugal.
  • Schrank B; Department of Pharmacology and Clinical Neuroscience, Umeå University, Umeå, Sweden.
  • Jordan B; Institute of Neuropathology, RWTH Aachen University Hospital, Aachen, Germany.
  • Knehr A; Department of Neurology, RWTH Aachen University Hospital, Aachen, Germany.
  • Günther K; Department of Neurology, University Hospitals Leuven, Leuven, Belgium.
  • Hübers A; Laboratory for Muscle Diseases and Neuropathies, Department of Neurosciences, Experimental Neurology, KU Leuven, University of Leuven, Leuven, Belgium.
  • Zeller D; Department of Neurology, DKD HELIOS Klinik Wiesbaden, Wiesbaden, Germany.
  • Kubisch C; Department of Neurology Martin-Luther-University Halle-Wittenberg, Halle/Saale, Germany.
  • Jablonka S; Neurology Department, Ulm University, Ulm, Germany.
  • Sendtner M; Neurology Department, Ulm University, Ulm, Germany.
  • Klopstock T; Neurology Department, Ulm University, Ulm, Germany.
  • de Carvalho M; Department of Neurology, University of Würzburg, Würzburg, Germany.
  • Sperfeld A; Institute of Human Genetics, Ulm University, Ulm, Germany.
  • Borck G; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Volk AE; Institute of Clinical Neurobiology, University Hospital of Würzburg, Würzburg, Germany.
  • Dorst J; Institute of Clinical Neurobiology, University Hospital of Würzburg, Würzburg, Germany.
  • Weis J; Department of Neurology with Friedrich-Baur-Institute, University of Munich, Munich, Germany.
  • Otto M; German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
  • Schuster J; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.
  • Del Tredici K; Department of Neurosciences and Mental Health, Hospital de Santa Maria-CHLN, Lisbon, Portugal.
  • Braak H; Instituto de Medicina Molecular and Institute of Physiology, Faculty of Medicine, University of Lisbon, Portugal.
  • Danzer KM; Department of Neurology Martin-Luther-University Halle-Wittenberg, Halle/Saale, Germany.
  • Freischmidt A; Institute of Human Genetics, Ulm University, Ulm, Germany.
  • Meitinger T; Institute of Human Genetics, Ulm University, Ulm, Germany.
  • Ludolph AC; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Andersen PM; Neurology Department, Ulm University, Ulm, Germany.
  • Weishaupt JH; Institute of Neuropathology, RWTH Aachen University Hospital, Aachen, Germany.
Brain ; 142(12): e67, 2019 12 01.
Article en En | MEDLINE | ID: mdl-31612906
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Atrofia Muscular Espinal Tipo de estudio: Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: Brain Año: 2019 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Atrofia Muscular Espinal Tipo de estudio: Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: Brain Año: 2019 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido