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Fast versus slow disease progression in amyotrophic lateral sclerosis-clinical and genetic factors at the edges of the survival spectrum.
Witzel, Simon; Wagner, Matias; Zhao, Chen; Kandler, Katharina; Graf, Elisabeth; Berutti, Riccardo; Oexle, Konrad; Brenner, David; Winkelmann, Juliane; Ludolph, Albert C.
Afiliación
  • Witzel S; Ulm University, Department of Neurology, Ulm, Germany; German Center for Neurodegenerative Diseases (DZNE), Site Ulm, Ulm, Germany. Electronic address: simon.witzel@uni-ulm.de.
  • Wagner M; Technical University of Munich, Institute of Human Genetics, School of Medicine, Munich, Germany; Institute of Neurogenomics, Helmholtz Zentrum München GmbH, German Research Center for Environmental Health, Neuherberg, Germany.
  • Zhao C; Institute of Neurogenomics, Helmholtz Zentrum München GmbH, German Research Center for Environmental Health, Neuherberg, Germany.
  • Kandler K; Ulm University, Department of Neurology, Ulm, Germany.
  • Graf E; Institute of Neurogenomics, Helmholtz Zentrum München GmbH, German Research Center for Environmental Health, Neuherberg, Germany.
  • Berutti R; Technical University of Munich, Institute of Human Genetics, School of Medicine, Munich, Germany.
  • Oexle K; Institute of Neurogenomics, Helmholtz Zentrum München GmbH, German Research Center for Environmental Health, Neuherberg, Germany.
  • Brenner D; Ulm University, Department of Neurology, Ulm, Germany.
  • Winkelmann J; Institute of Neurogenomics, Helmholtz Zentrum München GmbH, German Research Center for Environmental Health, Neuherberg, Germany; Munich Cluster for Systems Neurology, Munich, Germany; Department of Neurogenetics Technical University of Munich, Munich, Germany.
  • Ludolph AC; Ulm University, Department of Neurology, Ulm, Germany; German Center for Neurodegenerative Diseases (DZNE), Site Ulm, Ulm, Germany.
Neurobiol Aging ; 119: 117-126, 2022 11.
Article en En | MEDLINE | ID: mdl-35933239
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Esclerosis Amiotrófica Lateral Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Neurobiol Aging Año: 2022 Tipo del documento: Article
Texto completo
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Esclerosis Amiotrófica Lateral Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Neurobiol Aging Año: 2022 Tipo del documento: Article