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Morbus Fabry and Parkinson's Disease-More Evidence for a Possible Genetic Link.
Müller, Susanne; Kassubek, Jan; Hold, Stephan T; Kasper, David C; Mayer, Benjamin; Müller, Kathrin; Freischmidt, Axel; Siebert, Reiner; Braak, Heiko; Ludolph, Albert C; Del Tredici, Kelly.
Afiliação
  • Müller S; Department of Neurology, University of Ulm, Ulm, Germany.
  • Kassubek J; Department of Neurology, University of Ulm, Ulm, Germany.
  • Hold ST; German Center for Neurodegenerative Diseases (DZNE), Ulm, Germany.
  • Kasper DC; ARCHIMED Life Science GmbH, Vienna, Austria.
  • Mayer B; ARCHIMED Life Science GmbH, Vienna, Austria.
  • Müller K; Institute of Epidemiology and Medical Biometry, University of Ulm, Ulm, Germany.
  • Freischmidt A; Department of Neurology, University of Ulm, Ulm, Germany.
  • Siebert R; Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany.
  • Braak H; Department of Neurology, University of Ulm, Ulm, Germany.
  • Ludolph AC; Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany.
  • Del Tredici K; Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany.
Mov Disord ; 39(2): 449-451, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38226450
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Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Doença de Fabry Limite: Humans Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Alemanha
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Doença de Fabry Limite: Humans Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Alemanha