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Clinicopathological Relationships in an Aged Case of DOORS Syndrome With a p.Arg506X Mutation in the ATP6V1B2 Gene.
Zádori, Dénes; Szalárdy, Levente; Reisz, Zita; Kovacs, Gabor G; Maszlag-Török, Rita; Ajeawung, Norbert F; Vécsei, László; Campeau, Philippe M; Klivényi, Péter.
Afiliação
  • Zádori D; Department of Neurology, Interdisciplinary Excellence Center, Faculty of Medicine, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, Hungary.
  • Szalárdy L; Department of Neurology, Interdisciplinary Excellence Center, Faculty of Medicine, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, Hungary.
  • Reisz Z; Department of Pathology, Faculty of Medicine, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, Hungary.
  • Kovacs GG; Institute of Neurology, Medical University of Vienna, Vienna, Austria.
  • Maszlag-Török R; Department of Laboratory Medicine and Pathobiology, Tanz Centre for Research in Neurodegenerative Disease, University of Toronto, Toronto, ON, Canada.
  • Ajeawung NF; Laboratory Medicine Program & Krembil Brain Institute, University Health Network, Toronto, ON, Canada.
  • Vécsei L; Department of Neurology, Interdisciplinary Excellence Center, Faculty of Medicine, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, Hungary.
  • Campeau PM; CHU Sainte-Justine Research Center, Université de Montréal, Montreal, QC, Canada.
  • Klivényi P; Department of Neurology, Interdisciplinary Excellence Center, Faculty of Medicine, Albert Szent-Györgyi Clinical Center, University of Szeged, Szeged, Hungary.
Front Neurol ; 11: 767, 2020.
Article em En | MEDLINE | ID: mdl-32849222

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Neurol Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Neurol Ano de publicação: 2020 Tipo de documento: Article