Your browser doesn't support javascript.
loading
Co-incidental C9orf72 expansion mutation-related frontotemporal lobar degeneration pathology and sporadic Creutzfeldt-Jakob disease.
Klotz, Sigrid; König, Theresa; Erdler, Marcus; Ulram, Andreas; Nguyen, Anita; Ströbel, Thomas; Zimprich, Alexander; Stögmann, Elisabeth; Regelsberger, Günther; Höftberger, Romana; Budka, Herbert; Kovacs, Gabor G; Gelpi, Ellen.
Afiliação
  • Klotz S; Division of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna, Vienna, Austria.
  • König T; Austrian Reference Center for Human Prion Diseases (OERPE), Vienna, Austria.
  • Erdler M; Department of Neurology, Medical University of Vienna, Vienna, Austria.
  • Ulram A; Department of Neurology, Klinik Donaustadt mit Ludwig-Boltzmann-Institut, Vienna, Austria.
  • Nguyen A; Department of Neurosurgery, Krankenanstalt Rudolfstiftung, Vienna, Austria.
  • Ströbel T; Division of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna, Vienna, Austria.
  • Zimprich A; Division of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna, Vienna, Austria.
  • Stögmann E; Austrian Reference Center for Human Prion Diseases (OERPE), Vienna, Austria.
  • Regelsberger G; Department of Neurology, Medical University of Vienna, Vienna, Austria.
  • Höftberger R; Department of Neurology, Medical University of Vienna, Vienna, Austria.
  • Budka H; Division of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna, Vienna, Austria.
  • Kovacs GG; Austrian Reference Center for Human Prion Diseases (OERPE), Vienna, Austria.
  • Gelpi E; Division of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna, Vienna, Austria.
Eur J Neurol ; 28(3): 1009-1015, 2021 03.
Article em En | MEDLINE | ID: mdl-33131137
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Creutzfeldt-Jakob / Degeneração Lobar Frontotemporal / Demência Frontotemporal / Esclerose Lateral Amiotrófica Tipo de estudo: Prognostic_studies Limite: Aged / Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Creutzfeldt-Jakob / Degeneração Lobar Frontotemporal / Demência Frontotemporal / Esclerose Lateral Amiotrófica Tipo de estudo: Prognostic_studies Limite: Aged / Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article