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Clinicopathological description of two cases with SQSTM1 gene mutation associated with frontotemporal dementia.
Kovacs, Gabor G; van der Zee, Julie; Hort, Jakub; Kristoferitsch, Wolfgang; Leitha, Thomas; Höftberger, Romana; Ströbel, Thomas; Van Broeckhoven, Christine; Matej, Radoslav.
Afiliação
  • Kovacs GG; Institute of Neurology, Medical University of Vienna, Vienna, Austria.
  • van der Zee J; Neurodegenerative Brain Diseases group, Department of Molecular Genetics, Antwerp, VIB, Belgium.
  • Hort J; Laboratory of Neurogenetics, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium.
  • Kristoferitsch W; Memory Disorders Clinic, Department of Neurology, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, Czech Republic.
  • Leitha T; International Clinical Research Center, St. Anne's University Hospital Brno, Brno, Czech Republic.
  • Höftberger R; Karl Landsteiner Institute for Neuroimmunological and Neurodegenerative Disorders, SMZ-Ost- Donauspital, Vienna, Austria.
  • Ströbel T; Department of Nuclear Medicine, SMZ-Ost-Donauspital, Vienna, Austria.
  • Van Broeckhoven C; Institute of Neurology, Medical University of Vienna, Vienna, Austria.
  • Matej R; Institute of Neurology, Medical University of Vienna, Vienna, Austria.
Neuropathology ; 36(1): 27-38, 2016 Feb.
Article em En | MEDLINE | ID: mdl-26234378
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Adaptadoras de Transdução de Sinal / Demência Frontotemporal Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Adaptadoras de Transdução de Sinal / Demência Frontotemporal Idioma: En Ano de publicação: 2016 Tipo de documento: Article