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Atypical parkinsonism of progressive supranuclear palsy-parkinsonism (PSP-P) phenotype with rare variants in FBXO7 and VPS35 genes associated with Lewy body pathology.
Mensíková, Katerina; Tucková, Lucie; Kolariková, Kristýna; Bartoníková, Tereza; Vodicka, Radek; Ehrmann, Jiri; Vrtel, Radek; Procházka, Martin; Kanovský, Petr; Kovacs, Gabor G.
Afiliação
  • Mensíková K; Department of Neurology, Faculty of Medicine and Dentistry, Palacky University, University Hospital, I. P. Pavlova 6, 775 20, Olomouc, Czech Republic. katerina.mensikova@fnol.cz.
  • Tucková L; Department of Pathology, Faculty of Medicine and Dentistry, Palacky University, University Hospital, Olomouc, Czech Republic.
  • Kolariková K; Department of Medical Genetics, Faculty of Medicine and Dentistry, Palacky University, University Hospital, Olomouc, Czech Republic.
  • Bartoníková T; Department of Neurology, Faculty of Medicine and Dentistry, Palacky University, University Hospital, I. P. Pavlova 6, 775 20, Olomouc, Czech Republic.
  • Vodicka R; Department of Medical Genetics, Faculty of Medicine and Dentistry, Palacky University, University Hospital, Olomouc, Czech Republic.
  • Ehrmann J; Department of Pathology, Faculty of Medicine and Dentistry, Palacky University, University Hospital, Olomouc, Czech Republic.
  • Vrtel R; Department of Medical Genetics, Faculty of Medicine and Dentistry, Palacky University, University Hospital, Olomouc, Czech Republic.
  • Procházka M; Department of Medical Genetics, Faculty of Medicine and Dentistry, Palacky University, University Hospital, Olomouc, Czech Republic.
  • Kanovský P; Department of Neurology, Faculty of Medicine and Dentistry, Palacky University, University Hospital, I. P. Pavlova 6, 775 20, Olomouc, Czech Republic.
  • Kovacs GG; Klinisches Institut für Neurologie, Medizinische Universität Wien, Vienna, Austria.
Acta Neuropathol ; 137(1): 171-173, 2019 01.
Article em En | MEDLINE | ID: mdl-30374525
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Paralisia Supranuclear Progressiva / Transtornos Parkinsonianos / Proteínas de Transporte Vesicular / Proteínas F-Box Tipo de estudo: Diagnostic_studies / Risk_factors_studies Limite: Aged80 / Humans / Male Idioma: En Revista: Acta Neuropathol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: República Tcheca
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Paralisia Supranuclear Progressiva / Transtornos Parkinsonianos / Proteínas de Transporte Vesicular / Proteínas F-Box Tipo de estudo: Diagnostic_studies / Risk_factors_studies Limite: Aged80 / Humans / Male Idioma: En Revista: Acta Neuropathol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: República Tcheca