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Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy.
Matej, Radoslav; Kovacs, Gabor G; Johanidesová, Silvie; Keller, Jirí; Matejcková, Milada; Nováková, Jana; Sigut, Vladimír; Keller, Otakar; Rusina, Robert.
Affiliation
  • Matej R; Department of Pathology and Molecular Medicine, Thomayer Teaching Hospital, Prague, Czech Republic.
Mov Disord ; 27(4): 476-9, 2012 Apr.
Article in En | MEDLINE | ID: mdl-22488860
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arginine / Supranuclear Palsy, Progressive / Prions / Creutzfeldt-Jakob Syndrome / Mutation Limits: Female / Humans / Middle aged Language: En Journal: Mov Disord Journal subject: NEUROLOGIA Year: 2012 Document type: Article Affiliation country: Czech Republic
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arginine / Supranuclear Palsy, Progressive / Prions / Creutzfeldt-Jakob Syndrome / Mutation Limits: Female / Humans / Middle aged Language: En Journal: Mov Disord Journal subject: NEUROLOGIA Year: 2012 Document type: Article Affiliation country: Czech Republic