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PSP-Richardson's Syndrome as a Rare Phenotypic Expression of Very Late-Onset Huntington's Disease: A Case Report.
Prange, Stephane; Laurencin, Chloé; Roche, Pauline; Quadrio, Isabelle; Thobois, Stéphane.
Afiliação
  • Prange S; Hospices Civils de Lyon, Department of Neurology C, Expert Parkinson Center NS-PARK/FCRIN, Pierre Wertheimer Neurological Hospital, Bron, France.
  • Laurencin C; Univ Lyon, Marc Jeannerod Cognitive Neuroscience Institute, CNRS, UMR 5229, Bron, France.
  • Roche P; Univ Lyon, Faculté de Médecine et de Maïeutique Lyon Sud Charles Mérieux, Université Claude Bernard Lyon 1, Oullins, France.
  • Quadrio I; Hospices Civils de Lyon, Department of Neurology C, Expert Parkinson Center NS-PARK/FCRIN, Pierre Wertheimer Neurological Hospital, Bron, France.
  • Thobois S; Hospices Civils de Lyon, Department of Neurology C, Expert Parkinson Center NS-PARK/FCRIN, Pierre Wertheimer Neurological Hospital, Bron, France.
Mov Disord Clin Pract ; 11(3): 303-305, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38173343
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paralisia Supranuclear Progressiva / Doença de Huntington Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paralisia Supranuclear Progressiva / Doença de Huntington Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article