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Oculogyric crises in PLA2G6 associated neurodegeneration.
Rohani, Mohammad; Shahidi, Gholamali; Vali, Farzaneh; Lang, Anthony E; Slow, Elizabeth; Gahl, William A; Behnam, Babak.
Afiliação
  • Rohani M; Department of Neurology, Hazrat Rasool Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Shahidi G; Department of Neurology, Hazrat Rasool Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Vali F; Department of Medical Genetics and Molecular Biology, Iran University of Medical Sciences, Tehran, Iran.
  • Lang AE; Morton and Gloria Shulman Movement Disorders Clinic and the Edmond J. Safra Program in Parkinson's Disease, Toronto Western Hospital and Division of Neurology, University of Toronto, Toronto, Ontario, Canada; Krembil Research Institute, Toronto, Ontario, Canada.
  • Slow E; Morton and Gloria Shulman Movement Disorders Clinic and the Edmond J. Safra Program in Parkinson's Disease, Toronto Western Hospital and Division of Neurology, University of Toronto, Toronto, Ontario, Canada; Krembil Research Institute, Toronto, Ontario, Canada.
  • Gahl WA; Medical Genetics Branch, National Human Genome Research Institute (NHGRI), Undiagnosed Diseases Program, Common Fund, Office of the Director, National Institutes of Health, Bethesda, MD, USA.
  • Behnam B; Department of Medical Genetics and Molecular Biology, Iran University of Medical Sciences, Tehran, Iran; Medical Genetics Branch, National Human Genome Research Institute (NHGRI), Undiagnosed Diseases Program, Common Fund, Office of the Director, National Institutes of Health, Bethesda, MD, USA. Ele
Parkinsonism Relat Disord ; 52: 111-112, 2018 07.
Article em En | MEDLINE | ID: mdl-29574084
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distrofias Neuroaxonais / Distúrbios do Metabolismo do Ferro / Transtornos Heredodegenerativos do Sistema Nervoso / Distonia / Fosfolipases A2 do Grupo VI Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Adult / Humans / Male Idioma: En Revista: Parkinsonism Relat Disord Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distrofias Neuroaxonais / Distúrbios do Metabolismo do Ferro / Transtornos Heredodegenerativos do Sistema Nervoso / Distonia / Fosfolipases A2 do Grupo VI Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Adult / Humans / Male Idioma: En Revista: Parkinsonism Relat Disord Ano de publicação: 2018 Tipo de documento: Article