Your browser doesn't support javascript.
loading
Oculogyric crises in PLA2G6 associated neurodegeneration.
Rohani, Mohammad; Shahidi, Gholamali; Vali, Farzaneh; Lang, Anthony E; Slow, Elizabeth; Gahl, William A; Behnam, Babak.
Afiliación
  • 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 en En | MEDLINE | ID: mdl-29574084
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Distrofias Neuroaxonales / Trastornos del Metabolismo del Hierro / Trastornos Heredodegenerativos del Sistema Nervioso / Distonía / Fosfolipasas A2 Grupo VI Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Adult / Humans / Male Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Irán
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Distrofias Neuroaxonales / Trastornos del Metabolismo del Hierro / Trastornos Heredodegenerativos del Sistema Nervioso / Distonía / Fosfolipasas A2 Grupo VI Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Adult / Humans / Male Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Irán