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SPG11 presenting with dystonic tremor in childhood.
Innes, Emily A; Goetti, Robert; Mahant, Neil; Ho, Gladys; Williams, Laura; Gill, Deepak; Dale, Russell C; Mohammad, Shekeeb S.
Afiliación
  • Innes EA; TY Nelson Department of Neurology and Neurosurgery, The Children's Hospital at Westmead, NSW, Sydney, Australia; School of Medicine Sydney, The University of Notre Dame, Sydney, Australia. Electronic address: shekeeb.mohammad@health.nsw.gov.au.
  • Goetti R; Medical Imaging, The Children's Hospital at Westmead, Australia; Sydney Genome Diagnostics, Western Sydney Genetics Program, The Children's Hospital at Westmead, NSW, Sydney, Australia.
  • Mahant N; Movement Disorders Unit, Neurology Department, Westmead Hospital, Westmead, New South Wales, Australia.
  • Ho G; Sydney Genome Diagnostics, Western Sydney Genetics Program, The Children's Hospital at Westmead, NSW, Sydney, Australia; Sydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
  • Williams L; Movement Disorders Unit, Neurology Department, Westmead Hospital, Westmead, New South Wales, Australia.
  • Gill D; TY Nelson Department of Neurology and Neurosurgery, The Children's Hospital at Westmead, NSW, Sydney, Australia; Kids Neuroscience Centre, The Children's Hospital at Westmead, NSW, Sydney, Australia.
  • Dale RC; Kids Neuroscience Centre, The Children's Hospital at Westmead, NSW, Sydney, Australia; Sydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
  • Mohammad SS; TY Nelson Department of Neurology and Neurosurgery, The Children's Hospital at Westmead, NSW, Sydney, Australia; Kids Neuroscience Centre, The Children's Hospital at Westmead, NSW, Sydney, Australia; Sydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
Parkinsonism Relat Disord ; 99: 76-78, 2022 06.
Article en En | MEDLINE | ID: mdl-35617747
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Humans Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Humans Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article