A new genetic variant, presenting as young onset rapidly progressive dementia and parkinsonism.

Eissazade, Negin; Alavi, Afagh; Lang, Anthony E; Rohani, Mohammad; Emamikhah, Maziar; Khoeini, Tara

Eissazade, Negin; Alavi, Afagh; Lang, Anthony E; Rohani, Mohammad; Emamikhah, Maziar; Khoeini, Tara.

Afiliación

Eissazade N; School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Alavi A; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Lang AE; Edmond J Safra Program in Parkinson's Disease and the Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital, UHN, Division of Neurology, University of Toronto, Toronto, Ontario, Canada.
Rohani M; Department of Neurology, School of Medicine, Rasool Akram Hospital, Iran University of Medical Sciences, Tehran, Iran; Skull Base Research Center, Five Senses Health Institute, Iran University of Medical Sciences, Tehran, Iran.
Emamikhah M; Department of Neurology, School of Medicine, Rasool Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
Khoeini T; Department of Neurology, School of Medicine, Firoozgar Hospital, Iran University of Medical Sciences, Tehran, Iran. Electronic address: tara.khoeini@gmail.com.

Parkinsonism Relat Disord ; : 105849, 2023 Sep 09.

Article en En | MEDLINE | ID: mdl-37726184

Palabras clave

Alpha-synuclein; Hereditary parkinsonism; Homozygous SNCA mutation; Rapidly progressive dementia

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Irán Pais de publicación: Reino Unido

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google