Evento

PSEN1 mutation (l166v) in an argentine case with familial early onset alzheimer's disease and amyloid angiopathy

Barbieri Kennedy, Micaela; Chrem Mendez, Patricio Alexis; Riudavets, Miguel Angel; Itzcovich, Tatiana; Niikado, MatíasIcon ; Martinetto, Horacio EnriqueIcon ; Allegri, Ricardo FranciscoIcon ; Sevlever, Gustavo; Surace, Ezequiel IgnacioIcon
Tipo del evento: Conferencia
Nombre del evento: Alzheimer's Association International Conference
Fecha del evento: 14/07/2019
Institución Organizadora: Alzheimer's Association;
Título de la revista: Alzheimer's and Dementia
Editorial: Elsevier
ISSN: 1552-5260
Idioma: Inglés
Clasificación temática:

Resumen

Mutations in PSEN1 are the most common cause of familial early‐onset Alzheimer's disease. Here we present an Argentine patient, with a family history of autosomal dominant early‐onset Alzheimer's disease, who developed memory impairment at the age of 40 and died at 50.
Palabras clave: Alzheimer's Disease , Genetics , Brain bank , Variant
 
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info:eu-repo/semantics/restrictedAccess Excepto donde se diga explícitamente, este item se publica bajo la siguiente descripción: Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Unported (CC BY-NC-SA 2.5)
Identificadores
URI: http://hdl.handle.net/11336/129528
URL: https://alz-journals.onlinelibrary.wiley.com/doi/full/10.1016/j.jalz.2019.06.376
DOI: http://dx.doi.org/10.1016/j.jalz.2019.06.3760
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Citación
PSEN1 mutation (l166v) in an argentine case with familial early onset alzheimer's disease and amyloid angiopathy; Alzheimer's Association International Conference; Los Angeles; Estados Unidos; 2019; P1313-P1313
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