Cargando…
Gelsolin variant amyloidosis mimicking progressive bulbar palsy
Autores principales: | Park, Jinseok, Kim, Young‐Eun, Oh, Ki‐Wook, Nahm, Minyeop, Kim, Yu Jeong, Kim, Mi Jung, Kim, Seung Hyun |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826199/ https://www.ncbi.nlm.nih.gov/pubmed/36047766 http://dx.doi.org/10.1002/mus.27714 |
Ejemplares similares
-
Role of NCKAP1 in the Defective Phagocytic Function of Microglia-Like Cells Derived from Rapidly Progressing Sporadic ALS
por: Noh, Min-Young, et al.
Publicado: (2023) -
Clinical and genetic characteristics of amyotrophic lateral sclerosis patients with ANXA11 variants
por: Sung, Wonjae, et al.
Publicado: (2022) -
Misdiagnosis: Hypoglossal palsy mimicking bulbar onset amyotrophic lateral sclerosis
por: Goldstein, Eric D., et al.
Publicado: (2018) -
A De Novo
RAPGEF2 Variant Identified in a Sporadic Amyotrophic Lateral Sclerosis Patient Impairs Microtubule Stability and Axonal Mitochondria Distribution
por: Heo, Keunjung, et al.
Publicado: (2018) -
Mutation in gelsolin gene in Finnish hereditary amyloidosis
Publicado: (1990)