Extensive molecular genetic survey of Taiwanese patients with amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

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Extensive molecular genetic survey of Taiwanese patients with amyotrophic lateral sclerosis

Published:2014-10 Issue:10 Volume:35 Page:2423.e1-2423.e6
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Soong Bing-Wen,Lin Kon-Ping,Guo Yuh-Cherng,Lin Chou-Ching K.,Tsai Pei-Chien,Liao Yi-Chu,Lu Yi-Chun,Wang Shuu-Jiun,Tsai Ching-Piao,Lee Yi-Chung

Funder

National Science Council Taiwan

Taipei Veterans General Hospital

Ministry of Education

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

Reference54 articles.

1. A method and server for predicting damaging missense mutations;Adzhubei;Nat. Methods,2010

2. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis;Brooks;Amyotroph. Lateral Scler. Other Motor Neuron Disord.,2000

3. SOD1, ANG, TARDBP and FUS mutations in amyotrophic lateral sclerosis: a United States clinical testing lab experience;Brown;Amyotroph. Lateral Scler.,2012

4. Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9ORF72 repeat expansion: a population-based cohort study;Byrne;Lancet Neurol.,2012

5. Ataxin-2 intermediate-length polyglutamine: a possible risk factor for Chinese patient with amyotrophic lateral sclerosis;Chen;Neurobiol. Aging,2011

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1. Variability in Clinical Phenotype in TARDBP Mutations: Amyotrophic Lateral Sclerosis Case Description and Literature Review;Genes;2023-11-04

2. Predictors for progression in amyotrophic lateral sclerosis associated to SOD1 mutation: insight from two population-based registries;Journal of Neurology;2023-09-05

3. Valosin containing protein (VCP): initiator, modifier, and potential drug target for neurodegenerative diseases;Molecular Neurodegeneration;2023-08-07

4. Respiratory onset of amyotrophic lateral sclerosis in a pregnant woman with a novel SOD1 mutation;European Journal of Neurology;2022-03-07

5. Mutation analysis of SOD1, C9orf72, TARDBP and FUS genes in ethnically-diverse Malaysian patients with amyotrophic lateral sclerosis (ALS);Neurobiology of Aging;2021-12

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