The distinct manifestation of young-onset amyotrophic lateral sclerosis in China
Published 2020 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
The distinct manifestation of young-onset amyotrophic lateral sclerosis in China
Authors
Keywords
-
Journal
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Volume -, Issue -, Pages 1-8
Publisher
Informa UK Limited
Online
2020-07-30
DOI
10.1080/21678421.2020.1797091
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Clinical and genetic features of patients with amyotrophic lateral sclerosis in southern China
- (2020) W. Chen et al. EUROPEAN JOURNAL OF NEUROLOGY
- Genetics of amyotrophic lateral sclerosis: A review
- (2019) Stéphane Mathis et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- Unbiased MRI Analyses Identify Micropathologic Differences Between Upper Motor Neuron-Predominant ALS Phenotypes
- (2019) Venkateswaran Rajagopalan et al. Frontiers in Neuroscience
- Novel and Recurrent Mutations in a Cohort of Chinese Patients With Young-Onset Amyotrophic Lateral Sclerosis
- (2019) Jianwen Deng et al. Frontiers in Neuroscience
- The epidemiology and genetics of Amyotrophic lateral sclerosis in China
- (2018) Xiaolu Liu et al. BRAIN RESEARCH
- Age-specific ALS incidence: a dose–response meta-analysis
- (2018) Benoît Marin et al. EUROPEAN JOURNAL OF EPIDEMIOLOGY
- ALS Genes in the Genomic Era and their Implications for FTD
- (2018) Hung Phuoc Nguyen et al. TRENDS IN GENETICS
- Clinical presentation and natural history of infantile-onset ascending spastic paralysis from three families with an ALS2 founder variant
- (2018) Mayada Helal et al. NEUROLOGICAL SCIENCES
- Genetics insight into the amyotrophic lateral sclerosis/frontotemporal dementia spectrum
- (2017) Ai-Ling Ji et al. JOURNAL OF MEDICAL GENETICS
- Genetic epidemiology of amyotrophic lateral sclerosis: a systematic review and meta-analysis
- (2017) Zhang-Yu Zou et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Amyotrophic lateral sclerosis
- (2017) Michael A van Es et al. LANCET
- Amyotrophic Lateral Sclerosis
- (2017) Robert H. Brown et al. NEW ENGLAND JOURNAL OF MEDICINE
- REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants
- (2016) Nilah M. Ioannidis et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A rapid functional decline type of amyotrophic lateral sclerosis is linked to low expression ofTTN
- (2016) Hazuki Watanabe et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Mutations in FUS are the most frequent genetic cause in juvenile sporadic ALS patients of Chinese origin
- (2016) Zhang-Yu Zou et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Clinical and demographic factors and outcome of amyotrophic lateral sclerosis in relation to population ancestral origin
- (2015) Benoît Marin et al. EUROPEAN JOURNAL OF EPIDEMIOLOGY
- Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
- (2015) Sue Richards et al. GENETICS IN MEDICINE
- The distinctive genetic architecture of ALS in mainland China: Table 1
- (2015) Zhang-Yu Zou et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Natural history and clinical features of sporadic amyotrophic lateral sclerosis in China
- (2015) Lu Chen et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes
- (2014) Janet Cady et al. ANNALS OF NEUROLOGY
- The PRO-ACT database: Design, initial analyses, and predictive features
- (2014) N. Atassi et al. NEUROLOGY
- Age at onset of amyotrophic lateral sclerosis in China
- (2013) M. S. Liu et al. ACTA NEUROLOGICA SCANDINAVICA
- Interaction between AP-5 and the hereditary spastic paraplegia proteins SPG11 and SPG15
- (2013) Jennifer Hirst et al. MOLECULAR BIOLOGY OF THE CELL
- State of play in amyotrophic lateral sclerosis genetics
- (2013) Alan E Renton et al. NATURE NEUROSCIENCE
- The epidemiology of ALS: a conspiracy of genes, environment and time
- (2013) Ammar Al-Chalabi et al. Nature Reviews Neurology
- Young-onset amyotrophic lateral sclerosis: historical and other observations
- (2012) M. R. Turner et al. BRAIN
- A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis
- (2011) Amr Al-Saif et al. ANNALS OF NEUROLOGY
- Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study
- (2011) A. Chio et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
- (2011) Han-Xiang Deng et al. NATURE
- FUS mutations in sporadic amyotrophic lateral sclerosis: Clinical and genetic analysis
- (2011) William Sproviero et al. NEUROBIOLOGY OF AGING
- Exome sequencing reveals SPG11 mutations causing juvenile ALS
- (2011) Hussein Daoud et al. NEUROBIOLOGY OF AGING
- Clinical features that distinguish PLS, upper motor neuron-dominant ALS, and typical ALS
- (2009) P. H. Gordon et al. NEUROLOGY
- Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
- (2009) T. J. Kwiatkowski et al. SCIENCE
- Natural history of young-adult amyotrophic lateral sclerosis
- (2008) M. Sabatelli et al. NEUROLOGY
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started