Better survival in female SOD1-mutant patients with ALS: a study of SOD1-related natural history
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Title
Better survival in female SOD1-mutant patients with ALS: a study of SOD1-related natural history
Authors
Keywords
Amyotrophic lateral sclerosis, Natural history studies, <em class="EmphasisTypeItalic ">SOD1</em> mutations, Gender difference
Journal
Translational Neurodegeneration
Volume 8, Issue 1, Pages -
Publisher
Springer Nature
Online
2019-01-09
DOI
10.1186/s40035-018-0142-8
References
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Note: Only part of the references are listed.- CSF neurofilament proteins as diagnostic and prognostic biomarkers for amyotrophic lateral sclerosis
- (2018) Daniela Rossi et al. JOURNAL OF NEUROLOGY
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- (2018) Michael Benatar et al. NEUROLOGY
- A case-control study of hormonal exposures as etiologic factors for ALS in women
- (2017) James P.K. Rooney et al. NEUROLOGY
- Analysis of SOD1 mutations in a Chinese population with amyotrophic lateral sclerosis: a case-control study and literature review
- (2017) QianQian Wei et al. Scientific Reports
- Prognostic factors for survival in patients with amyotrophic lateral sclerosis: analysis of a multi-centre clinical trial
- (2016) Emma Yates et al. JOURNAL OF CLINICAL NEUROSCIENCE
- Defining SOD1 ALS natural history to guide therapeutic clinical trial design
- (2016) Taha Bali et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- H46R SOD1 mutation is consistently associated with a relatively benign form of amyotrophic lateral sclerosis with slow progression
- (2016) Zhang-Yu Zou et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- 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
- Natural history and clinical features of sporadic amyotrophic lateral sclerosis in China
- (2015) Lu Chen et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Genotype-phenotype relationship in hereditary amyotrophic lateral sclerosis
- (2015) Satoshi Yamashita et al. Translational Neurodegeneration
- Plasma neurofilament heavy chain levels and disease progression in amyotrophic lateral sclerosis: insights from a longitudinal study
- (2014) Ching-Hua Lu et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Extensive molecular genetic survey of Taiwanese patients with amyotrophic lateral sclerosis
- (2014) Bing-Wen Soong et al. NEUROBIOLOGY OF AGING
- Clinical and genetic heterogeneity of amyotrophic lateral sclerosis
- (2013) M Sabatelli et al. CLINICAL GENETICS
- An antisense oligonucleotide against SOD1 delivered intrathecally for patients with SOD1 familial amyotrophic lateral sclerosis: a phase 1, randomised, first-in-man study
- (2013) Timothy M Miller et al. LANCET NEUROLOGY
- C9orf72 repeat expansions are not detected in Chinese patients with familial ALS
- (2013) Rong Liu et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Familial amyotrophic lateral sclerosis in Alberta, Canada
- (2013) Ted Pfister et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- ALSoD: A user-friendly online bioinformatics tool for amyotrophic lateral sclerosis genetics
- (2012) Olubunmi Abel et al. HUMAN MUTATION
- Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients
- (2012) Afagh Alavi et al. NEUROBIOLOGY OF AGING
- Screening for C9orf72 repeat expansions in Chinese amyotrophic lateral sclerosis patients
- (2012) Zhang-Yu Zou et al. NEUROBIOLOGY OF AGING
- SQSTM1 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
- (2011) Faisal Fecto ARCHIVES OF NEUROLOGY
- Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
- (2011) Mariely DeJesus-Hernandez et al. NEURON
- A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
- (2011) Alan E. Renton et al. NEURON
- Association of smoking with amyotrophic lateral sclerosis risk and survival in men and women: a prospective study
- (2010) Alvaro Alonso et al. BMC Neurology
- Mutations of optineurin in amyotrophic lateral sclerosis
- (2010) Hirofumi Maruyama et al. NATURE
- Smoking may be considered an established risk factor for sporadic ALS
- (2009) C. Armon NEUROLOGY
- Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
- (2009) C. Vance et al. SCIENCE
- SOD1 gene mutations in ALS patients from British Columbia, Canada: Clinical features, neurophysiology and ethical issues in management
- (2008) Andrew Eisen et al. Amyotrophic Lateral Sclerosis
- Survival rate of patients with amyotrophic lateral sclerosis in Wakayama Prefecture, Japan, 1966 to 2005
- (2008) Tameko Kihira et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis
- (2008) Vivianna M Van Deerlin et al. LANCET NEUROLOGY
- TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
- (2008) Edor Kabashi et al. NATURE GENETICS
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