Found: 12
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A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 8, p. 2220
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- Publication type:
- Article
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis.
- Published in:
- Nature, 2012, v. 488, n. 7412, p. 499, doi. 10.1038/nature11280
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- Publication type:
- Article
Elevated Global DNA Methylation Is Not Exclusive to Amyotrophic Lateral Sclerosis and Is Also Observed in Spinocerebellar Ataxia Types 1 and 2.
- Published in:
- Neurodegenerative Diseases, 2018, v. 18, n. 1, p. 38, doi. 10.1159/000486201
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- Publication type:
- Article
Correction to: Motor, cognitive and behavioural profiles of C9orf72 expansion-related amyotrophic lateral sclerosis.
- Published in:
- 2023
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- Publication type:
- Correction Notice
Motor, cognitive and behavioural profiles of C9orf72 expansion-related amyotrophic lateral sclerosis.
- Published in:
- Journal of Neurology, 2023, v. 270, n. 2, p. 898, doi. 10.1007/s00415-022-11433-z
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- Publication type:
- Article
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations.
- Published in:
- 2015
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- Publication type:
- Letter
Oligoclonal bands in the cerebrospinal fluid of amyotrophic lateral sclerosis patients with disease-associated mutations.
- Published in:
- Journal of Neurology, 2013, v. 260, n. 1, p. 85, doi. 10.1007/s00415-012-6589-0
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- Publication type:
- Article
PON1 is a disease modifier gene in amyotrophic lateral sclerosis: association of the Q192R polymorphism with bulbar onset and reduced survival.
- Published in:
- 2019
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- Publication type:
- journal article
TARDBP mutations in a cohort of Italian patients with Parkinson’s disease and atypical parkinsonisms.
- Published in:
- Frontiers in Aging Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnagi.2022.1020948
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- Publication type:
- Article
The role of de novo mutations in the development of amyotrophic lateral sclerosis.
- Published in:
- Human Mutation, 2017, v. 38, n. 11, p. 1534, doi. 10.1002/humu.23295
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- Publication type:
- Article
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.
- Published in:
- JAMA Neurology, 2016, v. 73, n. 7, p. 812, doi. 10.1001/jamaneurol.2016.1114
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- Publication type:
- Article
The LRRK2 Variant E193K Prevents Mitochondrial Fission Upon MPP+ Treatment by Altering LRRK2 Binding to DRP1.
- Published in:
- Frontiers in Molecular Neuroscience, 2018, p. 1, doi. 10.3389/fnmol.2018.00064
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- Publication type:
- Article