Found: 9
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Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease.
- Published in:
- Acta Neuropathologica Communications, 2021, v. 9, n. 1, p. 1, doi. 10.1186/s40478-021-01121-w
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- Article
P3-159: MAPT H1 subhaplotyping in european PD association samples implicates tau splicing in early-onset parkinson’s disease susceptibility
- Published in:
- 2006
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- Publication type:
- Abstract
P3-159: MAPT H1 subhaplotyping in european PD association samples implicates tau splicing in early-onset parkinson’s disease susceptibility
- Published in:
- 2006
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- Abstract
Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients.
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- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 471, doi. 10.1038/sj.ejhg.5201986
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- Article
Recreational use of nitrous oxide may cause collateral neurological damage.
- Published in:
- 2021
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- Publication type:
- Letter
α‐Synuclein promoter confers susceptibility to Parkinson's disease.
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- Annals of Neurology, 2004, v. 56, n. 4, p. 591, doi. 10.1002/ana.20268
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- Article
Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export.
- Published in:
- Acta Neuropathologica, 2020, v. 139, n. 6, p. 1001, doi. 10.1007/s00401-020-02145-7
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- Article
Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population.
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- Human Mutation, 2009, v. 30, n. 7, p. 1054, doi. 10.1002/humu.21007
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- Article
Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease.
- Published in:
- Human Mutation, 2008, v. 29, n. 6, p. 832, doi. 10.1002/humu.20713
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- Publication type:
- Article