Found: 9
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SMPD1 mutations, activity, and α-synuclein accumulation in Parkinson's disease.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Teneurin transmembrane protein 4 is not a cause for essential tremor in a Canadian population.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Oligogenicity, C9orf72 expansion, and variant severity in ALS.
- Published in:
- Neurogenetics, 2020, v. 21, n. 3, p. 227, doi. 10.1007/s10048-020-00612-7
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- Publication type:
- Article
Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Genetic, Structural, and Functional Evidence Link TMEM175 to Synucleinopathies.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Absence of Mutation Enrichment for Genes Phylogenetically Conserved in the Olivocerebellar Motor Circuitry in a Cohort of Canadian Essential Tremor Cases.
- Published in:
- Molecular Neurobiology, 2019, v. 56, n. 6, p. 4317, doi. 10.1007/s12035-018-1369-1
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- Publication type:
- Article
Comprehensive Analysis of Familial Parkinsonism Genes in Rapid-Eye-Movement Sleep Behavior Disorder.
- Published in:
- 2021
- By:
- Publication type:
- journal article
CCM2 mutations account for 13% of cases in a large collection of kindreds with hereditary cavernous malformations.
- Published in:
- Annals of Neurology, 2004, v. 55, n. 5, p. 757
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- Publication type:
- Article