Found: 14
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Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease.
- Published in:
- 2001
- By:
- Publication type:
- journal article
Complete Genomic Screen in Parkinson Disease.
- Published in:
- JAMA: Journal of the American Medical Association, 2001, v. 286, n. 18, p. 2239, doi. 10.1001/jama.286.18.2239
- By:
- Publication type:
- Article
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy.
- Published in:
- Nature Genetics, 2012, v. 44, n. 4, p. 450, doi. 10.1038/ng.1103
- By:
- Publication type:
- Article
Pesticide exposure and risk of Parkinson's disease: A family-based case-control study.
- Published in:
- 2008
- By:
- Publication type:
- Case Study
Genome-Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease.
- Published in:
- Annals of Human Genetics, 2010, v. 74, n. 2, p. 97, doi. 10.1111/j.1469-1809.2009.00560.x
- By:
- Publication type:
- Article
NOS2A and the modulating effect of cigarette smoking in Parkinson's disease.
- Published in:
- Annals of Neurology, 2006, v. 60, n. 3, p. 366
- By:
- Publication type:
- Article
Parkin mutations and susceptibility alleles in late-onset Parkinson's disease.
- Published in:
- Annals of Neurology, 2003, v. 53, n. 5, p. 624
- By:
- Publication type:
- Article
Confirmation of linkage of oculopharyngel muscular dystrophy to chromosome 14q 11.2-q13.
- Published in:
- Annals of Neurology, 1996, v. 40, n. 5, p. 801, doi. 10.1002/ana.410400519
- By:
- Publication type:
- Article
Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype.
- Published in:
- Neurogenetics, 2004, v. 5, n. 3, p. 147, doi. 10.1007/s10048-004-0180-5
- By:
- Publication type:
- Article
Linkage of familial essential tremor to chromosome 5q35.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Exclusion of Identified LGMD1 Loci from Four Dominant Limb-Girdle Muscular Dystrophy Families.
- Published in:
- Human Heredity, 1998, v. 48, n. 4, p. 179, doi. 10.1159/000022799
- By:
- Publication type:
- Article
Missense mutation in a von Willebrand factor type A domain of the α3(VI) collagen gene ( COL6A3) in a family with Bethlem myopathy.
- Published in:
- Human Molecular Genetics, 1998, v. 7, n. 5, p. 807, doi. 10.1093/hmg/7.5.807
- By:
- Publication type:
- Article
Evidence for Locus Heterogeneity in the Bethlem Myopathy and Linkage to 2q37.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 7, p. 1043, doi. 10.1093/hmg/5.7.1043
- By:
- Publication type:
- Article
The ischemic exercise test in normal adults and in patients with weakness and cramps.
- Published in:
- Muscle & Nerve, 1986, v. 9, n. 3, p. 216, doi. 10.1002/mus.880090305
- By:
- Publication type:
- Article