Found: 6
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Lack of evidence for an association between UCHL1 S18Y and Parkinson’s disease.
- Published in:
- European Journal of Neurology, 2008, v. 15, n. 2, p. 134, doi. 10.1111/j.1468-1331.2007.02012.x
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- Article
parkin mutation dosage and the phenomenon of anticipation: a molecular genetic study of familial parkinsonism.
- Published in:
- BMC Neurology, 2005, v. 5, p. 1, doi. 10.1186/1471-2377-5-4
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- Article
Exploring gene-environment interactions in Parkinson’s disease.
- Published in:
- Human Genetics, 2008, v. 123, n. 3, p. 257, doi. 10.1007/s00439-008-0466-z
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- Article
Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.
- Published in:
- Annals of Neurology, 2007, v. 62, n. 2, p. 137, doi. 10.1002/ana.21157
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- Article
Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients.
- Published in:
- Annals of Neurology, 2007, v. 61, n. 1, p. 47, doi. 10.1002/ana.21039
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- Article
Combined effects of smoking, coffee, and NSAIDs on Parkinson's disease risk.
- Published in:
- Movement Disorders, 2008, v. 23, n. 1, p. 88, doi. 10.1002/mds.21782
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- Article