Found: 13
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Copy Number Variation in Familial Parkinson Disease.
- Published in:
- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0020988
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- Publication type:
- Article
Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
- Published in:
- Human Genetics, 2009, v. 124, n. 6, p. 593, doi. 10.1007/s00439-008-0582-9
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- Publication type:
- Article
Novel recruitment strategy to enrich for LRRK2 mutation carriers.
- Published in:
- Molecular Genetics & Genomic Medicine, 2015, v. 3, n. 5, p. 404, doi. 10.1002/mgg3.151
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- Publication type:
- Article
Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 20, p. 2599, doi. 10.1093/hmg/ddg270
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- Publication type:
- Article
Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease.
- Published in:
- Movement Disorders, 2011, v. 26, n. 11, p. 2039, doi. 10.1002/mds.23781
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- Publication type:
- Article
Alpha-synuclein and familial Parkinson's disease.
- Published in:
- Movement Disorders, 2009, v. 24, n. 8, p. 1125, doi. 10.1002/mds.22524
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- Publication type:
- Article
Clinical correlates of depressive symptoms in familial Parkinson's disease.
- Published in:
- Movement Disorders, 2008, v. 23, n. 15, p. 2216, doi. 10.1002/mds.22285
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- Publication type:
- Article
R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation.
- Published in:
- 2007
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- Publication type:
- journal article
Mutations in LRRK2 other than G2019S are rare in a north american-based sample of familial Parkinson's disease.
- Published in:
- Movement Disorders, 2006, v. 21, n. 12, p. 2257, doi. 10.1002/mds.21162
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- Publication type:
- Article
Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia.
- Published in:
- Movement Disorders, 2006, v. 21, n. 1, p. 45, doi. 10.1002/mds.20663
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- Publication type:
- Article
Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease.
- Published in:
- Movement Disorders, 2004, v. 19, n. 6, p. 649, doi. 10.1002/mds.20097
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- Publication type:
- Article
Reliability of reported age at onset for Parkinson's disease.
- Published in:
- 2003
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- Publication type:
- journal article
Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease.
- Published in:
- BMC Medical Genetics, 2010, v. 11, p. 53, doi. 10.1186/1471-2350-11-53
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- Publication type:
- Article