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- 2011
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Mark
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study
(
- Contribution to journal › Article
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Mark
An African-American family with dystonia.
(
- Contribution to journal › Article
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Mark
A family with parkinsonism, essential tremor, restless legs syndrome, and depression
(
- Contribution to journal › Article
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Mark
A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease
(
- Contribution to journal › Article
- 2010
-
Mark
Hereditary Parkinson's Disease of Unknown Genetic Cause in Two Families from Southern Sweden
2010) 24th Annual Symposium on Etiology, Pathogenesis and Treatment of Parkinsons Disease and Other Movement Disorders In Movement Disorders 25(6).(
- Contribution to journal › Published meeting abstract
-
Mark
LRRK2 variation and Parkinson's disease in African Americans
(
- Contribution to journal › Article
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Mark
Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease : large-scale collaborative study
(
- Contribution to journal › Article
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Mark
Familial late-onset focal dystonia in an African American family
(
- Contribution to journal › Published meeting abstract