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- 2011
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Mark
Heredity in Parkinson's disease. From rare mutations to common genetic risk factors.
(
- Thesis › Doctoral thesis (compilation)
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Mark
Diagnosis and Treatment of Common Forms of Tremor
(
- Contribution to journal › Article
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Mark
Independent and Joint Effects of the MAPT and SNCA Genes in Parkinson Disease
(
- Contribution to journal › Article
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Mark
VPS35 Mutations in Parkinson Disease
(
- Contribution to journal › Article
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Mark
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study
(
- Contribution to journal › Article
-
Mark
Human leukocyte antigen variation and Parkinson's disease.
(
- 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