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- 2011
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Mark
VPS35 Mutations in Parkinson Disease
(
- Contribution to journal › Article
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Mark
Human leukocyte antigen variation and Parkinson's disease.
(
- 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
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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
- 2009
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Mark
A Swedish family with de novo alpha-synuclein A53T mutation: Evidence for early cortical dysfunction.
(
- Contribution to journal › Article
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Mark
Herman Lundborg did not describe Unverricht-Lundborg disease: hyperekplexia in a Swedish family with hereditary Parkinson's disease due to alpha-synuclein multiplications
2009) 13th Congress of the European-Federation-of-Neurological-Societies In European Journal of Neurology 16. p.153-153(
- Contribution to journal › Published meeting abstract
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Mark
Unverricht-Lundborg disease-A misnomer?
(
- Contribution to journal › Letter