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Movement Disorders : Official Journal of the Movement Disorder Society
|
October 27, 2005
Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics
Denise M Kay, Cyrus P Zabetian, Stewart A Factor, et al.
Parkinson'S Disease
|
December 6, 2018
Diagnostic Validation for Participants in the Washington State Parkinson Disease Registry
Hojoong M Kim, James B Leverenz, Daniel J Burdick, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 11, 2012
Risk prediction for complex diseases: application to Parkinson disease
Taryn O Hall, Jia Y Wan, Ignacio F Mata, et al.
Parkinsonism & Related Disorders
|
October 26, 2013
Association mapping of the PARK10 region for Parkinson's disease susceptibility genes
Jia Y Wan, Karen L Edwards, Carolyn M Hutter, et al.
Annals of Neurology
|
May 16, 2007
DBH -1021C-->T does not modify risk or age at onset in Parkinson's disease
Lani S Chun, Ali Samii, Carolyn M Hutter, et al.
Archives of Neurology
|
March 12, 2008
Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders
Ignacio F Mata, Ali Samii, Seth H Schneer, et al.
Human Genetics
|
January 23, 2008
Exploring gene-environment interactions in Parkinson's disease
Colin C McCulloch, Denise M Kay, Stewart A Factor, et al.
Genetic Testing
|
October 6, 2006
Validity and utility of a LRRK2 G2019S mutation test for the diagnosis of Parkinson's disease
Denise M Kay, Tom D Bird, Cyrus P Zabetian, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 15, 2010
A novel X-linked four-repeat tauopathy with Parkinsonism and spasticity
Parvoneh Poorkaj, Wendy H Raskind, James B Leverenz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 8, 2007
Combined effects of smoking, coffee, and NSAIDs on Parkinson's disease risk
Karen M Powers, Denise M Kay, Stewart A Factor, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 89) with videos related to
Sort By:
Page
of 9
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 27, 2005
Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics
Denise M Kay, Cyrus P Zabetian, Stewart A Factor, et al.
Parkinson'S Disease
|
December 6, 2018
Diagnostic Validation for Participants in the Washington State Parkinson Disease Registry
Hojoong M Kim, James B Leverenz, Daniel J Burdick, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 11, 2012
Risk prediction for complex diseases: application to Parkinson disease
Taryn O Hall, Jia Y Wan, Ignacio F Mata, et al.
Parkinsonism & Related Disorders
|
October 26, 2013
Association mapping of the PARK10 region for Parkinson's disease susceptibility genes
Jia Y Wan, Karen L Edwards, Carolyn M Hutter, et al.
Annals of Neurology
|
May 16, 2007
DBH -1021C-->T does not modify risk or age at onset in Parkinson's disease
Lani S Chun, Ali Samii, Carolyn M Hutter, et al.
Archives of Neurology
|
March 12, 2008
Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders
Ignacio F Mata, Ali Samii, Seth H Schneer, et al.
Human Genetics
|
January 23, 2008
Exploring gene-environment interactions in Parkinson's disease
Colin C McCulloch, Denise M Kay, Stewart A Factor, et al.
Genetic Testing
|
October 6, 2006
Validity and utility of a LRRK2 G2019S mutation test for the diagnosis of Parkinson's disease
Denise M Kay, Tom D Bird, Cyrus P Zabetian, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 15, 2010
A novel X-linked four-repeat tauopathy with Parkinsonism and spasticity
Parvoneh Poorkaj, Wendy H Raskind, James B Leverenz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 8, 2007
Combined effects of smoking, coffee, and NSAIDs on Parkinson's disease risk
Karen M Powers, Denise M Kay, Stewart A Factor, et al.
Page
of 9