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Movement Disorders : Official Journal of the Movement Disorder Society|May 9, 2015
Disclosure of research results in genetic studies of Parkinson's disease caused by LRRK2 mutationsClaustre Pont-Sunyer, Susan Bressman, Deborah Raymond, et al.
Annals of Clinical and Translational Neurology|November 22, 2017
Sex differences in LRRK2 G2019S and idiopathic Parkinson's DiseaseMarta San Luciano, Cuiling Wang, Roberto A Ortega, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 26, 2011
Mood and cognition in leucine-rich repeat kinase 2 G2019S Parkinson's diseaseVicki Shanker, Mark Groves, Gary Heiman, et al.
Neurology|January 4, 2013
Metabolic changes in DYT11 myoclonus-dystoniaMaren Carbon, Deborah Raymond, Laurie Ozelius, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 12, 2011
Substantia nigra hyperechogenicity with LRRK2 G2019S mutationsNorbert Brüggemann, Johann Hagenah, Kaili Stanley, et al.
Current Neurology and Neuroscience Reports|July 2, 2013
The association between ß-glucocerebrosidase mutations and parkinsonismMatthew Swan, Rachel Saunders-Pullman
Muscle & Nerve|December 12, 2013
Atypical presentation of late-onset Tay-Sachs diseaseAndres Deik, Rachel Saunders-Pullman
Neuroscience Letters|April 25, 2006
Increased frequency of the LRRK2 G2019S mutation in an elderly Ashkenazi Jewish population is not associated with dementiaRachel Saunders-Pullman, Richard B Lipton, Geetha Senthil, et al.
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