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Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2013
Primary dystonia: moribund or viableSusan B Bressman, Rachel Saunders-Pullman
Gender Medicine|June 14, 2011
Diagnosis and referral delay in women with Parkinson's diseaseRachel Saunders-Pullman, Cuiling Wang, Kaili Stanley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 13, 2009
Responsiveness to levodopa in epsilon-sarcoglycan deletionsMarta San Luciano, Laurie Ozelius, Katherine Sims, et al.
The Lancet. Neurology|April 7, 2009
Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening studySusan B Bressman, Deborah Raymond, Tania Fuchs, 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.
Annals of Clinical and Translational Neurology|December 11, 2014
Olfactory identification in LRRK2 G2019S mutation carriers: a relevant marker?Rachel Saunders-Pullman, Anat Mirelman, Cuiling Wang, et al.
Nature Genetics|February 3, 2009
Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystoniaTania Fuchs, Sophie Gavarini, Rachel Saunders-Pullman, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|February 27, 2013
Spatial Discrimination Threshold Abnormalities are not Detected in a Pilot Study of DYT6 Dystonia Mutation CarriersAndres F Deik, Sean O'Riordan, Marta San Luciano, 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.
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