Showing results (221-230 of 291) with videos related to

Sort By:
Pageof 30
American Journal of Medical Genetics. Part A|August 21, 2007
Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the Amish-MennonitesRachel Saunders-Pullman, Deborah Raymond, Geetha Senthil, et al.
JAMA Network Open|April 21, 2021
Association of Dual LRRK2 G2019S and GBA Variations With Parkinson Disease ProgressionRoberto A Ortega, Cuiling Wang, Deborah Raymond, et al.
Neurology|February 12, 2004
Mutations in DYT1: extension of the phenotypic and mutational spectrumK Kabakci, K Hedrich, J C Leung, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|October 17, 2008
Research priorities in spasmodic dysphoniaChristy L Ludlow, Charles H Adler, Gerald S Berke, et al.
Neurology|March 29, 2013
The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson diseaseZiv Gan-Or, Laurie J Ozelius, Anat Bar-Shira, et al.
Neurology|February 12, 2004
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson diseaseK Hedrich, A Djarmati, N Schäfer, et al.
JMIR Cancer|April 30, 2024
Implementation of Health IT for Cancer Screening in US Primary Care: Scoping ReviewConstance Owens-Jasey, Jinying Chen, Ran Xu, et al.
JAMA Neurology|January 9, 2018
Progression in the LRRK2-Asssociated Parkinson Disease PopulationRachel Saunders-Pullman, Anat Mirelman, Roy N Alcalay, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 17, 1999
Primary torsion dystonia: the search for genes is not overP R Jarman, N del Grosso, E M Valente, et al.
Neurology|February 21, 2012
Variant ataxia-telangiectasia presenting as primary-appearing dystonia in Canadian MennonitesR Saunders-Pullman, D Raymond, A J Stoessl, et al.
Pageof 30