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Annals of Clinical and Translational Neurology|January 20, 2016
Psychiatric disorders, myoclonus dystonia and SGCE: an international studyKathryn J Peall, Joke M Dijk, Rachel Saunders-Pullman, et al.Annals of Neurology|October 1, 1996
Exclusion of the DYT1 locus in familial torticollisS B Bressman, T T Warner, L Almasy, et al.Archives of Neurology|September 16, 2009
Occupation and risk of parkinsonism: a multicenter case-control studyCaroline M Tanner, G Webster Ross, Sarah A Jewell, et al.Nature Genetics|September 1, 1997
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding proteinL J Ozelius, J W Hewett, C E Page, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Distribution, type, and origin of Parkin mutations: review and case studiesKatja Hedrich, Cordula Eskelson, Beth Wilmot, et al.Nature Genetics|December 11, 2012
Mutations in GNAL cause primary torsion dystoniaTania Fuchs, Rachel Saunders-Pullman, Ikuo Masuho, et al.Movement Disorders : Official Journal of the Movement Disorder Society|April 1, 2018
Application of the Movement Disorder Society prodromal criteria in healthy G2019S-LRRK2 carriersAnat Mirelman, Rachel Saunders-Pullman, Roy N Alcalay, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 15, 2015
REM sleep behavior disorder, as assessed by questionnaire, in G2019S LRRK2 mutation PD and carriersRachel Saunders-Pullman, Roy N Alcalay, Anat Mirelman, et al.Journal of the Neurological Sciences|October 25, 2016
Neuropsychiatric characteristics of GBA-associated Parkinson diseaseMatthew Swan, Nancy Doan, Robert A Ortega, et al.Human Genetics|April 30, 2018
High-depth whole genome sequencing of an Ashkenazi Jewish reference panel: enhancing sensitivity, accuracy, and imputationTodd Lencz, Jin Yu, Cameron Palmer, et al.Pageof 30