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Nature Genetics|December 11, 2012
Mutations in GNAL cause primary torsion dystoniaTania Fuchs, Rachel Saunders-Pullman, Ikuo Masuho, 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.Movement Disorders Clinical Practice|December 14, 2023
An Empirical Comparison of Commonly Used Universal Rating Scales for DystoniaDeniz Boz, Gamze Kilic-Berkmen, Joel S Perlmutter, et al.Neurology|February 27, 2020
Defining research priorities in dystoniaCodrin Lungu, Laurie Ozelius, David Standaert, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 5, 2008
Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with epsilon-sarcoglycan mutationsDeborah Raymond, Rachel Saunders-Pullman, Patricia de Carvalho Aguiar, et al.Brain : a Journal of Neurology|February 7, 2007
The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 geneAllison Brashear, William B Dobyns, Patricia de Carvalho Aguiar, et al.Movement Disorders : Official Journal of the Movement Disorder Society|November 28, 2019
Cervical dystonia incidence and diagnostic delay in a multiethnic populationSara C LaHue, Kathleen Albers, Samuel Goldman, et al.Neurology|August 22, 2022
Association of Olfactory Performance With Motor Decline and Age at Onset in People With Parkinson Disease and the LRRK2 G2019S VariantRachel Saunders-Pullman, Roberto Angel Ortega, Cuiling Wang, et al.Neuron|December 13, 2016
Functional Genomic Analyses of Mendelian and Sporadic Disease Identify Impaired eIF2α Signaling as a Generalizable Mechanism for DystoniaJoseph E Rittiner, Zachary F Caffall, Ricardo Hernández-Martinez, et al.Annals of Clinical and Translational Neurology|September 25, 2015
GBA mutations are associated with Rapid Eye Movement Sleep Behavior DisorderZiv Gan-Or, Anat Mirelman, Ronald B Postuma, et al.Pageof 13