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Movement Disorders : Official Journal of the Movement Disorder Society|July 16, 2004
Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutationsLorraine N Clark, Shehla Afridi, Helen Mejia-Santana, et al.Neuro-Degenerative Diseases|August 30, 2017
Two Ethnic Clusters with Huntington Disease in Israel: The Case of Mountain Jews and KaraitesJennifer Zitser, Avner Thaler, Noit Inbar, et al.NPJ Parkinson'S Disease|April 26, 2016
SCARB2 variants and glucocerebrosidase activity in Parkinson's diseaseRoy N Alcalay, Oren A Levy, Pavlina Wolf, et al.Brain : a Journal of Neurology|June 29, 2015
Glucocerebrosidase activity in Parkinson's disease with and without GBA mutationsRoy N Alcalay, Oren A Levy, Cheryl C Waters, et al.Journal of Neurology|September 5, 2021
COVID-19 manifestations in people with Parkinson's disease: a USA cohortYaqian Xu, Matthew Surface, Amanda K Chan, et al.Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|September 25, 2014
Evidence that formulations of the selective MAO-B inhibitor, selegiline, which bypass first-pass metabolism, also inhibit MAO-A in the human brainJoanna S Fowler, Jean Logan, Nora D Volkow, et al.Plos One|May 2, 2015
Gene-wise association of variants in four lysosomal storage disorder genes in neuropathologically confirmed Lewy body diseaseLorraine N Clark, Robin Chan, Rong Cheng, et al.European Journal of Medical Genetics|May 30, 2018
Increased yield of full GBA sequencing in Ashkenazi Jews with Parkinson's diseaseJennifer A Ruskey, Lior Greenbaum, Léanne Roncière, et al.Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|November 28, 2013
Designing clinical trials for dystoniaWendy R Galpern, Christopher S Coffey, Alberto Albanese, et al.Frontiers in Molecular Neuroscience|September 19, 2024
A novel super-resolution microscopy platform for cutaneous alpha-synuclein detection in Parkinson's diseaseOfir Sade, Daphna Fischel, Noa Barak-Broner, et al.Pageof 17