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Journal of the International Neuropsychological Society : JINS|November 25, 2010
Neuropsychological Profile of Parkin Mutation Carriers with and without Parkinson Disease: The CORE-PD StudyElise Caccappolo, Roy N Alcalay, Helen Mejia-Santana, et al.Archives of Neurology|June 19, 2010
Predictors of parkin mutations in early-onset Parkinson disease: the consortium on risk for early-onset Parkinson disease studyKaren S Marder, Ming X Tang, Helen Mejia-Santana, et al.JAMA Neurology|November 6, 2013
Cognitive and motor function in long-duration PARKIN-associated Parkinson diseaseRoy N Alcalay, Elise Caccappolo, Helen Mejia-Santana, et al.Brain : a Journal of Neurology|July 29, 2024
Parkinson's disease variant detection and disclosure: PD GENEration, a North American studyLola Cook, Jennifer Verbrugge, Tae-Hwi Schwantes-An, et al.Cell Reports|July 27, 2012
Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsionsHsien-Yang Lee, Yong Huang, Nadine Bruneau, et al.Plos Genetics|March 14, 2012
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility lociEimear E Kenny, Itsik Pe'er, Amir Karban, et al.Movement Disorders : Official Journal of the Movement Disorder Society|November 19, 2013
Parkinson disease phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutationsRoy N Alcalay, Anat Mirelman, Rachel Saunders-Pullman, et al.Science Translational Medicine|January 12, 2018
Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's diseaseKen Y Hui, Heriberto Fernandez-Hernandez, Jianzhong Hu, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 17, 2024
Genetic Risk Factors in Isolated Dystonia Escape Genome-Wide Association StudiesBjörn-Hergen Laabs, Katja Lohmann, Eva-Juliane Vollstedt, et al.Annals of Neurology|May 3, 2021
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's DiseaseDongbing Lai, Babak Alipanahi, Pierre Fontanillas, et al.Pageof 30