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Human Molecular Genetics|March 4, 2010
Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humansSuzanne Lesage, Etienne Patin, Christel Condroyer, et al.
Brain : a Journal of Neurology|September 8, 2022
PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disabilityChristina Fevga, Christelle Tesson, Ana Carreras Mascaro, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 3, 2021
Availability of Therapies and Services for Parkinson's Disease in Africa: A Continent-Wide SurveyEman Hamid, Biniyam A Ayele, Daniel Gams Massi, et al.
Brain : a Journal of Neurology|July 30, 2023
Neuromuscular disease genetics in under-represented populations: increasing data diversityLindsay A Wilson, William L Macken, Luke D Perry, et al.
Neurology|September 11, 2015
Large-scale assessment of polyglutamine repeat expansions in Parkinson diseaseLisa Wang, Jan O Aasly, Grazia Annesi, et al.
The Lancet. Neurology|September 3, 2011
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control studyOwen A Ross, Alexandra I Soto-Ortolaza, Michael G Heckman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 15, 2023
Cerebellar Volume and Disease Staging in Parkinson's Disease: An ENIGMA-PD StudyRebecca Kerestes, Max A Laansma, Conor Owens-Walton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 6, 2013
Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) ConsortiumMichael G Heckman, Alexandra I Soto-Ortolaza, Jan O Aasly, et al.
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