Showing results (171-180 of 761) with videos related to
Sort By:
Pageof 77
Medrxiv : the Preprint Server for Health Sciences|July 10, 2026
LRRK2 in Focus: A Global Browser Linking Genetic Diversity to Functional EffectsSpencer M Grant, Vesna van Midden, Elias Fernandez-Toledo, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 4, 2010
Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia seriesJoyce van de Leemput, Fabienne Wavrant-De Vrièze, Ian Rafferty, et al.Neuroscience Letters|May 25, 2005
Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's diseaseJavier Simon-Sanchez, Melissa Hanson, Amanda Singleton, et al.Journal of Neuropathology and Experimental Neurology|June 20, 2019
Coexistence of Progressive Supranuclear Palsy With Pontocerebellar Atrophy and Myotonic Dystrophy Type 1Shunsuke Koga, J Eric Ahlskog, Michael A DeTure, et al.Acta Neuropathologica|December 1, 2025
Genetic factors and comorbid pathologies interact to drive regional mitophagy alterations in Lewy body dementiaXu Hou, Tyrique Richardson, Michael G Heckman, et al.Neurology|November 8, 2014
LRRK2 exonic variants and risk of multiple system atrophyMichael G Heckman, Lucia Schottlaender, Alexandra I Soto-Ortolaza, et al.Journal of Neurology|November 13, 2010
Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9pJustin P Pearson, Nigel M Williams, Elisa Majounie, et al.Journal of Medical Genetics|December 1, 2019
Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson's diseaseHampton Leonard, Cornelis Blauwendraat, Lynne Krohn, et al.Parkinsonism & Related Disorders|October 15, 2017
Genetic risk factors in Finnish patients with Parkinson's diseaseSusanna Ylönen, Ari Siitonen, Michael A Nalls, et al.Parkinsonism & Related Disorders|September 24, 2009
Histamine N-methyltransferase Thr105Ile is not associated with Parkinson's disease or essential tremorBrett H Keeling, Carles Vilariño-Güell, Alexandra I Soto-Ortolaza, et al.Pageof 77