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Journal of the National Cancer Institute|December 20, 2015
PARKIN Inactivation Links Parkinson's Disease to MelanomaHui-Han Hu, Caroline Kannengiesser, Suzanne Lesage, et al.Frontiers in Cellular Neuroscience|May 4, 2023
C9ORF72 knockdown triggers FTD-like symptoms and cell pathology in miceMaria-Belen Lopez-Herdoiza, Stephanie Bauché, Baptiste Wilmet, et al.Brain : a Journal of Neurology|March 27, 2015
PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxiaRebekah K Jobling, Mirna Assoum, Oleksandr Gakh, et al.American Journal of Human Genetics|February 7, 2012
RAD51 haploinsufficiency causes congenital mirror movements in humansChristel Depienne, Delphine Bouteiller, Aurélie Méneret, et al.Brain : a Journal of Neurology|May 15, 2009
CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5Cyril Goizet, Amir Boukhris, Alexandra Durr, et al.Brain : a Journal of Neurology|December 20, 2021
Motor neuron pathology in CANVAS due to RFC1 expansionsVincent Huin, Giulia Coarelli, Clément Guemy, et al.Neurobiology of Aging|February 6, 2018
Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's diseaseCornelis Blauwendraat, Demis A Kia, Lasse Pihlstrøm, et al.Journal of Alzheimer'S Disease : JAD|September 25, 2015
Lateral Temporal Lobe: An Early Imaging Marker of the Presymptomatic GRN Disease?Paola Caroppo, Marie-Odile Habert, Stanley Durrleman, et al.Movement Disorders : Official Journal of the Movement Disorder Society|June 3, 2025
Genetic Analysis of the X Chromosome Associates Loci with Progression of Parkinson's DiseaseYu Liao, Hao Wu, Junhao Wang, et al.Annals of Neurology|April 5, 2016
DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseasesConceição Bettencourt, Davina Hensman-Moss, Michael Flower, et al.Pageof 50