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Annals of Neurology|January 3, 2013
Mutations in KCND3 cause spinocerebellar ataxia type 22Yi-Chung Lee, Alexandra Durr, Karen Majczenko, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 29, 2009
Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: large-scale collaborative studyEvangelos Evangelou, Demetrius M Maraganore, Grazia Annesi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 15, 2020
Nonsteroidal Anti-inflammatory Use and LRRK2 Parkinson's Disease PenetranceMarta San Luciano, Caroline M Tanner, Cheryl Meng, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 5, 2021
Plasma NfL levels and longitudinal change rates in C9orf72 and GRN-associated diseases: from tailored references to clinical applicationsDario Saracino, Karim Dorgham, Agnès Camuzat, et al.
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.
Archives of Neurology|October 10, 2007
Asian origin for the worldwide-spread mutational event in Machado-Joseph diseaseSandra Martins, Francesc Calafell, Claudia Gaspar, et al.
Human Mutation|April 17, 2007
Progranulin null mutations in both sporadic and familial frontotemporal dementiaIsabelle Le Ber, Julie van der Zee, Didier Hannequin, et al.
Ebiomedicine|May 30, 2025
Impact of Y chromosome loss on the risk of Parkinson's disease and progressionJunhao Wang, Xinyi Chen, Wenxuan Du, et al.
Orphanet Journal of Rare Diseases|October 30, 2013
Phenotypic variability in ARCA2 and identification of a core ataxic phenotype with slow progressionCyril Mignot, Emmanuelle Apartis, Alexandra Durr, et al.
Annals of Neurology|October 5, 2012
Adult polyglucosan body disease: Natural History and Key Magnetic Resonance Imaging FindingsFanny Mochel, Raphael Schiffmann, Marjan E Steenweg, et al.
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