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Neurological Research and Practice|October 30, 2024
Iatrogenic botulism after intragastric botulinum neurotoxin injections - a major outbreakTsepo Goerttler, Martin B Dorner, Christina van der Linden, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 15, 2013
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphismStephan Klebe, Jean-Louis Golmard, Michael A Nalls, et al.The New England Journal of Medicine|September 1, 2006
A randomized trial of deep-brain stimulation for Parkinson's diseaseGünther Deuschl, Carmen Schade-Brittinger, Paul Krack, et al.Movement Disorders : Official Journal of the Movement Disorder Society|February 12, 2022
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar AtaxiaLiedewei Van de Vondel, Jonathan De Winter, Danique Beijer, et al.Brain Communications|January 4, 2024
Expanding the phenotypic spectrum of CLCN2-related leucoencephalopathy and ataxiaPaulo R Nóbrega, Anderson R B de Paiva, Katiane S Souza, et al.Brain : a Journal of Neurology|July 5, 2014
Parkinson's disease in GTP cyclohydrolase 1 mutation carriersNiccolò E Mencacci, Ioannis U Isaias, Martin M Reich, et al.Ebiomedicine|December 27, 2023
Clinical and genetic keys to cerebellar ataxia due to FGF14 GAA expansionsJean-Loup Méreaux, Claire-Sophie Davoine, David Pellerin, et al.JAMA Neurology|January 20, 2026
Virus-Specific T Cells and Response to Checkpoint Inhibitors in Progressive Multifocal LeukoencephalopathyNora Möhn, Lea Grote-Levi, Agnes Bonifacius, et al.Brain : a Journal of Neurology|November 1, 2016
Genome-wide association study in essential tremor identifies three new lociStefanie H Müller, Simon L Girard, Franziska Hopfner, et al.Nature Communications|October 31, 2019
Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3Rahel T Florian, Florian Kraft, Elsa Leitão, et al.Pageof 10