Showing results (81-90 of 95) with videos related to
Sort By:
Pageof 10
Nature Communications|November 13, 2024
Genome-wide meta-analysis of myasthenia gravis uncovers new loci and provides insights into polygenic predictionAlice Braun, Sudhanshu Shekhar, Daniel F Levey, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 11, 2025
Rare but Relevant? Assessing Variants in Dystonia-Linked Genes in Parkinson's DiseaseLara M Lange, Zih-Hua Fang, Laurel Screven, et al.American Journal of Human Genetics|November 12, 2013
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndromeArvid Suls, Johanna A Jaehn, Angela Kecskés, et al.Nature Genetics|July 15, 2009
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic strokeDaniel F Gudbjartsson, Hilma Holm, Solveig Gretarsdottir, et al.Brain : a Journal of Neurology|March 8, 2022
Clinical, serological and genetic predictors of response to immunotherapy in anti-IgLON5 diseaseThomas Grüter, Franziska E Möllers, Anja Tietz, 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.Brain : a Journal of Neurology|March 29, 2022
A genome-wide association study in autoimmune neurological syndromes with anti-GAD65 autoantibodiesChristine Strippel, Marisol Herrera-Rivero, Mareike Wendorff, et al.BMC Geriatrics|February 8, 2020
Motor, cognitive and mobility deficits in 1000 geriatric patients: protocol of a quantitative observational study before and after routine clinical geriatric treatment - the ComOn-studyJohanna Geritz, Sara Maetzold, Maren Steffen, et al.Nature Genetics|November 25, 2014
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissectionStéphanie Debette, Yoichiro Kamatani, Tiina M Metso, et al.Movement Disorders : Official Journal of the Movement Disorder Society|August 23, 2022
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System AtrophyFranziska Hopfner, Anja K Tietz, Viktoria C Ruf, et al.Pageof 10