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Movement Disorders : Official Journal of the Movement Disorder Society|August 22, 2014
DYT16 revisited: exome sequencing identifies PRKRA mutations in a European dystonia familyMichael Zech, Florian Castrop, Barbara Schormair, et al.Cardiovascular Research|January 19, 2010
IRAG determines nitric oxide- and atrial natriuretic peptide-mediated smooth muscle relaxationMatthias Desch, Katja Sigl, Bernhard Hieke, et al.American Journal of Human Genetics|May 26, 2015
Recessive mutations in the α3 (VI) collagen gene COL6A3 cause early-onset isolated dystoniaMichael Zech, Daniel D Lam, Ludmila Francescatto, et al.Neurogenetics|August 30, 2017
Molecular diversity of combined and complex dystonia: insights from diagnostic exome sequencingMichael Zech, Robert Jech, Matias Wagner, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 27, 2016
Clinical exome sequencing in early-onset generalized dystonia and large-scale resequencing follow-upMichael Zech, Sylvia Boesch, Angela Jochim, et al.Plos One|January 4, 2014
Niemann-Pick C disease gene mutations and age-related neurodegenerative disordersMichael Zech, Georg Nübling, Florian Castrop, et al.Der Nervenarzt|March 14, 2024
[How the implementation of a school for people with Parkinson's disease can succeed-Results of a consensus study and a formative evaluation]Tanita Gerschel, Scally Prokop, Lara Schulze, et al.The Lancet. Neurology|October 25, 2020
Monogenic variants in dystonia: an exome-wide sequencing studyMichael Zech, Robert Jech, Sylvia Boesch, et al.Nature Genetics|October 1, 2013
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis, Ashley H Beecham, Nikolaos A Patsopoulos, et al.Pageof 3