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Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2013
Genetics of dystonia: what's known? What's new? What's next?Katja Lohmann, Christine Klein
Current Neurology and Neuroscience Reports|March 12, 2017
Update on the Genetics of DystoniaKatja Lohmann, Christine Klein
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|July 24, 2014
Next generation sequencing and the future of genetic diagnosisKatja Lohmann, Christine Klein
Current Opinion in Neurology|July 11, 2007
Impact of recent genetic findings in Parkinson's diseaseChristine Klein, Katja Lohmann-Hedrich
Current Opinion in Neurology|July 10, 2012
Genetics of Parkinson disease and other movement disordersKishore R Kumar, Katja Lohmann, Christine Klein
Neurology|March 29, 2012
Fixing the broken system of genetic locus symbols: Parkinson disease and dystonia as examplesConnie Marras, Katja Lohmann, Anthony Lang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 30, 2011
Whispering dysphonia in an Australian family (DYT4): a clinical and genetic reappraisalRobert A Wilcox, Susen Winkler, Katja Lohmann, et al.
Neurobiology of Aging|January 15, 2014
Mutations in VPS26A are not a frequent cause of Parkinson's diseaseEva Koschmidder, Brit Mollenhauer, Meike Kasten, et al.
Parkinsonism & Related Disorders|July 1, 2019
The sooner, the later - Delayed diagnosis in Parkinson's disease due to Parkin mutationsMax Borsche, Alexander Balck, Meike Kasten, et al.
Parkinsonism & Related Disorders|April 5, 2021
Involuntary moaning in a Hispanic family with eight affected membersMaria Gisatulin, Malco Rossi, Claudia Perandones, et al.
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