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Parkinsonism & Related Disorders|April 27, 2017
Topography of essential tremorWei Chen, Franziska Hopfner, Silke Szymczak, et al.
Neurogenetics|March 29, 2021
Evidence for pathogenicity of variant ATM Val1729Leu in a family with ataxia telangiectasiaAli S Shalash, Thomas W Rösler, Mohamed Salama, et al.
Brain Research|May 17, 2017
Gut microbiota in Parkinson disease in a northern German cohortFranziska Hopfner, Axel Künstner, Stefanie H Müller, et al.
Heliyon|July 21, 2021
Atypical pantothenate kinase-associated neurodegeneration with variable phenotypes in an Egyptian familyAli S Shalash, Thomas W Rösler, Ibrahim Y Abdelrahman, et al.
Neurology. Genetics|November 18, 2017
c.207C>G mutation in sepiapterin reductase causes autosomal dominant dopa-responsive dystoniaAli S Shalash, Thomas W Rösler, Stefanie H Müller, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 30, 2015
The impact of rare variants in FUS in essential tremorFranziska Hopfner, Giovanni Stevanin, Stefanie H Müller, et al.
Plos Genetics|September 21, 2020
Candidate variants in TUB are associated with familial tremorM Reza Sailani, Fereshteh Jahanbani, Charles W Abbott, et al.
Translational Neurodegeneration|April 16, 2019
No association between Parkinson disease and autoantibodies against NMDA-type glutamate receptorsFranziska Hopfner, Stefanie H Müller, Dagmar Steppat, 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.
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