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European Journal of Human Genetics : EJHG|December 19, 2008
Dopamine receptor D3 gene and essential tremor in large series of German, Danish and French patientsDelia Lorenz, Stephan Klebe, Giovanni Stevanin, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 15, 2010
LINGO1 is not associated with Parkinson's disease in German patientsStephan Klebe, Sandra Thier, Delia Lorenz, et al.
Annals of Clinical and Translational Neurology|December 2, 2020
TDP-43 as structure-based biomarker in amyotrophic lateral sclerosisLéon Beyer, René Günther, Jan Christoph Koch, et al.
International Journal of Cardiology|May 26, 2015
The cardiomyopathy in Friedreich's ataxia - New biomarker for staging cardiac involvementFrank Weidemann, Dan Liu, Kai Hu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 27, 2015
High nigral iron deposition in LRRK2 and Parkin mutation carriers using R2* relaxometryNadya Pyatigorskaya, Michael Sharman, Jean-Christophe Corvol, et al.
Neurogenetics|October 16, 2008
Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegiaRebecca Schüle, Elisabeth Brandt, Kathrin N Karle, et al.
Pharmacoeconomics|March 19, 2021
Resource Utilization of Patients with Parkinson's Disease in the Late Stages of the Disease in Germany: Data from the CLaSP StudyChristopher Kruse, Sabrina Kretschmer, Anna Lipinski, et al.
Human Genetics|February 3, 2007
A novel locus for autosomal recessive spastic ataxia on chromosome 17pNaima Bouslam, Ahmed Bouhouche, Ali Benomar, et al.
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