Showing results (361-370 of 389) with videos related to
Sort By:
Pageof 39
Neurology|June 1, 1997
Secondary dystonia and the DYTI geneS B Bressman, D de Leon, D Raymond, et al.Neurology|May 10, 2000
The DYT1 phenotype and guidelines for diagnostic testingS B Bressman, C Sabatti, D Raymond, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1988
Neurochemical findings in neuroacanthocytosisJ G de Yebenes, M F Brin, M A Mena, et al.The New England Journal of Medicine|March 10, 2001
Transplantation of embryonic dopamine neurons for severe Parkinson's diseaseC R Freed, P E Greene, R E Breeze, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 18, 2004
Subthalamic nucleus stimulation in advanced Parkinson's disease: blinded assessments at one year follow upB Ford, L Winfield, S L Pullman, et al.Molecular Genetics & Genomic Medicine|September 28, 2013
Increased Rate of Sporadic and Recurrent Rare Genic Copy Number Variants in Parkinson's Disease Among Ashkenazi JewsX Liu, R Cheng, X Ye, et al.Annals of Neurology|February 1, 1990
Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34P L Kramer, D de Leon, L Ozelius, et al.American Journal of Human Genetics|September 1, 1994
The DYT1 gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-JewsP L Kramer, G A Heiman, T Gasser, et al.Neurology|September 19, 2007
Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson diseaseL N Clark, B M Ross, Y Wang, et al.Neurology|October 20, 2006
Frequency of LRRK2 mutations in early- and late-onset Parkinson diseaseL N Clark, Y Wang, E Karlins, et al.Pageof 39