Showing results (291-300 of 314) with videos related to
Sort By:
Pageof 32
Movement Disorders : Official Journal of the Movement Disorder Society|November 1, 1994
Exclusion of the DYT1 locus in a non-Jewish family with early-onset dystoniaS B Bressman, A L Hunt, G A Heiman, 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.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 1, 2022
Exome sequencing as first-tier test for fetuses with severe central nervous system structural anomaliesY Yaron, V Ofen Glassner, A Mory, 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.Genomics|January 25, 2000
The TOR1A (DYT1) gene family and its role in early onset torsion dystoniaL J Ozelius, C E Page, C Klein, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|February 8, 2011
High prevalence of malignant melanoma in Israeli patients with Parkinson's diseaseR Inzelberg, J M Rabey, E Melamed, et al.Annals of Neurology|October 1, 1996
Exclusion of the DYT1 locus in familial torticollisS B Bressman, T T Warner, L Almasy, et al.Pageof 32