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American Journal of Human Genetics|March 1, 1992
Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi JewsL J Ozelius, P L Kramer, D de Leon, et al.Neurology|February 14, 2007
Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCE mutation carriersC W Hess, D Raymond, P de Carvalho Aguiar, et al.Annals of Neurology|August 12, 1999
Rapid-onset dystonia-parkinsonism: linkage to chromosome 19q13P L Kramer, M Mineta, C Klein, et al.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.Neurology|December 26, 2014
Reorganization of corticostriatal circuits in healthy G2019S LRRK2 carriersRick C Helmich, Avner Thaler, Bart F L van Nuenen, et al.Journal of Clinical Medicine|June 2, 2021
Short-Stay Hospitalizations for Patients with COVID-19: A Retrospective Cohort StudyAustin S Kilaru, Kathleen Lee, Lindsay Grossman, et al.Journal of Parkinson'S Disease|November 8, 2021
Sex-Related Longitudinal Change of Motor, Non-Motor, and Biological Features in Early Parkinson's DiseaseMarina Picillo, David-Erick LaFontant, Susan Bressman, et al.Neurology|February 1, 1994
A study of idiopathic torsion dystonia in a non-Jewish family: evidence for genetic heterogeneityS B Bressman, G A Heiman, T G Nygaard, et al.Parkinsonism & Related Disorders|December 2, 2014
Neuropsychological performance in LRRK2 G2019S carriers with Parkinson's diseaseRoy N Alcalay, Helen Mejia-Santana, Anat Mirelman, et al.Neurology|October 23, 2002
Clinical findings of a myoclonus-dystonia family with two distinct mutationsD Doheny, F Danisi, C Smith, et al.Pageof 30