Showing results (11-20 of 81) with videos related to

Sort By:
Pageof 9
Brain : a Journal of Neurology|April 26, 2011
Impaired sequence learning in dystonia mutation carriers: a genotypic effectMaren Carbon, Miklos Argyelan, Maria Felice Ghilardi, et al.
Parkinsonism & Related Disorders|September 1, 2015
The emerging role of SMPD1 mutations in Parkinson's disease: Implications for future studiesZiv Gan-Or, Avi Orr-Urtreger, Roy N Alcalay, et al.
Annals of Neurology|August 5, 2004
Microstructural white matter changes in carriers of the DYT1 gene mutationMaren Carbon, Peter B Kingsley, Sherwin Su, et al.
Annals of Clinical and Translational Neurology|November 22, 2017
Sex differences in LRRK2 G2019S and idiopathic Parkinson's DiseaseMarta San Luciano, Cuiling Wang, Roberto A Ortega, et al.
Neurology|August 24, 2012
Lower cognitive performance in healthy G2019S LRRK2 mutation carriersAvner Thaler, Anat Mirelman, Tanya Gurevich, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 26, 2011
Mood and cognition in leucine-rich repeat kinase 2 G2019S Parkinson's diseaseVicki Shanker, Mark Groves, Gary Heiman, et al.
Biometrika|September 29, 2015
Efficient Estimation of Nonparametric Genetic Risk Function with Censored DataYuanjia Wang, Baosheng Liang, Xingwei Tong, et al.
Neurology|January 4, 2013
Metabolic changes in DYT11 myoclonus-dystoniaMaren Carbon, Deborah Raymond, Laurie Ozelius, et al.
Annals of Neurology|July 3, 2003
Impaired sequence learning in carriers of the DYT1 dystonia mutationMaria-Felice Ghilardi, Maren Carbon, Giulia Silvestri, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 22, 2011
Inclusion and exclusion criteria for DBS in dystoniaHelen Bronte-Stewart, Takaomi Taira, Francesc Valldeoriola, et al.
Pageof 9