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Neurology|August 19, 2007
Sixty hertz pallidal deep brain stimulation for primary torsion dystoniaR L Alterman, J Miravite, D Weisz, et al.
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.
Neurology|January 1, 1985
Validity and reliability of a rating scale for the primary torsion dystoniasR E Burke, S Fahn, C D Marsden, et al.
Annals of Neurology|November 18, 2000
A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathyD Thyagarajan, S Bressman, C Bruno, et al.
Neuroscience Letters|December 14, 2011
Gender differences in the IL6 -174G>C and ESR2 1730G>A polymorphisms and the risk of Parkinson's diseaseM San Luciano, L Ozelius, R B Lipton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 1, 1995
Speech dysfunction in early Parkinson's diseaseC Stewart, L Winfield, A Hunt, et al.
Integrative Organismal Biology (Oxford, England)|April 1, 2021
Emersion and Terrestrial Locomotion of the Northern Snakehead (<i>Channa argus</i>) on Multiple SubstratesN R Bressman, J W Love, T W King, 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.
The Lancet. Neurology|April 7, 2009
Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening studySusan B Bressman, Deborah Raymond, Tania Fuchs, et al.
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