Showing results (301-310 of 389) with videos related to
Sort By:
Pageof 39
Brain Research. Molecular Brain Research|February 25, 2000
Upregulation of cytosolic branched chain aminotransferase in substantia nigra following developmental striatal target injuryN G Kholodilov, M Neystat, T F Oo, et al.Neurology|September 1, 1994
Metabolic topography of the hemiparkinsonism-hemiatrophy syndromeS Przedborski, N Giladi, S Takikawa, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1995
Adult onset idiopathic torsion dystonia is excluded from the DYT 1 region (9q34) in a Swedish familyG Holmgren, L Ozelius, L Forsgren, et al.Journal of Neuroscience Methods|March 1, 1982
2-deoxyglucose autoradiography of single motor units: labeling of individual acutely active muscle fibersJ Toop, R E Burke, R P Dum, et al.Neurology|April 12, 2012
Network correlates of disease severity in multiple system atrophyK L Poston, C C Tang, T Eckert, et al.Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1993
Neuropathology of lubag (x-linked dystonia parkinsonism)C H Waters, P L Faust, J Powers, et al.Brain Research|June 7, 1991
Sham transplantation protects against 6-hydroxydopamine-induced dopaminergic toxicity in rats: behavioral and morphological evidenceS Przedborski, M Levivier, V Kostic, et al.Nature Genetics|February 1, 1995
Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder populationN Risch, D de Leon, L Ozelius, et al.Brain Research|December 11, 1989
Regional effects of 6-hydroxydopamine (6-OHDA) on free radical scavengers in rat brainA S Perumal, W K Tordzro, M Katz, et al.Neurology|December 11, 2002
Diagnostic criteria for dystonia in DYT1 familiesS B Bressman, D Raymond, K Wendt, et al.Pageof 39