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Journal of the Neurological Sciences|July 1, 1995
Kearns-Sayre syndrome associated with mitochondrial DNA deletion or duplication: a molecular genetic and pathological studyM Brockington, N Alsanjari, M G Sweeney, et al.Brain Research. Molecular Brain Research|March 1, 1992
A dementing illness associated with a novel insertion in the prion protein geneF Owen, M Poulter, J Collinge, et al.The Quarterly Journal of Medicine|November 1, 1993
Mitochondrial myopathy associated with sudden death in young adults and a novel mutation in the mitochondrial DNA leucine transfer RNA(UUR) geneM G Sweeney, S Bundey, M Brockington, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 1994
The neuropathological features of neuroacanthocytosisJ O Rinne, S E Daniel, F Scaravilli, et al.Brain : a Journal of Neurology|April 1, 1992
A molecular genetic study of focal histochemical defects in mitochondrial encephalomyopathiesS R Hammans, M G Sweeney, D A Wicks, et al.Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|October 6, 1997
11C-diprenorphine binding in Huntington's disease: a comparison of region of interest analysis with statistical parametric mappingR A Weeks, V J Cunningham, P Piccini, et al.Nature|July 4, 1991
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophyA R La Spada, E M Wilson, D B Lubahn, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 1995
CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophyV Planté-Bordeneuve, O Bandmann, G Wenning, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1990
Mitochondrial DNA analysis in Parkinson's diseaseA H Schapira, I J Holt, M Sweeney, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1988
Central motor conduction in degenerative ataxic disorders: a magnetic stimulation studyD Claus, A E Harding, C W Hess, et al.Pageof 21