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A E Harding

Showing results (161-170 of 241) with videos related to

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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.
Genomics|January 1, 1993
Evidence for locus heterogeneity in autosomal dominant torsion dystoniaF Ahmad, M B Davis, H M Waddy, et al.
Neurology|October 1, 1993
Genomic imprinting and anticipation in idiopathic torsion dystoniaM C LaBuda, N A Fletcher, A D Korczyn, et al.
Archives of Disease in Childhood|October 15, 1998
Clinical and laboratory findings in referrals for mitochondrial DNA analysisP J Lamont, R Surtees, C E Woodward, et al.
Pageof 25

Showing results (161-170 of 241) with videos related to

Sort By:
Pageof 25
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.
Genomics|January 1, 1993
Evidence for locus heterogeneity in autosomal dominant torsion dystoniaF Ahmad, M B Davis, H M Waddy, et al.
Neurology|October 1, 1993
Genomic imprinting and anticipation in idiopathic torsion dystoniaM C LaBuda, N A Fletcher, A D Korczyn, et al.
Archives of Disease in Childhood|October 15, 1998
Clinical and laboratory findings in referrals for mitochondrial DNA analysisP J Lamont, R Surtees, C E Woodward, et al.
Pageof 25