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A E Harding

Showing results (181-190 of 241) with videos related to

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Brain : a Journal of Neurology|August 1, 1994
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxiasP Giunti, M G Sweeney, M Spadaro, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1990
Movement disorders in mitochondrial myopathies. A study of nine cases with two autopsy studiesD D Truong, A E Harding, F Scaravilli, et al.
Neurology|June 1, 1997
Evaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease: evidence for association of a DRD2 alleleV Planté-Bordeneuve, D Taussig, F Thomas, et al.
Journal of the Neurological Sciences|November 1, 1996
Mitochondrial encephalopathy with multiple mitochondrial DNA deletions: a report of two families and two sporadic cases with unusual clinical and neuropathological featuresR M Chalmers, M Brockington, R S Howard, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 1, 1985
The retinal manifestations of mitochondrial myopathy. A study of 22 casesM A Mullie, A E Harding, R K Petty, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1997
Cerebellar presentation of multiple system atrophyG K Wenning, E Kraft, R Beck, et al.
Biochemical Society Transactions|August 1, 1990
Mitochondrial myopathies: clinical defectsJ A Morgan-Hughes, J M Cooper, I J Holt, et al.
Lancet (London, England)|July 1, 1989
Diagnosis of Gerstmann-Sträussler syndrome in familial dementia with prion protein gene analysisJ Collinge, A E Harding, F Owen, et al.
Journal of Medical Genetics|November 1, 1987
Variant forms of ataxia telangiectasiaA M Taylor, E Flude, B Laher, et al.
Biochimica Et Biophysica Acta|July 25, 1990
The molecular pathology of respiratory-chain dysfunction in human mitochondrial myopathiesJ A Morgan-Hughes, A H Schapira, J M Cooper, et al.
Pageof 25

Showing results (181-190 of 241) with videos related to

Sort By:
Pageof 25
Brain : a Journal of Neurology|August 1, 1994
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxiasP Giunti, M G Sweeney, M Spadaro, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1990
Movement disorders in mitochondrial myopathies. A study of nine cases with two autopsy studiesD D Truong, A E Harding, F Scaravilli, et al.
Neurology|June 1, 1997
Evaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease: evidence for association of a DRD2 alleleV Planté-Bordeneuve, D Taussig, F Thomas, et al.
Journal of the Neurological Sciences|November 1, 1996
Mitochondrial encephalopathy with multiple mitochondrial DNA deletions: a report of two families and two sporadic cases with unusual clinical and neuropathological featuresR M Chalmers, M Brockington, R S Howard, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 1, 1985
The retinal manifestations of mitochondrial myopathy. A study of 22 casesM A Mullie, A E Harding, R K Petty, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1997
Cerebellar presentation of multiple system atrophyG K Wenning, E Kraft, R Beck, et al.
Biochemical Society Transactions|August 1, 1990
Mitochondrial myopathies: clinical defectsJ A Morgan-Hughes, J M Cooper, I J Holt, et al.
Lancet (London, England)|July 1, 1989
Diagnosis of Gerstmann-Sträussler syndrome in familial dementia with prion protein gene analysisJ Collinge, A E Harding, F Owen, et al.
Journal of Medical Genetics|November 1, 1987
Variant forms of ataxia telangiectasiaA M Taylor, E Flude, B Laher, et al.
Biochimica Et Biophysica Acta|July 25, 1990
The molecular pathology of respiratory-chain dysfunction in human mitochondrial myopathiesJ A Morgan-Hughes, A H Schapira, J M Cooper, et al.
Pageof 25