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A E Harding

Showing results (151-160 of 241) with videos related to

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Journal of the Neurological Sciences|November 1, 1994
HLA class II genotypes in Leber's hereditary optic neuropathyG G Govan, P R Smith, H Kellar-Wood, et al.
Lancet (London, England)|June 1, 1991
Mitochondrial encephalopathies: molecular genetic diagnosis from blood samplesS R Hammans, M G Sweeney, M Brockington, et al.
Brain : a Journal of Neurology|October 6, 1997
Cortical control of movement in Huntington's disease. A PET activation studyR A Weeks, A Ceballos-Baumann, P Piccini, et al.
Human Molecular Genetics|March 1, 1996
Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneityO Bandmann, T G Nygaard, R Surtees, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1988
Leukocyte glutamate dehydrogenase activity in patients with degenerative neurological disordersD Aubby, H K Saggu, P Jenner, et al.
Annals of Neurology|March 1, 1995
A new mitochondrial DNA mutation associated with progressive dementia and chorea: a clinical, pathological, and molecular genetic studyI Nelson, M G Hanna, N Alsanjari, et al.
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.
The New England Journal of Medicine|July 4, 1985
Spinocerebellar degeneration associated with a selective defect of vitamin E absorptionA E Harding, S Matthews, S Jones, et al.
Pageof 25

Showing results (151-160 of 241) with videos related to

Sort By:
Pageof 25
Journal of the Neurological Sciences|November 1, 1994
HLA class II genotypes in Leber's hereditary optic neuropathyG G Govan, P R Smith, H Kellar-Wood, et al.
Lancet (London, England)|June 1, 1991
Mitochondrial encephalopathies: molecular genetic diagnosis from blood samplesS R Hammans, M G Sweeney, M Brockington, et al.
Brain : a Journal of Neurology|October 6, 1997
Cortical control of movement in Huntington's disease. A PET activation studyR A Weeks, A Ceballos-Baumann, P Piccini, et al.
Human Molecular Genetics|March 1, 1996
Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneityO Bandmann, T G Nygaard, R Surtees, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1988
Leukocyte glutamate dehydrogenase activity in patients with degenerative neurological disordersD Aubby, H K Saggu, P Jenner, et al.
Annals of Neurology|March 1, 1995
A new mitochondrial DNA mutation associated with progressive dementia and chorea: a clinical, pathological, and molecular genetic studyI Nelson, M G Hanna, N Alsanjari, et al.
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.
The New England Journal of Medicine|July 4, 1985
Spinocerebellar degeneration associated with a selective defect of vitamin E absorptionA E Harding, S Matthews, S Jones, et al.
Pageof 25