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A E Harding

Showing results (221-230 of 241) with videos related to

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Nature Genetics|December 1, 1992
Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophyA R La Spada, D B Roling, A E Harding, et al.
Journal of the Neurological Sciences|January 1, 1992
Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathyS R Hammans, M G Sweeney, I J Holt, et al.
Brain : a Journal of Neurology|June 1, 1993
The mitochondrial DNA transfer RNA(Lys)A-->G(8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF). Relationship of clinical phenotype to proportion of mutant mitochondrial DNAS R Hammans, M G Sweeney, M Brockington, et al.
Acta Neuropathologica|January 1, 1993
The sensory neuropathy of Friedreich's ataxia: an autopsy study of a case with prolonged survivalS Jitpimolmard, J Small, R H King, et al.
Brain : a Journal of Neurology|July 29, 1998
The relationship between striatal dopamine receptor binding and cognitive performance in Huntington's diseaseA D Lawrence, R A Weeks, D J Brooks, et al.
Biochimica Et Biophysica Acta|May 24, 1995
Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotypeJ A Morgan-Hughes, M G Sweeney, J M Cooper, et al.
Neurology|March 1, 1995
Acanthocytosis, retinitis pigmentosa, and pallidal degeneration: a report of three patients, including the second reported case with hypoprebetalipoproteinemia (HARP syndrome)R W Orrell, P J Amrolia, A Heald, et al.
Annals of Neurology|March 1, 1994
Nigrostriatal function in vitamin E deficiency: clinical, experimental, and positron emission tomographic studiesD T Dexter, D J Brooks, A E Harding, et al.
Brain : a Journal of Neurology|August 1, 1995
Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathyM M Reilly, D Adams, D R Booth, et al.
Molecular and Cellular Probes|December 1, 1994
Apo E genotypes in multiple sclerosis, Parkinson's disease, schwannomas and late-onset Alzheimer's diseaseD C Rubinsztein, C S Hanlon, R M Irving, et al.
Pageof 25

Showing results (221-230 of 241) with videos related to

Sort By:
Pageof 25
Nature Genetics|December 1, 1992
Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophyA R La Spada, D B Roling, A E Harding, et al.
Journal of the Neurological Sciences|January 1, 1992
Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathyS R Hammans, M G Sweeney, I J Holt, et al.
Brain : a Journal of Neurology|June 1, 1993
The mitochondrial DNA transfer RNA(Lys)A-->G(8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF). Relationship of clinical phenotype to proportion of mutant mitochondrial DNAS R Hammans, M G Sweeney, M Brockington, et al.
Acta Neuropathologica|January 1, 1993
The sensory neuropathy of Friedreich's ataxia: an autopsy study of a case with prolonged survivalS Jitpimolmard, J Small, R H King, et al.
Brain : a Journal of Neurology|July 29, 1998
The relationship between striatal dopamine receptor binding and cognitive performance in Huntington's diseaseA D Lawrence, R A Weeks, D J Brooks, et al.
Biochimica Et Biophysica Acta|May 24, 1995
Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotypeJ A Morgan-Hughes, M G Sweeney, J M Cooper, et al.
Neurology|March 1, 1995
Acanthocytosis, retinitis pigmentosa, and pallidal degeneration: a report of three patients, including the second reported case with hypoprebetalipoproteinemia (HARP syndrome)R W Orrell, P J Amrolia, A Heald, et al.
Annals of Neurology|March 1, 1994
Nigrostriatal function in vitamin E deficiency: clinical, experimental, and positron emission tomographic studiesD T Dexter, D J Brooks, A E Harding, et al.
Brain : a Journal of Neurology|August 1, 1995
Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathyM M Reilly, D Adams, D R Booth, et al.
Molecular and Cellular Probes|December 1, 1994
Apo E genotypes in multiple sclerosis, Parkinson's disease, schwannomas and late-onset Alzheimer's diseaseD C Rubinsztein, C S Hanlon, R M Irving, et al.
Pageof 25