Cytochrome c Oxidase Deficiency Associated with the First Stop-Codon Point Mutation in Human mtDNA
Hanna, M.G., Nelson, I.P., Rahman, S., Lane, R.J.M., Land, J., Heales, S., Cooper, M.J., Schapira, A.H.V., Morgan-Hughes, J.A., Wood, N.W.
Published in American journal of human genetics (01.07.1998)
Published in American journal of human genetics (01.07.1998)
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Journal Article
New phenotypic diversity associated with the mitochondrial tRNASer(UCN) gene mutation
Pulkes, T., Liolitsa, D., Eunson, L.H., Rose, M., Nelson, I.P., Rahman, S., Poulton, J., Marchington, D.R., Landon, D.N., Debono, A.G., Morgan-Hughes, J.A., Hanna, M.G.
Published in Neuromuscular disorders : NMD (01.05.2005)
Published in Neuromuscular disorders : NMD (01.05.2005)
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Journal Article
New phenotypic diversity associated with the mitochondrial tRNA Ser(UCN) gene mutation
Pulkes, T., Liolitsa, D., Eunson, L.H., Rose, M., Nelson, I.P., Rahman, S., Poulton, J., Marchington, D.R., Landon, D.N., Debono, A.G., Morgan-Hughes, J.A., Hanna, M.G.
Published in Neuromuscular disorders : NMD (2005)
Published in Neuromuscular disorders : NMD (2005)
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Journal Article
Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples
Hammans, S.R., Sweeney, M.G., Brockington, M., Morgan-Hughes, J.A., Harding, A.E.
Published in The Lancet (British edition) (01.06.1991)
Published in The Lancet (British edition) (01.06.1991)
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Journal Article
Mitochondrial encephalopathy with multiple mitochondrial DNA deletions: a report of two families and two sporadic cases with unusual clinical and neuropathological features
Chalmers, R.M, Brockington, M, Howard, R.S, Lecky, B.R.F, Morgan-Hughes, J.A, Harding, A.E
Published in Journal of the neurological sciences (01.11.1996)
Published in Journal of the neurological sciences (01.11.1996)
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Journal Article
Kearns-Sayre syndrome associated with mitochondrial DNA deletion or duplication: a molecular genetic and pathological study
Brockington, M., Alsanjari, N., Sweeney, M.G., Morgan-Hughes, J.A., Scaravilli, F., Harding, A.E.
Published in Journal of the neurological sciences (01.07.1995)
Published in Journal of the neurological sciences (01.07.1995)
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Journal Article
Erratum to “Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A → G (MERRF) mutation: relationship to proportion of mutant mitochondrial DNA”
Hanna, M.G., Nelson, I.P., Morgan-Hughes, J.A., Harding, A.E.
Published in Journal of the neurological sciences (01.09.1995)
Published in Journal of the neurological sciences (01.09.1995)
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Journal Article
Erratum to “Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A → G (MERRF) mutation: relationship to proportion of mutant mitochondrial DNA”: J. Neurol. Sci. 130 (1995) 154–160
Hanna, M.G., Nelson, I.P., Morgan-Hughes, J.A., Harding, A.E.
Published in Journal of the neurological sciences (1995)
Published in Journal of the neurological sciences (1995)
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Journal Article
Fifty year follow-up of a patient with central core disease shows slow but definite progression
Lamont, P.J, Dubowitz, V, Landon, D.N, Davis, M, Morgan-Hughes, J.A
Published in Neuromuscular disorders : NMD (01.08.1998)
Published in Neuromuscular disorders : NMD (01.08.1998)
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Journal Article
Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A → G (MERRF) mutation: relationship to proportion of mutant mitochondrial DNA
Hanna, M.G., Nelson, I.P., Morgan-Hughes, J.A., Harding, A.E.
Published in Journal of the neurological sciences (01.06.1995)
Published in Journal of the neurological sciences (01.06.1995)
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Journal Article
Mitochondrial DNA mutation underlying Leigh's syndrome: Clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsy
Sweeney, M.G., Hammans, S.R., Duchen, L.W., Cooper, J.M., Schapira, A.H.V., Kennedy, C.R., Jacobs, J.M., Youl, B.D., Morgan-Hughes, J.A., Harding, A.E.
Published in Journal of the neurological sciences (1994)
Published in Journal of the neurological sciences (1994)
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Journal Article
Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathy
Hammans, S.R., Sweeney, M.G., Holt, I.J., Cooper, J.M., Toscano, A., Clark, J.B., Morgan-Hughes, J.A., Harding, A.E.
Published in Journal of the neurological sciences (1992)
Published in Journal of the neurological sciences (1992)
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Journal Article
Myoadenylate deaminase deficiency or not?
Hayes, D.J., Summers, Beatrice A., Morgan-Hughes, J.A.
Published in Journal of the neurological sciences (01.01.1982)
Published in Journal of the neurological sciences (01.01.1982)
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Journal Article
Histotopochemie und histopathochemie des peripheren nervensystems bei verletzungen und tumoren: (Histotopochemistry and histopathochemistry of the peripheral nervous system with lesions and tumours), by E. Thomas, 85 pages, 44 illustrations, Gustav Fischer, Stuttgart, 1969, DM 28.
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