Cooper JM - Search Results

1

Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutation.

Hanna MG, Nelson I, Sweeney MG, Cooper JM, Watkins PJ, Morgan-Hughes JA, Harding AE. Hanna MG, et al. Among authors: cooper jm. Am J Hum Genet. 1995 May;56(5):1026-33. Am J Hum Genet. 1995. PMID: 7726155 Free PMC article.

2

Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype.

Morgan-Hughes JA, Sweeney MG, Cooper JM, Hammans SR, Brockington M, Schapira AH, Harding AE, Clark JB. Morgan-Hughes JA, et al. Among authors: cooper jm. Biochim Biophys Acta. 1995 May 24;1271(1):135-40. doi: 10.1016/0925-4439(95)00020-5. Biochim Biophys Acta. 1995. PMID: 7599199 Free article.

3

A missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathy.

Rahman S, Taanman JW, Cooper JM, Nelson I, Hargreaves I, Meunier B, Hanna MG, García JJ, Capaldi RA, Lake BD, Leonard JV, Schapira AH. Rahman S, et al. Among authors: cooper jm. Am J Hum Genet. 1999 Oct;65(4):1030-9. doi: 10.1086/302590. Am J Hum Genet. 1999. PMID: 10486321 Free PMC article.

4

Mitochondrial DNA mutation underlying Leigh's syndrome: clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsy.

Sweeney MG, Hammans SR, Duchen LW, Cooper JM, Schapira AH, Kennedy CR, Jacobs JM, Youl BD, Morgan-Hughes JA, Harding AE. Sweeney MG, et al. Among authors: cooper jm. J Neurol Sci. 1994 Jan;121(1):57-65. doi: 10.1016/0022-510x(94)90157-0. J Neurol Sci. 1994. PMID: 8133313

5

Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathy.

Hammans SR, Sweeney MG, Holt IJ, Cooper JM, Toscano A, Clark JB, Morgan-Hughes JA, Harding AE. Hammans SR, et al. Among authors: cooper jm. J Neurol Sci. 1992 Jan;107(1):87-92. doi: 10.1016/0022-510x(92)90213-5. J Neurol Sci. 1992. PMID: 1315844

6

The molecular pathology of human respiratory chain defects.

Morgan-Hughes JA, Cooper JM, Schapira AH, Sweeny M, Holt IJ, Harding AE, Clark JB. Morgan-Hughes JA, et al. Among authors: cooper jm. Rev Neurol (Paris). 1991;147(6-7):450-4. Rev Neurol (Paris). 1991. PMID: 1962049 Review.

7

Mitochondrial myopathies: genetic defects.

Harding AE, Holt IJ, Cooper JM, Schapira AH, Sweeney M, Clark JB, Morgan-Hughes JA. Harding AE, et al. Among authors: cooper jm. Biochem Soc Trans. 1990 Aug;18(4):519-22. doi: 10.1042/bst0180519. Biochem Soc Trans. 1990. PMID: 2276422 Review. No abstract available.

8

Mitochondrial myopathies: clinical defects.

Morgan-Hughes JA, Cooper JM, Holt IJ, Harding AE, Schapira AH, Clark JB. Morgan-Hughes JA, et al. Among authors: cooper jm. Biochem Soc Trans. 1990 Aug;18(4):523-6. doi: 10.1042/bst0180523. Biochem Soc Trans. 1990. PMID: 2276423 No abstract available.

9

Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA.

Holt IJ, Harding AE, Cooper JM, Schapira AH, Toscano A, Clark JB, Morgan-Hughes JA. Holt IJ, et al. Among authors: cooper jm. Ann Neurol. 1989 Dec;26(6):699-708. doi: 10.1002/ana.410260603. Ann Neurol. 1989. PMID: 2604380

10

Molecular defects of NADH-ubiquinone oxidoreductase (complex I) in mitochondrial diseases.

Morgan-Hughes JA, Schapira AH, Cooper JM, Clark JB. Morgan-Hughes JA, et al. Among authors: cooper jm. J Bioenerg Biomembr. 1988 Jun;20(3):365-82. doi: 10.1007/BF00769638. J Bioenerg Biomembr. 1988. PMID: 3136150 Review.

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