Morgan-Hughes JA - Search Results

1

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. Rev Neurol (Paris). 1991;147(6-7):450-4. Rev Neurol (Paris). 1991. PMID: 1962049 Review.

2

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. J Neurol Sci. 1992 Jan;107(1):87-92. doi: 10.1016/0022-510x(92)90213-5. J Neurol Sci. 1992. PMID: 1315844

3

A molecular genetic study of focal histochemical defects in mitochondrial encephalomyopathies.

Hammans SR, Sweeney MG, Wicks DA, Morgan-Hughes JA, Harding AE. Hammans SR, et al. Brain. 1992 Apr;115 ( Pt 2):343-65. doi: 10.1093/brain/115.2.343. Brain. 1992. PMID: 1606473

4

The molecular pathology of respiratory-chain dysfunction in human mitochondrial myopathies.

Morgan-Hughes JA, Schapira AH, Cooper JM, Holt IJ, Harding AE, Clark JB. Morgan-Hughes JA, et al. Biochim Biophys Acta. 1990 Jul 25;1018(2-3):217-22. doi: 10.1016/0005-2728(90)90252-y. Biochim Biophys Acta. 1990. PMID: 2168209

5

Biochemical and molecular aspects of human mitochondrial respiratory chain disorders.

Cooper JM, Schapira AH, Holt IJ, Toscano A, Harding AE, Morgan-Hughes JA, Clark JB. Cooper JM, et al. Biochem Soc Trans. 1990 Aug;18(4):517-9. doi: 10.1042/bst0180517. Biochem Soc Trans. 1990. PMID: 2177405 No abstract available.

6

Mitochondrial myopathies: genetic defects.

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

7

Mitochondrial myopathies: clinical defects.

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

8

A mitochondrial encephalomyopathy with specific deficiencies of two respiratory chain polypeptides and a circulating autoantibody to a mitochondrial matrix protein.

Schapira AH, Cooper JM, Manneschi L, Vital C, Morgan-Hughes JA, Clark JB. Schapira AH, et al. Brain. 1990 Apr;113 ( Pt 2):419-32. doi: 10.1093/brain/113.2.419. Brain. 1990. PMID: 2328411

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. Ann Neurol. 1989 Dec;26(6):699-708. doi: 10.1002/ana.410260603. Ann Neurol. 1989. PMID: 2604380

10

Deletions of muscle mitochondrial DNA in mitochondrial myopathies: sequence analysis and possible mechanisms.

Holt IJ, Harding AE, Morgan-Hughes JA. Holt IJ, et al. Nucleic Acids Res. 1989 Jun 26;17(12):4465-9. doi: 10.1093/nar/17.12.4465. Nucleic Acids Res. 1989. PMID: 2748329 Free PMC article.

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