Schapira AH - Search Results

1

Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.

Hanna MG, Nelson IP, Rahman S, Lane RJ, Land J, Heales S, Cooper MJ, Schapira AH, Morgan-Hughes JA, Wood NW. Hanna MG, et al. Among authors: schapira ah. Am J Hum Genet. 1998 Jul;63(1):29-36. doi: 10.1086/301910. Am J Hum Genet. 1998. PMID: 9634511 Free PMC article.

2

One-step immunoaffinity purification of complex I subunits from beef heart mitochondria.

Haines AM, Cooper JM, Morgan-Hughes JA, Clark JB, Schapira AH. Haines AM, et al. Among authors: schapira ah. Protein Expr Purif. 1992 Jun;3(3):223-7. doi: 10.1016/1046-5928(92)90018-r. Protein Expr Purif. 1992. PMID: 1392618

3

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

4

Mitochondrial myopathy with a defect of mitochondrial-protein transport.

Schapira AH, Cooper JM, Morgan-Hughes JA, Landon DN, Clark JB. Schapira AH, et al. N Engl J Med. 1990 Jul 5;323(1):37-42. doi: 10.1056/NEJM199007053230107. N Engl J Med. 1990. PMID: 2113185 Free article. No abstract available.

5

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. Among authors: schapira ah. 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

6

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. Among authors: schapira ah. Biochem Soc Trans. 1990 Aug;18(4):517-9. doi: 10.1042/bst0180517. Biochem Soc Trans. 1990. PMID: 2177405 No abstract available.

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: schapira ah. 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: schapira ah. Biochem Soc Trans. 1990 Aug;18(4):523-6. doi: 10.1042/bst0180523. Biochem Soc Trans. 1990. PMID: 2276423 No abstract available.

9

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

10

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

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