Holt IJ - Search Results

1

Mitochondrial DNA polymorphism in mitochondrial myopathy.

Holt IJ, Harding AE, Morgan-Hughes JA. Holt IJ, et al. Hum Genet. 1988 May;79(1):53-7. doi: 10.1007/BF00291710. Hum Genet. 1988. PMID: 2896621

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

3

Prenatal diagnosis of mitochondrial DNA8993 T----G disease.

Harding AE, Holt IJ, Sweeney MG, Brockington M, Davis MB. Harding AE, et al. Among authors: holt ij. Am J Hum Genet. 1992 Mar;50(3):629-33. Am J Hum Genet. 1992. PMID: 1539598 Free PMC article.

4

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

5

Mitochondrial DNA analysis in Parkinson's disease.

Schapira AH, Holt IJ, Sweeney M, Harding AE, Jenner P, Marsden CD. Schapira AH, et al. Among authors: holt ij. Mov Disord. 1990;5(4):294-7. doi: 10.1002/mds.870050406. Mov Disord. 1990. PMID: 1979656

6

Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA.

McShane MA, Hammans SR, Sweeney M, Holt IJ, Beattie TJ, Brett EM, Harding AE. McShane MA, et al. Among authors: holt ij. Am J Hum Genet. 1991 Jan;48(1):39-42. Am J Hum Genet. 1991. PMID: 1985462 Free PMC article.

7

A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.

Holt IJ, Harding AE, Petty RK, Morgan-Hughes JA. Holt IJ, et al. Am J Hum Genet. 1990 Mar;46(3):428-33. Am J Hum Genet. 1990. PMID: 2137962 Free PMC article.

8

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: holt ij. 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

9

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

10

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: holt ij. Biochem Soc Trans. 1990 Aug;18(4):519-22. doi: 10.1042/bst0180519. Biochem Soc Trans. 1990. PMID: 2276422 Review. No abstract available.

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