Harding AE - Search Results

1

The clinical features of mitochondrial myopathy.

Petty RK, Harding AE, Morgan-Hughes JA. Petty RK, et al. Among authors: harding ae. Brain. 1986 Oct;109 ( Pt 5):915-38. doi: 10.1093/brain/109.5.915. Brain. 1986. PMID: 3779373

2

Mitochondrial myopathy: a genetic study of 71 cases.

Harding AE, Petty RK, Morgan-Hughes JA. Harding AE, et al. J Med Genet. 1988 Aug;25(8):528-35. doi: 10.1136/jmg.25.8.528. J Med Genet. 1988. PMID: 3050098 Free PMC article. Review.

3

The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study.

Hammans SR, Sweeney MG, Hanna MG, Brockington M, Morgan-Hughes JA, Harding AE. Hammans SR, et al. Among authors: harding ae. Brain. 1995 Jun;118 ( Pt 3):721-34. doi: 10.1093/brain/118.3.721. Brain. 1995. PMID: 7600089

4

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

5

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.

Holt IJ, Harding AE, Morgan-Hughes JA. Holt IJ, et al. Among authors: harding ae. Nature. 1988 Feb 25;331(6158):717-9. doi: 10.1038/331717a0. Nature. 1988. PMID: 2830540

6

Mitochondrial DNA polymorphism in mitochondrial myopathy.

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

7

Deletions of muscle mitochondrial DNA.

Holt IJ, Cooper JM, Morgan-Hughes JA, Harding AE. Holt IJ, et al. Among authors: harding ae. Lancet. 1988 Jun 25;1(8600):1462. doi: 10.1016/s0140-6736(88)92273-8. Lancet. 1988. PMID: 2898614 No abstract available.

8

The retinal manifestations of mitochondrial myopathy. A study of 22 cases.

Mullie MA, Harding AE, Petty RK, Ikeda H, Morgan-Hughes JA, Sanders MD. Mullie MA, et al. Among authors: harding ae. Arch Ophthalmol. 1985 Dec;103(12):1825-30. doi: 10.1001/archopht.1985.01050120059020. Arch Ophthalmol. 1985. PMID: 4074172

9

A new mitochondrial DNA mutation associated with progressive dementia and chorea: a clinical, pathological, and molecular genetic study.

Nelson I, Hanna MG, Alsanjari N, Scaravilli F, Morgan-Hughes JA, Harding AE. Nelson I, et al. Among authors: harding ae. Ann Neurol. 1995 Mar;37(3):400-3. doi: 10.1002/ana.410370317. Ann Neurol. 1995. PMID: 7695240

10

The mitochondrial DNA transfer RNA(Lys)A-->G(8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF). Relationship of clinical phenotype to proportion of mutant mitochondrial DNA.

Hammans SR, Sweeney MG, Brockington M, Lennox GG, Lawton NF, Kennedy CR, Morgan-Hughes JA, Harding AE. Hammans SR, et al. Among authors: harding ae. Brain. 1993 Jun;116 ( Pt 3):617-32. doi: 10.1093/brain/116.3.617. Brain. 1993. PMID: 8513395

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