Harding AE - Search Results

1

Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.

Holt IJ, Miller DH, Harding AE. Holt IJ, et al. Among authors: harding ae. J Med Genet. 1989 Dec;26(12):739-43. doi: 10.1136/jmg.26.12.739. J Med Genet. 1989. PMID: 2575667 Free PMC article.

2

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

3

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

4

Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophy.

Holt IJ, Miller DH, Harding AE. Holt IJ, et al. Among authors: harding ae. J Neurol Neurosurg Psychiatry. 1988 Aug;51(8):1075-7. doi: 10.1136/jnnp.51.8.1075. J Neurol Neurosurg Psychiatry. 1988. PMID: 2905730 Free PMC article.

5

Bilateral simultaneous optic neuropathy in adults: clinical, imaging, serological, and genetic studies.

Morrissey SP, Borruat FX, Miller DH, Moseley IF, Sweeney MG, Govan GG, Kelly MA, Francis DA, Harding AE, McDonald WI. Morrissey SP, et al. Among authors: harding ae. J Neurol Neurosurg Psychiatry. 1995 Jan;58(1):70-4. doi: 10.1136/jnnp.58.1.70. J Neurol Neurosurg Psychiatry. 1995. PMID: 7823072 Free PMC article.

6

Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation.

Harding AE, Sweeney MG, Miller DH, Mumford CJ, Kellar-Wood H, Menard D, McDonald WI, Compston DA. Harding AE, et al. Brain. 1992 Aug;115 ( Pt 4):979-89. doi: 10.1093/brain/115.4.979. Brain. 1992. PMID: 1393514

7

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

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

8

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: harding ae. Mov Disord. 1990;5(4):294-7. doi: 10.1002/mds.870050406. Mov Disord. 1990. PMID: 1979656

9

A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.

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

10

Molecular genetics of amyloid neuropathy in Europe.

Holt IJ, Harding AE, Middleton L, Chrysostomou G, Said G, King RH, Thomas PK. Holt IJ, et al. Among authors: harding ae. Lancet. 1989 Mar 11;1(8637):524-6. doi: 10.1016/s0140-6736(89)90068-8. Lancet. 1989. PMID: 2564060

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