Harding AE - Search Results

1

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. Among authors: harding ae. Brain. 1992 Apr;115 ( Pt 2):343-65. doi: 10.1093/brain/115.2.343. Brain. 1992. PMID: 1606473

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

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.

5

Kearns-Sayre syndrome associated with mitochondrial DNA deletion or duplication: a molecular genetic and pathological study.

Brockington M, Alsanjari N, Sweeney MG, Morgan-Hughes JA, Scaravilli F, Harding AE. Brockington M, et al. Among authors: harding ae. J Neurol Sci. 1995 Jul;131(1):78-87. doi: 10.1016/0022-510x(95)00091-f. J Neurol Sci. 1995. PMID: 7561952

6

Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype.

Morgan-Hughes JA, Sweeney MG, Cooper JM, Hammans SR, Brockington M, Schapira AH, Harding AE, Clark JB. Morgan-Hughes JA, et al. Among authors: harding ae. Biochim Biophys Acta. 1995 May 24;1271(1):135-40. doi: 10.1016/0925-4439(95)00020-5. Biochim Biophys Acta. 1995. PMID: 7599199 Free article.

7

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

8

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

9

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation.

Riordan-Eva P, Sanders MD, Govan GG, Sweeney MG, Da Costa J, Harding AE. Riordan-Eva P, et al. Among authors: harding ae. Brain. 1995 Apr;118 ( Pt 2):319-37. doi: 10.1093/brain/118.2.319. Brain. 1995. PMID: 7735876

10

The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias.

Giunti P, Sweeney MG, Spadaro M, Jodice C, Novelletto A, Malaspina P, Frontali M, Harding AE. Giunti P, et al. Among authors: harding ae. Brain. 1994 Aug;117 ( Pt 4):645-9. doi: 10.1093/brain/117.4.645. Brain. 1994. PMID: 7922453 Free article.

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