Morgan-Hughes JA - Search Results

1

New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation.

Pulkes T, Liolitsa D, Eunson LH, Rose M, Nelson IP, Rahman S, Poulton J, Marchington DR, Landon DN, Debono AG, Morgan-Hughes JA, Hanna MG. Pulkes T, et al. Among authors: morgan hughes ja. Neuromuscul Disord. 2005 May;15(5):364-71. doi: 10.1016/j.nmd.2005.01.006. Neuromuscul Disord. 2005. PMID: 15833431

2

Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutation.

Hanna MG, Nelson I, Sweeney MG, Cooper JM, Watkins PJ, Morgan-Hughes JA, Harding AE. Hanna MG, et al. Am J Hum Genet. 1995 May;56(5):1026-33. Am J Hum Genet. 1995. PMID: 7726155 Free PMC article.

3

Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A-->G (MERRF) mutation: relationship to proportion of mutant mitochondrial DNA.

Hanna MG, Nelson IP, Morgan-Hughes JA, Harding AE. Hanna MG, et al. J Neurol Sci. 1995 Jun;130(2):154-60. doi: 10.1016/0022-510x(95)00022-t. J Neurol Sci. 1995. PMID: 8586979

4

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. Am J Hum Genet. 1998 Jul;63(1):29-36. doi: 10.1086/301910. Am J Hum Genet. 1998. PMID: 9634511 Free PMC article.

5

Fifty year follow-up of a patient with central core disease shows slow but definite progression.

Lamont PJ, Dubowitz V, Landon DN, Davis M, Morgan-Hughes JA. Lamont PJ, et al. Among authors: morgan hughes ja. Neuromuscul Disord. 1998 Aug;8(6):385-91. doi: 10.1016/s0960-8966(98)00043-1. Neuromuscul Disord. 1998. PMID: 9713855

6

MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity.

Hanna MG, Nelson IP, Morgan-Hughes JA, Wood NW. Hanna MG, et al. Among authors: morgan hughes ja. J Neurol Neurosurg Psychiatry. 1998 Oct;65(4):512-7. doi: 10.1136/jnnp.65.4.512. J Neurol Neurosurg Psychiatry. 1998. PMID: 9771776 Free PMC article.

7

The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS.

Pulkes T, Eunson L, Patterson V, Siddiqui A, Wood NW, Nelson IP, Morgan-Hughes JA, Hanna MG. Pulkes T, et al. Among authors: morgan hughes ja. Ann Neurol. 1999 Dec;46(6):916-9. doi: 10.1002/1531-8249(199912)46:6<916::aid-ana16>3.0.co;2-r. Ann Neurol. 1999. PMID: 10589546

8

A novel mutation in the mitochondrial tRNA(TYr) gene associated with exercise intolerance.

Pulkes T, Siddiqui A, Morgan-Hughes JA, Hanna MG. Pulkes T, et al. Among authors: morgan hughes ja. Neurology. 2000 Oct 24;55(8):1210-2. doi: 10.1212/wnl.55.8.1210. Neurology. 2000. PMID: 11071502

9

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. Brain. 1995 Jun;118 ( Pt 3):721-34. doi: 10.1093/brain/118.3.721. Brain. 1995. PMID: 7600089

10

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. Ann Neurol. 1995 Mar;37(3):400-3. doi: 10.1002/ana.410370317. Ann Neurol. 1995. PMID: 7695240

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