Sweeney MG - Search Results

1

Evidence against an X-linked locus close to DXS7 determining visual loss susceptibility in British and Italian families with Leber hereditary optic neuropathy.

Sweeney MG, Davis MB, Lashwood A, Brockington M, Toscano A, Harding AE. Sweeney MG, et al. Am J Hum Genet. 1992 Oct;51(4):741-8. Am J Hum Genet. 1992. PMID: 1415219 Free PMC article.

2

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. Am J Hum Genet. 1991 Jan;48(1):39-42. Am J Hum Genet. 1991. PMID: 1985462 Free PMC article.

3

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. Among authors: sweeney mg. Brain. 1992 Aug;115 ( Pt 4):979-89. doi: 10.1093/brain/115.4.979. Brain. 1992. PMID: 1393514

4

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

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

5

Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation.

Harding AE, Sweeney MG, Govan GG, Riordan-Eva P. Harding AE, et al. Among authors: sweeney mg. Am J Hum Genet. 1995 Jul;57(1):77-86. Am J Hum Genet. 1995. PMID: 7611298 Free PMC article.

6

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. Among authors: sweeney mg. Am J Hum Genet. 1995 May;56(5):1026-33. Am J Hum Genet. 1995. PMID: 7726155 Free PMC article.

7

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: sweeney mg. Brain. 1995 Apr;118 ( Pt 2):319-37. doi: 10.1093/brain/118.2.319. Brain. 1995. PMID: 7735876

8

A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies.

Brockington M, Sweeney MG, Hammans SR, Morgan-Hughes JA, Harding AE. Brockington M, et al. Among authors: sweeney mg. Nat Genet. 1993 May;4(1):67-71. doi: 10.1038/ng0593-67. Nat Genet. 1993. PMID: 8513327

9

Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy.

Chalmers RM, Davis MB, Sweeney MG, Wood NW, Harding AE. Chalmers RM, et al. Among authors: sweeney mg. Am J Hum Genet. 1996 Jul;59(1):103-8. Am J Hum Genet. 1996. PMID: 8659512 Free PMC article.

10

Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene.

Lee MJ, Stephenson DA, Groves MJ, Sweeney MG, Davis MB, An SF, Houlden H, Salih MA, Timmerman V, de Jonghe P, Auer-Grumbach M, Di Maria E, Scaravilli F, Wood NW, Reilly MM. Lee MJ, et al. Among authors: sweeney mg. Hum Mol Genet. 2003 Aug 1;12(15):1917-25. doi: 10.1093/hmg/ddg198. Hum Mol Genet. 2003. PMID: 12874111

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