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102 results
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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.
Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA.
Reardon W, Ross RJ, Sweeney MG, Luxon LM, Pembrey ME, Harding AE, Trembath RC. Reardon W, et al. Among authors: sweeney mg. Lancet. 1992 Dec 5;340(8832):1376-9. doi: 10.1016/0140-6736(92)92560-3. Lancet. 1992. PMID: 1360090
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
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.
Late onset Leber's optic neuropathy: a case confused with ischaemic optic neuropathy.
Borruat FX, Green WT, Graham EM, Sweeney MG, Morgan-Hughes JA, Sanders MD. Borruat FX, et al. Among authors: sweeney mg. Br J Ophthalmol. 1992 Sep;76(9):571-3. doi: 10.1136/bjo.76.9.571. Br J Ophthalmol. 1992. PMID: 1420066 Free PMC article.
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.
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: sweeney mg. Brain. 1992 Apr;115 ( Pt 2):343-65. doi: 10.1093/brain/115.2.343. Brain. 1992. PMID: 1606473
Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples.
Hammans SR, Sweeney MG, Brockington M, Morgan-Hughes JA, Harding AE. Hammans SR, et al. Among authors: sweeney mg. Lancet. 1991 Jun 1;337(8753):1311-3. doi: 10.1016/0140-6736(91)92981-7. Lancet. 1991. PMID: 1674297
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. Among authors: sweeney m. Am J Hum Genet. 1991 Jan;48(1):39-42. Am J Hum Genet. 1991. PMID: 1985462 Free PMC article.
Mitochondrial myopathies: genetic defects.
Harding AE, Holt IJ, Cooper JM, Schapira AH, Sweeney M, Clark JB, Morgan-Hughes JA. Harding AE, et al. Among authors: sweeney m. Biochem Soc Trans. 1990 Aug;18(4):519-22. doi: 10.1042/bst0180519. Biochem Soc Trans. 1990. PMID: 2276422 Review. No abstract available.
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