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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: harding ae. Am J Hum Genet. 1996 Jul;59(1):103-8. Am J Hum Genet. 1996. PMID: 8659512 Free PMC article.
Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.
Mackey DA, Oostra RJ, Rosenberg T, Nikoskelainen E, Bronte-Stewart J, Poulton J, Harding AE, Govan G, Bolhuis PA, Norby S. Mackey DA, et al. Among authors: harding ae. Am J Hum Genet. 1996 Aug;59(2):481-5. Am J Hum Genet. 1996. PMID: 8755941 Free PMC article. No abstract available.
HLA class I genotypes in Leber's hereditary optic neuropathy.
Chalmers RM, Govan GG, Schapira AH, Harding AE. Chalmers RM, et al. Among authors: harding ae. J Neurol Sci. 1996 Feb;135(2):173-5. doi: 10.1016/0022-510x(95)00286-b. J Neurol Sci. 1996. PMID: 8867075
HLA class II genotypes in Leber's hereditary optic neuropathy.
Govan GG, Smith PR, Kellar-Wood H, Schapira AH, Harding AE. Govan GG, et al. Among authors: harding ae. J Neurol Sci. 1994 Nov;126(2):193-6. doi: 10.1016/0022-510x(94)90272-0. J Neurol Sci. 1994. PMID: 7853025
Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis.
Kellar-Wood H, Robertson N, Govan GG, Compston DA, Harding AE. Kellar-Wood H, et al. Among authors: harding ae. Ann Neurol. 1994 Jul;36(1):109-12. doi: 10.1002/ana.410360121. Ann Neurol. 1994. PMID: 8024249
Platelet mitochondrial function in Leber's hereditary optic neuropathy.
Smith PR, Cooper JM, Govan GG, Harding AE, Schapira AH. Smith PR, et al. Among authors: harding ae. J Neurol Sci. 1994 Mar;122(1):80-3. doi: 10.1016/0022-510x(94)90055-8. J Neurol Sci. 1994. PMID: 8195807
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.
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: harding ae. Am J Hum Genet. 1991 Jan;48(1):39-42. Am J Hum Genet. 1991. PMID: 1985462 Free PMC article.
Mitochondrial DNA mutation underlying Leigh's syndrome: clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsy.
Sweeney MG, Hammans SR, Duchen LW, Cooper JM, Schapira AH, Kennedy CR, Jacobs JM, Youl BD, Morgan-Hughes JA, Harding AE. Sweeney MG, et al. Among authors: harding ae. J Neurol Sci. 1994 Jan;121(1):57-65. doi: 10.1016/0022-510x(94)90157-0. J Neurol Sci. 1994. PMID: 8133313
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: harding ae. Am J Hum Genet. 1995 May;56(5):1026-33. Am J Hum Genet. 1995. PMID: 7726155 Free PMC article.
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