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A case-control study of Leber's hereditary optic neuropathy.
Charlmers RM, Harding AE. Charlmers RM, et al. Brain. 1996 Oct;119 ( Pt 5):1481-6. doi: 10.1093/brain/119.5.1481. Brain. 1996. PMID: 8931573
HLA class I genotypes in Leber's hereditary optic neuropathy.
Chalmers RM, Govan GG, Schapira AH, Harding AE. Chalmers RM, et al. 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. 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. 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. J Neurol Sci. 1994 Mar;122(1):80-3. doi: 10.1016/0022-510x(94)90055-8. J Neurol Sci. 1994. PMID: 8195807
Clinical and laboratory findings in referrals for mitochondrial DNA analysis.
Lamont PJ, Surtees R, Woodward CE, Leonard JV, Wood NW, Harding AE. Lamont PJ, et al. Among authors: harding ae. Arch Dis Child. 1998 Jul;79(1):22-7. doi: 10.1136/adc.79.1.22. Arch Dis Child. 1998. PMID: 9771247 Free PMC article.
The mitochondrial DNA transfer RNA(Lys)A-->G(8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF). Relationship of clinical phenotype to proportion of mutant mitochondrial DNA.
Hammans SR, Sweeney MG, Brockington M, Lennox GG, Lawton NF, Kennedy CR, Morgan-Hughes JA, Harding AE. Hammans SR, et al. Brain. 1993 Jun;116 ( Pt 3):617-32. doi: 10.1093/brain/116.3.617. Brain. 1993. PMID: 8513395
Mitochondrial genes and neurological disease.
Harding AE. Harding AE. Clin Exp Neurol. 1993;30:1-16. Clin Exp Neurol. 1993. PMID: 7712619 Review. No abstract available.
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