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Progressive myoclonic ataxia (the Ramsay Hunt syndrome).
Marsden CD, Harding AE, Obeso JA, Lu CS. Marsden CD, et al. Among authors: harding ae. Arch Neurol. 1990 Oct;47(10):1121-5. doi: 10.1001/archneur.1990.00530100091019. Arch Neurol. 1990. PMID: 2121121
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
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. Among authors: harding ae. Brain. 1993 Jun;116 ( Pt 3):617-32. doi: 10.1093/brain/116.3.617. Brain. 1993. PMID: 8513395
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: harding ae. Brain. 1995 Apr;118 ( Pt 2):319-37. doi: 10.1093/brain/118.2.319. Brain. 1995. PMID: 7735876
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.
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. Among authors: harding ae. Ann Neurol. 1995 Mar;37(3):400-3. doi: 10.1002/ana.410370317. Ann Neurol. 1995. PMID: 7695240
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. Among authors: harding ae. Brain. 1995 Jun;118 ( Pt 3):721-34. doi: 10.1093/brain/118.3.721. Brain. 1995. PMID: 7600089
Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA.
Holt IJ, Harding AE, Cooper JM, Schapira AH, Toscano A, Clark JB, Morgan-Hughes JA. Holt IJ, et al. Among authors: harding ae. Ann Neurol. 1989 Dec;26(6):699-708. doi: 10.1002/ana.410260603. Ann Neurol. 1989. PMID: 2604380
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