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243 results
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Hereditary motor and sensory neuropathies and hereditary spastic paraplegia: a magnetic stimulation study.
Claus D, Waddy HM, Harding AE, Murray NM, Thomas PK. Claus D, et al. Among authors: harding ae. Ann Neurol. 1990 Jul;28(1):43-9. doi: 10.1002/ana.410280109. Ann Neurol. 1990. PMID: 2375632
Deficiency of respiratory chain complex I is a common cause of Leigh disease.
Morris AA, Leonard JV, Brown GK, Bidouki SK, Bindoff LA, Woodward CE, Harding AE, Lake BD, Harding BN, Farrell MA, Bell JE, Mirakhur M, Turnbull DM. Morris AA, et al. Among authors: harding ae, harding bn. Ann Neurol. 1996 Jul;40(1):25-30. doi: 10.1002/ana.410400107. Ann Neurol. 1996. PMID: 8687187
Cortical reflex myoclonus in patients with the mitochondrial DNA transfer RNA(Lys)(8344) (MERRF) mutation.
Thompson PD, Hammans SR, Harding AE. Thompson PD, et al. Among authors: harding ae. J Neurol. 1994 Mar;241(5):335-40. doi: 10.1007/BF00868443. J Neurol. 1994. PMID: 8006688
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
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
Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophy.
Holt IJ, Miller DH, Harding AE. Holt IJ, et al. Among authors: harding ae. J Neurol Neurosurg Psychiatry. 1988 Aug;51(8):1075-7. doi: 10.1136/jnnp.51.8.1075. J Neurol Neurosurg Psychiatry. 1988. PMID: 2905730 Free PMC article.
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
Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.
Holt IJ, Miller DH, Harding AE. Holt IJ, et al. Among authors: harding ae. J Med Genet. 1989 Dec;26(12):739-43. doi: 10.1136/jmg.26.12.739. J Med Genet. 1989. PMID: 2575667 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: harding ae. Brain. 1992 Apr;115 ( Pt 2):343-65. doi: 10.1093/brain/115.2.343. Brain. 1992. PMID: 1606473
Striatal D1 and D2 dopamine receptor loss in asymptomatic mutation carriers of Huntington's disease.
Weeks RA, Piccini P, Harding AE, Brooks DJ. Weeks RA, et al. Among authors: harding ae. Ann Neurol. 1996 Jul;40(1):49-54. doi: 10.1002/ana.410400110. Ann Neurol. 1996. PMID: 8687191
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