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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. Am J Hum Genet. 1996 Jul;59(1):103-8. Am J Hum Genet. 1996. PMID: 8659512 Free PMC article.
Debrisoquine hydroxylase polymorphism in Leber's hereditary optic neuropathy.
Chalmers RM, Bandmann O, Harding AE. Chalmers RM, et al. J Neurol Neurosurg Psychiatry. 1996 May;60(5):588. doi: 10.1136/jnnp.60.5.588. J Neurol Neurosurg Psychiatry. 1996. PMID: 8778272 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. J Neurol Sci. 1996 Feb;135(2):173-5. doi: 10.1016/0022-510x(95)00286-b. J Neurol Sci. 1996. PMID: 8867075
Sequence of mitochondrial DNA in patients with multiple sclerosis.
Chalmers RM, Robertson N, DAS Compston, Harding AE. Chalmers RM, et al. Ann Neurol. 1996 Aug;40(2):239-43. doi: 10.1002/ana.410400216. Ann Neurol. 1996. PMID: 8773606
Clinical, biochemical and molecular genetic features of Leber's hereditary optic neuropathy.
Chalmers RM, Schapira AH. Chalmers RM, et al. Biochim Biophys Acta. 1999 Feb 9;1410(2):147-58. doi: 10.1016/s0005-2728(98)00163-7. Biochim Biophys Acta. 1999. PMID: 10076023 Review.
A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndrome.
Chalmers RM, Lamont PJ, Nelson I, Ellison DW, Thomas NH, Harding AE, Hammans SR. Chalmers RM, et al. Neurology. 1997 Aug;49(2):589-92. doi: 10.1212/wnl.49.2.589. Neurology. 1997. PMID: 9270602
Autosomal recessive inheritance of hereditary motor and sensory neuropathy with optic atrophy.
Chalmers RM, Riordan-Eva P, Wood NW. Chalmers RM, et al. J Neurol Neurosurg Psychiatry. 1997 Apr;62(4):385-7. doi: 10.1136/jnnp.62.4.385. J Neurol Neurosurg Psychiatry. 1997. PMID: 9120454 Free PMC article.
Mitochondrial encephalopathy with multiple mitochondrial DNA deletions: a report of two families and two sporadic cases with unusual clinical and neuropathological features.
Chalmers RM, Brockington M, Howard RS, Lecky BR, Morgan-Hughes JA, Harding AE. Chalmers RM, et al. J Neurol Sci. 1996 Nov;143(1-2):41-5. doi: 10.1016/s0022-510x(96)00032-9. J Neurol Sci. 1996. PMID: 8981296
Autosomal dominant optic atrophy with asymptomatic peripheral neuropathy.
Chalmers RM, Bird AC, Harding AE. Chalmers RM, et al. J Neurol Neurosurg Psychiatry. 1996 Feb;60(2):195-6. doi: 10.1136/jnnp.60.2.195. J Neurol Neurosurg Psychiatry. 1996. PMID: 8708653 Free PMC article.
Sequence of the human homologue of a mitochondrially encoded murine transplantation antigen in patients with multiple sclerosis.
Chalmers RM, Robertson N, Kellar-Wood H, Compston DA, Harding AE. Chalmers RM, et al. J Neurol. 1995 May;242(5):332-4. doi: 10.1007/BF00878877. J Neurol. 1995. PMID: 7643143
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