Chalmers RM - Search Results

1

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.

2

Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.

Luoma P, Melberg A, Rinne JO, Kaukonen JA, Nupponen NN, Chalmers RM, Oldfors A, Rautakorpi I, Peltonen L, Majamaa K, Somer H, Suomalainen A. Luoma P, et al. Among authors: chalmers rm. Lancet. 2004 Sep 4-10;364(9437):875-82. doi: 10.1016/S0140-6736(04)16983-3. Lancet. 2004. PMID: 15351195

3

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.

4

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

5

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

6

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

7

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.

8

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

9

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.

10

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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