Taylor RW - Search Results

1

An unusual case of congenital muscular dystrophy with normal serum CK level, external ophtalmoplegia, and white matter changes on brain MRI.

Vondracek P, Hermanova M, Vodickova K, Fajkusova L, Blakely EL, He L, Turnbull DM, Taylor RW, Tajsharghi H. Vondracek P, et al. Among authors: taylor rw. Eur J Paediatr Neurol. 2007 Nov;11(6):381-4. doi: 10.1016/j.ejpn.2007.01.010. Epub 2007 Mar 29. Eur J Paediatr Neurol. 2007. PMID: 17395506

2

Complex aetiology of type 2 diabetes.

Walker M, Taylor R, Armstrong M, Turnbull DM. Walker M, et al. Br J Hosp Med. 1994 Aug 17-Sep 6;52(4):179. Br J Hosp Med. 1994. PMID: 8000686 No abstract available.

3

Succinate-cytochrome c reductase: assessment of its value in the investigation of defects of the respiratory chain.

Taylor RW, Birch-Machin MA, Bartlett K, Turnbull DM. Taylor RW, et al. Biochim Biophys Acta. 1993 Jun 19;1181(3):261-5. doi: 10.1016/0925-4439(93)90030-5. Biochim Biophys Acta. 1993. PMID: 8391327

4

MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNA.

Taylor RW, Chinnery PF, Haldane F, Morris AA, Bindoff LA, Wilson J, Turnbull DM. Taylor RW, et al. Ann Neurol. 1996 Sep;40(3):459-62. doi: 10.1002/ana.410400318. Ann Neurol. 1996. PMID: 8797538

5

Deficiency of complex II of the mitochondrial respiratory chain in late-onset optic atrophy and ataxia.

Taylor RW, Birch-Machin MA, Schaefer J, Taylor L, Shakir R, Ackrell BA, Cochran B, Bindoff LA, Jackson MJ, Griffiths P, Turnbull DM. Taylor RW, et al. Among authors: taylor l. Ann Neurol. 1996 Feb;39(2):224-32. doi: 10.1002/ana.410390212. Ann Neurol. 1996. PMID: 8967754

6

Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acids.

Taylor RW, Chinnery PF, Turnbull DM, Lightowlers RN. Taylor RW, et al. Nat Genet. 1997 Feb;15(2):212-5. doi: 10.1038/ng0297-212. Nat Genet. 1997. PMID: 9020853

7

A novel mitochondrial tRNA phenylalanine mutation presenting with acute rhabdomyolysis.

Chinnery PF, Johnson MA, Taylor RW, Lightowlers RN, Turnbull DM. Chinnery PF, et al. Among authors: taylor rw. Ann Neurol. 1997 Mar;41(3):408-10. doi: 10.1002/ana.410410319. Ann Neurol. 1997. PMID: 9066365

8

Treatment of mitochondrial disease.

Taylor RW, Chinnery PF, Clark KM, Lightowlers RN, Turnbull DM. Taylor RW, et al. J Bioenerg Biomembr. 1997 Apr;29(2):195-205. doi: 10.1023/a:1022646215643. J Bioenerg Biomembr. 1997. PMID: 9239544 Review.

9

A novel mitochondrial tRNA isoleucine gene mutation causing chronic progressive external ophthalmoplegia.

Chinnery PF, Johnson MA, Taylor RW, Durward WF, Turnbull DM. Chinnery PF, et al. Among authors: taylor rw. Neurology. 1997 Oct;49(4):1166-8. doi: 10.1212/wnl.49.4.1166. Neurology. 1997. PMID: 9339712

10

A novel mitochondrial DNA point mutation in the tRNA(Ile) gene: studies in a patient presenting with chronic progressive external ophthalmoplegia and multiple sclerosis.

Taylor RW, Chinnery PF, Bates MJ, Jackson MJ, Johnson MA, Andrews RM, Turnbull DM. Taylor RW, et al. Biochem Biophys Res Commun. 1998 Feb 4;243(1):47-51. doi: 10.1006/bbrc.1997.8055. Biochem Biophys Res Commun. 1998. PMID: 9473477

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