Chinnery PF - Search Results

1

A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysis.

McFarland R, Taylor RW, Chinnery PF, Howell N, Turnbull DM. McFarland R, et al. Among authors: chinnery pf. Neuromuscul Disord. 2004 Feb;14(2):162-6. doi: 10.1016/j.nmd.2003.10.011. Neuromuscul Disord. 2004. PMID: 14733964

2

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. Among authors: chinnery pf. Ann Neurol. 1996 Sep;40(3):459-62. doi: 10.1002/ana.410400318. Ann Neurol. 1996. PMID: 8797538

3

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. Among authors: chinnery pf. Nat Genet. 1997 Feb;15(2):212-5. doi: 10.1038/ng0297-212. Nat Genet. 1997. PMID: 9020853

4

A novel mitochondrial tRNA phenylalanine mutation presenting with acute rhabdomyolysis.

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

5

Maternally inherited diabetes and deafness: prevalence in a hospital diabetic population.

Newkirk JE, Taylor RW, Howell N, Bindoff LA, Chinnery PF, Alberti KG, Turnbull DM, Walker M. Newkirk JE, et al. Among authors: chinnery pf. Diabet Med. 1997 Jun;14(6):457-60. doi: 10.1002/(SICI)1096-9136(199706)14:6<457::AID-DIA372>3.0.CO;2-W. Diabet Med. 1997. PMID: 9212310

6

Treatment of mitochondrial disease.

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

7

Recurrent strokes in a 34-year-old man.

Chinnery PF, Turnbull DM, Walls TJ, Reading PJ. Chinnery PF, et al. Lancet. 1997 Aug 23;350(9077):560. doi: 10.1016/s0140-6736(97)05005-8. Lancet. 1997. PMID: 9284779 No abstract available.

8

CSF antigliadin antibodies and the Ramsay Hunt syndrome.

Chinnery PF, Reading PJ, Milne D, Gardner-Medwin D, Turnbull DM. Chinnery PF, et al. Neurology. 1997 Oct;49(4):1131-3. doi: 10.1212/wnl.49.4.1131. Neurology. 1997. PMID: 9339701

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. Neurology. 1997 Oct;49(4):1166-8. doi: 10.1212/wnl.49.4.1166. Neurology. 1997. PMID: 9339712

10

Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes.

Chinnery PF, Howell N, Lightowlers RN, Turnbull DM. Chinnery PF, et al. Brain. 1997 Oct;120 ( Pt 10):1713-21. doi: 10.1093/brain/120.10.1713. Brain. 1997. PMID: 9365365

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