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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
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
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
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
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
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.
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.
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
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
Mammalian mitochondrial genetics: heredity, heteroplasmy and disease.
Lightowlers RN, Chinnery PF, Turnbull DM, Howell N. Lightowlers RN, et al. Among authors: chinnery pf. Trends Genet. 1997 Nov;13(11):450-5. doi: 10.1016/s0168-9525(97)01266-3. Trends Genet. 1997. PMID: 9385842 Review.
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