Chinnery PF - Search Results

1

A common UCP2 polymorphism predisposes to stress hyperglycaemia in severe sepsis.

Pyle A, Ibbett IM, Gordon C, Keers SM, Walker M, Chinnery PF, Baudouin SV. Pyle A, et al. Among authors: chinnery pf. J Med Genet. 2009 Nov;46(11):773-5. doi: 10.1136/jmg.2009.067173. Epub 2009 Jun 25. J Med Genet. 2009. PMID: 19556617 Free PMC article.

2

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

3

Mitochondrial diabetes: investigation and identification of a novel mutation.

Lynn S, Wardell T, Johnson MA, Chinnery PF, Daly ME, Walker M, Turnbull DM. Lynn S, et al. Among authors: chinnery pf. Diabetes. 1998 Nov;47(11):1800-2. doi: 10.2337/diabetes.47.11.1800. Diabetes. 1998. PMID: 9792552 No abstract available.

4

Nonrandom tissue distribution of mutant mtDNA.

Chinnery PF, Zwijnenburg PJ, Walker M, Howell N, Taylor RW, Lightowlers RN, Bindoff L, Turnbull DM. Chinnery PF, et al. Am J Med Genet. 1999 Aug 27;85(5):498-501. Am J Med Genet. 1999. PMID: 10405450

5

Mitochondrial DNA analysis: polymorphisms and pathogenicity.

Chinnery PF, Howell N, Andrews RM, Turnbull DM. Chinnery PF, et al. J Med Genet. 1999 Jul;36(7):505-10. J Med Genet. 1999. PMID: 10424809 Free PMC article. Review.

6

Clinical mitochondrial genetics.

Chinnery PF, Howell N, Andrews RM, Turnbull DM. Chinnery PF, et al. J Med Genet. 1999 Jun;36(6):425-36. J Med Genet. 1999. PMID: 10874629 Free PMC article. Review.

7

Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?

Chinnery PF, Andrews RM, Turnbull DM, Howell NN. Chinnery PF, et al. Am J Med Genet. 2001 Jan 22;98(3):235-43. doi: 10.1002/1096-8628(20010122)98:3<235::aid-ajmg1086>3.0.co;2-o. Am J Med Genet. 2001. PMID: 11169561

8

Epidemiology and treatment of mitochondrial disorders.

Chinnery PF, Turnbull DM. Chinnery PF, et al. Am J Med Genet. 2001 Spring;106(1):94-101. doi: 10.1002/ajmg.1426. Am J Med Genet. 2001. PMID: 11579428 Review.

9

Leber hereditary optic neuropathy.

Yu-Wai-Man P, Turnbull DM, Chinnery PF. Yu-Wai-Man P, et al. Among authors: chinnery pf. J Med Genet. 2002 Mar;39(3):162-9. doi: 10.1136/jmg.39.3.162. J Med Genet. 2002. PMID: 11897814 Free PMC article. Review.

10

Defining the importance of mitochondrial gene defects in maternally inherited diabetes by sequencing the entire mitochondrial genome.

Choo-Kang AT, Lynn S, Taylor GA, Daly ME, Sihota SS, Wardell TM, Chinnery PF, Turnbull DM, Walker M. Choo-Kang AT, et al. Among authors: chinnery pf. Diabetes. 2002 Jul;51(7):2317-20. doi: 10.2337/diabetes.51.7.2317. Diabetes. 2002. PMID: 12086967

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