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674 results

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The clinical spectrum of mitochondrial genetic disorders.
Kirkman MA, Yu-Wai-Man P, Chinnery PF. Kirkman MA, et al. Among authors: chinnery pf. Clin Med (Lond). 2008 Dec;8(6):601-6. doi: 10.7861/clinmedicine.8-6-601. Clin Med (Lond). 2008. PMID: 19149282 Free PMC article. No abstract available.
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.
Mitochondrial medicine.
Chinnery PF, Turnbull DM. Chinnery PF, et al. QJM. 1997 Nov;90(11):657-67. doi: 10.1093/qjmed/90.11.657. QJM. 1997. PMID: 9474346 Review. No abstract available.
Mitochondrial genotype and clinical phenotype.
Chinnery PF, Turnbull DM. Chinnery PF, et al. J Inherit Metab Dis. 1998 Jun;21(4):321-5. doi: 10.1023/a:1005357221101. J Inherit Metab Dis. 1998. PMID: 9700589 Review. No abstract available.
Mitochondrial DNA and disease.
Chinnery PF, Turnbull DM. Chinnery PF, et al. Lancet. 1999 Jul;354 Suppl 1:SI17-21. doi: 10.1016/s0140-6736(99)90244-1. Lancet. 1999. PMID: 10437851 Review. No abstract available.
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.
In-vitro genetic modification of mitochondrial function.
Taylor RW, Chinnery PF, Turnbull DM, Lightowlers RN. Taylor RW, et al. Among authors: chinnery pf. Hum Reprod. 2000 Jul;15 Suppl 2:79-85. doi: 10.1093/humrep/15.suppl_2.79. Hum Reprod. 2000. PMID: 11041515 Review.
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.
674 results