Koenig M. K.
Presentation and diagnosis of mitochondrial disorders in children. Pediatr Neurol. 2008 May; 38(5):305–13. doi:10.1016/j.pediatr-neurol.2007.12.001.Li H., et al.
Comparative bioenergetic study of neuronal and muscle mitochondria during aging. Free Radic Biol Med. 2013 Oct; 63:30–40. Epub Apr 30 2013. doi:10.1016/j.freeradbiomed.2013.04.030.Lodi R., et al.
Antioxidant treatment improves in vivo cardiac and skeletal muscle bioenergetics in patients with Friedreich’s ataxia. Ann Neurol. 2001 May 1; 49(5):590–6. doi:10.1002/ana.1001.McFarland R., Taylor R. W, Turnbull D. M.
A neurological perspective on mitochondrial disease. Lancet Neurol. 2010 Aug; 9(8):829–840. doi:10.1016/S1474-4422(10)70116-2.Siciliano G., et al.
Functional diagnostics in mitochondrial diseases. Biosci Rep. 2007 Jun; 27(1–3):53–67. doi:10.1007/s10540-007-9037-0.Sproule D. M., Kaufmann P.
Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome. Ann NY Acad Sci. 2008 Oct; 1142:133–58. doi:10.1196/annals.1444.011.Tarnopolsky M. A, Raha S
. Mitochondrial myopathies: diagnosis, exercise intolerance, and treatment options. Med Sci Sports Exerc. 2005 Dec; 37(12):2086–93.Taylor R. W., Turnbull D. M.
Mitochondrial DNA mutations in human disease. Nat Rev Genet. 2005 May; 6(5):389–402. doi:10.1038/nrg1606.Thorburn D. R.
Mitochondrial disorders: prevalence, myths and advances. J Inherit Metab Dis. 2004; 27(3):349–62. doi:10.1023/ B: BOLI.0000031098.41409.55.Tuppen H. A., et al.
Mitochondrial DNA mutations and human disease. Biochim Biophys Acta. 2010 Feb; 1797(2):113–28. doi:10.1016/j.bba-bio.2009.09.005.Uitto J., Bernstein E. F.
Molecular mechanisms of cutaneous aging: connective tissue alterations in the dermis. J Investig Dermatol Symp Proc. 1998 Aug; 3(1):41–4.Waller J. M., Maibach H. I.
Age and skin structure and function, a quantitative approach (II): protein, glycosaminoglycan, water, and lipid content and structure. Skin Res Technol. 2006 Aug; 12(3):145–54. doi:10.1111/j.0909752X.2006.00146.x.Возрастная тугоухость
Bai U., et al.
Mitochondrial DNA deletions associated with aging and possibly presbycusis: a human archival temporal bone study. Am J Otol. 1997 Jul;18(4):449–53.Chen F. Q., et al.
Mitochondrial peroxiredoxin 3 regulates sensory cell survival in the cochlea. PLoS One. 2013 Apr 23; 8(4):e61999. doi:10.1371/ journal.pone.0061999.Dahl H. H., et al.
Etiology and audiological outcomes at 3 years for 364 children in Australia. PLoS One. 2013;8(3):e59624. Epub 2013 Mar 28. doi:10.1371/journal.pone.0059624.Ding Y., et al.
The role of mitochondrial DNA mutations in hearing loss. Biochem Genet. 2013 Aug;51(7–8):588–602. Epub Apr 21 2013. doi:10.1007/s10528-013-9589-6.Granville D. J., Gottlieb R. A.
Mitochondria: Regulators of cell death and survival. Scientific World Journal. 2002 Jun 11; 2:1569–78. doi:10.1100/ tsw.2002.809.Han C., Someya S.
Maintaining good hearing: calorie restriction, Sirt3, and glutathione. Exp Gerontol. 2013 Oct 1; 48(10):1091–5. Epub 2013 Feb 20. doi:10.1016/j.exger.2013.02.014. Johnsson L. G., Hawkins J. E. Jr. Vascular changes in the human inner ear associated with aging. Ann Otol Rhinol Laryngol. 1972 Jun; 81(3):364–76. doi:10.1177/000348947208100307.Komlosi K., et al.
Non-syndromic hearing impairment in a Hungarian family with the m.7510T>C mutation of mitochondrial tRNA(Ser(UCN)) and review of published cases. JIMD Rep. 2013; 9:105–11. Epub 2012 Nov 2. doi:10.1007/8904_2012_187.Lin F. R., et al.
Hearing loss and cognitive decline in older adults. JAMA Intern Med. 2013; 173(4):293–9. doi:10.1001/jamainternmed.2013.1868. Luo L. F., Hou C. C., Yang W. X. Nuclear factors: roles related to mitochondrial deafness. Gene. 2013 May 15;520(2):79–89. Epub 2013 Mar 17. doi:10.1016/j.gene.2013.03.041.Miller J. M., Marks N. J., Goodwin P. C.
Laser Doppler measurements of cochlear blood flow. Hearing Res. 1983 Sep;11(3):385–94.Seidman M. D.
Effects of dietary restriction and antioxidants on presbycusis. Laryngoscope. 2000 May;110(5 pt 1):727–38. doi:10.1097/00005537-200005000-00003.