1. Butrova S.A. Metabolicheskiy sindrom: patogenez, klinika, diagnostika, podhody k lecheniyu. RMZh, 2001, № 2, s. 56-60. @@[Butrova S.A. Metabolic syndrome: pathogenesis, clinical features, diagnosis, treatment approaches. RMJ, 2001, no. 2, pp. 56-60. (In Russ.)]
2. Saklayen M.G. The Global Epidemic of the Metabolic Syndrome. Curr. Hypertens. Rep., 2018, vol. 20, no. 2, p. 12, DOI:https://doi.org/10.1007/s11906-018-0812-z. EDN: https://elibrary.ru/VFJEKJ
3. Aydin S., Aksoy A., Aydin S., Kalayci M., Yilmaz M., Kuloglu T., Citil C., Catak Z. Today's and yesterday's of pathophysiology: biochemistry of metabolic syndrome and animal models. Nutrition, 2014, vol. 30, no. 1, pp. 1-9, DOI:https://doi.org/10.1016/j.nut.2013.05.013.
4. Chawla A., Chawla R., Jaggi S. Microvasular and macrovascular complications in diabetes mellitus: Distinct or continuum? Indian J. Endocrinol. Metab., 2016, vol. 20, no. 4, pp. 546-551, DOI:https://doi.org/10.4103/2230-8210.183480.
5. Gyawali P., Richards R.S., Bwititi P.T., Nwose E.U. Association of abnormal erythrocyte morphology with oxidative stress and inflammation in metabolic syndrome. Blood Cells Mol. Dis., 2015, vol. 54, no. 4, pp. 360-363. DOI:https://doi.org/10.1016/j.bcmd.2015.01.005. EDN: https://elibrary.ru/XOIHLB
6. Lang P.A., Kaiser S., Myssina S., Wieder T., Lang F., Huber S. M. Role of Ca2+-activated K+ channels in human erythrocyte apoptosis. Am. J. Physiol. Cell Physiol., 2003, vol. 285, no. 6, pp. C1553-S1560. DOI:https://doi.org/10.1152/ajpcell. 00186.2003. DOI: https://doi.org/10.1152/ajpcell.00186.2003; EDN: https://elibrary.ru/MCJBLT
7. Huisjes R., Bogdanova A., van Solinge W.W., Schiffelers R.M., Kaestner L., van Wijk R. Squeezing for Life - Properties of Red Blood Cell Deformability. Front Physiol., 2018, no. 9, p. 656. DOI: 3389/fphys.2018.00656.
8. Bogdanova A., Berenbrink M., Nikinmaa M. Oxygen-dependent ion transport in erythrocytes. Acta Physiol. (Oxf.), 2009, vol. 195, no. 3, pp. 305-319, DOI:https://doi.org/10.1111/j.1748-1716.2008.01934.x. EDN: https://elibrary.ru/MMWVGB
9. Kennett E.C., Kuchel P.W. Redox Reactions and Electron Transfer Across the Red Cell Membrane. IUBMB Life, 2003, vol. 55, no. 7, rp. 375-385. DOI:https://doi.org/10.1080/15216540310001592843.
10. Srinivas S.P., Bonanno J.A., Lariviere E., Jans D, Van Driessche W. Measurement of rapid changes in cell volume by forward light scattering. Pflugers Archive: European Journal of Physiology, 2003, vol. 447, no. 1, pp. 97-108. DOI:https://doi.org/10.1007/s00424-003-1145-5. EDN: https://elibrary.ru/ESQCSJ
11. Orlov S.N., Petrova I.V., Pokudin N.I., Baskakov M.B., Medvedev M.A. Ca2+-aktiviruemye kalievye kanaly eritrocitov, issledovannye metodom registracii Sa2+-inducirovannyh izmeneniy membrannogo potenciala. Biol. membrany: Zhurn. membr. i klet. biol., 1992, № 9 (9), s. 885-903 @@[Orlov S.N., Petrova I.V., Pokudin N.I., Baskakov M.B., Medvedev M.A. Ca2+-activated potassium channels of erythrocytes, studied by the method of recording the Ca2+-induced changes in the membrane potential. Biochemistry (Moscow) Supplement. Series A: Membrane and Cell Biology, 1992, vol. 9, no. 9, pp. 885-903. (In Russ.)]
12. Mahindrakar Y.S., Suryakar A.N., Ankush R.D., Katkam R.V., Kumbhar K.M. Comparison Between Erythrocyte Hemoglobin and Spectrin Glycosylation and Role of Oxidative Stress in type-2 Diabetes Mellitus. Indian J. Clin. Biochem., 2007, vol. 22, no. 1, pp. 91-94, DOI:https://doi.org/10.1007/BF02912888.
13. Lu Y., Liu J. Erythrocyte membrane proteins and membrane skeleton. Front. Biol. China, 2007, no. 2, pp. 247-255, DOI:https://doi.org/10.1007/s11515-007-0035-1. EDN: https://elibrary.ru/SYUWXF
14. Birulina Yu.G., Petrova I.V., Rozenbaum Yu.A., Shefer E.A., Smagliy L.V., Nosarev A.V., Gusakova S.V. Izmeneniya ob'ema eritrocitov, oposredovannye serovodorodom: rol' Gardos-kanalov, Na+, K+, 2CL--kotransporta i anionnogo obmennika. Byull. eksp. biol. i med., 2019, t. 167, № 4, s. 497-500. @@[Birulina Y.G., Petrova I.V., Rozenbaum Y.A., Shefer E.A., Smagliy L.V., Nosarev A.V., Gusakova S.V. H2S-Mediated Changes in Erythrocyte Volume: Role of Gardos Channels, Na+, K+,2Cl- Cotransport and Anion Exchanger. Bull. Exp. Biol. Med., 2019, no 7, pp. 508-511 (In Russ.)]. EDN: https://elibrary.ru/ZBEUXR
15. Lang F. Mechanisms and significance of cell volume regulation. J. Am. Coll. Nutr., 2007, vol. 26 (5 Suppl.), pp. 613S-623S, DOI:https://doi.org/10.1080/07315724.2007.10719667. EDN: https://elibrary.ru/MKYXWD



