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1Academic Journal
Authors: А. К. Семенчук
Source: Žurnal Grodnenskogo Gosudarstvennogo Medicinskogo Universiteta, Vol 23, Iss 1, Pp 49-54 (2025)
Subject Terms: плазма, прерывистая алкогольная интоксикация, метионин, гомоцистеин, гипергомоцистеинемия, Medicine
File Description: electronic resource
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2Academic Journal
Source: Высшая школа: научные исследования.
Subject Terms: гипергомоцистеинемия, недифференцированная дисплазия соединительной ткани (НДСТ), ангиовит, гомоцистеин сыворотки
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3Academic Journal
Authors: Эльвира Константиновна Гребенникова, Сергей Васильевич Гребенников, Марина Яковлевна Домрачева, Татьяна Алексеевна Соколова-Попова, Наталья Михайловна Яметова, Ольга Александровна Домрачева, Анна Сергеевна Вишневская
Source: Мать и дитя в Кузбассе, Vol 25, Iss 3, Pp 99-104 (2024)
Subject Terms: фолиевая кислота, метафолин, гипергомоцистеинемия, дефекты нервной трубки плода, прегравидарная подготовка, Pediatrics, RJ1-570, Gynecology and obstetrics, RG1-991
File Description: electronic resource
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4Academic Journal
Authors: Гайбуллаева , Динара
Source: Eurasian Journal of Academic Research; Vol. 5 No. 11 (2025): Eurasian Journal of Academic Research; 35-42 ; Евразийский журнал академических исследований; Том 5 № 11 (2025): Евразийский журнал академических исследований; 35-42 ; Yevrosiyo ilmiy tadqiqotlar jurnali; Jild 5 Nomeri 11 (2025): Евразийский журнал академических исследований; 35-42 ; 2181-2020
Subject Terms: Преэклампсия, гипергомоцистеинемия, С-реактивный белок, фактор Виллебрандта, биофизический профиль плода, задержка внутриутробного роста, Preelampsia, hyperhomocysteinemia, C-reactive protein, Willebrandt factor, fetal biophysical profile, intrauterine growth retardation, Preeklampsiya, gipergomotsisteinemiya, C-reaktiv oqsil, Villebrandt omili, homilaning biofizik profili, bachadon ichidagi o’sishning kechikishi
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Availability: https://in-academy.uz/index.php/ejar/article/view/65690
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5
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6
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7Academic Journal
Source: Мать и дитя в Кузбассе, Vol 25, Iss 3, Pp 99-104 (2024)
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8Academic Journal
Authors: Гребенникова, Эльвира Константиновна, Гребенников, Сергей Васильевич, Домрачева, Марина Яковлевна, Соколова-Попова, Татьяна Алексеевна, Яметова, Наталья Михайловна, Домрачева, Ольга Александровна, Вишневская, Анна Сергеевна
Source: Mother and Baby in Kuzbass; № 3 (2024): сентябрь; 99-104 ; Мать и Дитя в Кузбассе; № 3 (2024): сентябрь; 99-104 ; 2542-0968 ; 1991-010X
Subject Terms: folic acid, metafolin, hyperhomocysteinemia, fetal neural tube defects, pre-conception preparation of women, фолиевая кислота, метафолин, гипергомоцистеинемия, дефекты нервной трубки плода, прегравидарная подготовка
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Relation: http://mednauki.ru/index.php/MD/article/view/1101/1918; http://mednauki.ru/index.php/MD/article/view/1101/1938; http://mednauki.ru/index.php/MD/article/view/1101
Availability: http://mednauki.ru/index.php/MD/article/view/1101
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9Academic Journal
Authors: A. P. Sazonova, Yu. P. Milyutina, O. N. Bespalova, O. V. Pachuliia, I. V. Zalozniaia, A. V. Korenevsky, А. П. Сазонова, Ю. П. Милютина, О. Н. Беспалова, О. В. Пачулия, И. В. Залозняя, А. В. Кореневский
Source: Obstetrics, Gynecology and Reproduction; Vol 18, No 5 (2024); 658–666 ; Акушерство, Гинекология и Репродукция; Vol 18, No 5 (2024); 658–666 ; 2500-3194 ; 2313-7347
Subject Terms: ГГЦ, 5-methyltetrahydrofolate, 5-MTHF, experimental model, folate cycle, hyperhomocysteinemia, HHC, 5-метилтетрагидрофолат, экспериментальная модель, фолатный цикл, гипергомоцистеинемия
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Relation: https://www.gynecology.su/jour/article/view/2227/1257; Seremak-Mrozikiewicz A. Metafolin – alternative for folate deficiency supplementation in pregnant women. Ginekol Pol. 2013;84(7):641–6. https://doi.org/10.17772/gp/1618.; Cochrane K.M., Mayer C., Devlin A.M. et al. Is natural (6S)-5-methyltetrahydrofolic acid as effectiveas synthetic folic acid in increasing serum and red blood cell folate concentrations during pregnancy? A proof-of-concept pilot study. Trials. 2020;21(1):380. https://doi.org/10.1186/s13063-020-04320-3.; Pietrzik K., Bailey L., Shane B. Folic acid and L-5-methyltetrahydrofolate: comparison of clinical pharmacokinetics and pharmacodynamics. Clin Pharmacokinet. 2010;49(8):535–48. https://doi.org/10.2165/11532990-000000000-00000.; Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. Lancet. 1991;338(8760):131–7. https://doi.org/10.1016/0140-6736(91)90133-A.; Czeizel A.E., Dudas I., Paput L., Banhidy F. Prevention of neural-tube defects with periconceptional folic acid, methylfolate, or multivitamins? Ann Nutr Metab. 2011;58(4):263–71. https://doi.org/10.1159/000330776.; U.S. Preventive Services Task Force. Folic acid for the prevention of neural tube defects: U.S. Preventive Services Task Force recommendation statement. Ann Intern Med. 2009;150(9):626–31. https://doi.org/10.7326/0003-4819-150-9-200905050-00009.; Quinn M., Halsey J., Sherliker P. et al. Global heterogeneity in folic acid fortification policies and implications for prevention of neural tube defects and stroke: a systematic review. ЕClinicalMedicine. 2023;67:102366. https://doi.org/10.1016/j.eclinm.2023.102366.; Tang J.S., Cait A., White R.M. et al. MR1-dependence of unmetabolized folic acid side-effects. Front Immunol. 2022;3:946713. https://doi.org/10.3389/fimmu.2022.946713.; Kalmbach R., Paul L., Selhub J. Determination of unmetabolized folic acid in human plasma using affinity HPLC. Am J Clin Nutr. 2011;94(1):343S–347S. https://doi.org/10.3945/ajcn.111.013433.; Chen P., Tang L., Song Y. et al. Association of folic acid dosage with circulating unmetabolized folic acid in Chinese adults with H-type hypertension: a multicenter, double-blind, randomized controlled trial. Front Nutr. 2023;10:1191610. https://doi.org/10.3389/fnut.2023.1191610.; Dai C., Fei Y., Li J. A novel review of homocysteine and pregnancy complications. BioMed Res Int. 2021;2021:6652231. https://doi.org/10.1155/2021/6652231.; Clare C.E., Brassington A.H., Kwong W.Y., Sinclair K.D. One-carbon metabolism: linking nutritional biochemistry to epigenetic programming of long-term development. Annu Rev Anim Biosci. 2019;7:263–87. https://doi.org/10.1146/annurev-animal-020518-115206.; Visentin M., Diop-Bove N., Zhao R., Goldman I.D. The intestinal absorption of folates. Annu Rev Physiol. 2014;76:251–74. https://doi.org/10.1146/annurev-physiol-020911-153251.; Duthie S.J., Narayanan S., Blum S. et al. Folate deficiency in vitro induces uracil misincorporation and DNA hypomethylation and inhibits DNA excision repair in immortalized normal human colon epithelial cells. Nutr Cancer. 2000;37(2):245–51. https://doi.org/10.1207/S15327914NC372_18.; Kelly P., McPartlin J., Goggins M. et al. Unmetabolized folic acid in serum: acute studies in subjects consuming fortified food and supplements. Am J Clin Nutrition. 1997;65(6):1790–5. https://doi.org/10.1093/ajcn/65.6.1790.; Shane B. Folate chemistry and metabolism. In: Folate in health and disease. Ed. L. Bailey. N.Y.: Marcel Dekker, 2017. 1–22.; Matherly L.H., Goldman D.I. Membrane transport of folates. Vitam Horm. 2003;66:403–56. https://doi.org/10.1016/s0083-6729(03)01012-4.; Koury M.J., Ponka P. New insights into erythropoiesis: the roles of folate, vitamin B12, andiron. Annu Rev Nutr. 2004;24:105–31. https://doi.org/10.1146/annurev.nutr.24.012003.132306.; Керкешко Г.О., Арутюнян А.В., Аржанова О.Н., Милютина Ю.П. Оптимизация терапии фолатами при осложнениях беременности. Журнал акушерства и женских болезней. 2013;62(6):25–36.; Hoss G.R.W., Sperb-Ludwig F., Schwartz I.V.D, Blom H.J. Classical homocystinuria: a common inborn error of metabolism? An epidemiological study based on genetic databases. Mol Genet Genomic Med. 2020;8(6):1214. https://doi.org/10.1002/mgg3.1214.; Korokin M.V., Pokrovskiy M.V., Novikov O.O. et al. A model of hyperhomocysteine-induced endothelial dysfunction in rats. Bull Exp Biol Med. 2011;152(2):213–5. https://doi.org/10.1007/s10517-011-1491-9.; Zhuo J.M., Praticò D. Normalization of hyperhomocysteinemia improves cognitive deficits and ameliorates brain amyloidosis of a transgenic mouse model of Alzheimer’s disease. FASEB J. 2010;24(10):3895–902. https://doi.org/10.1096/fj.10-161828.; Милютина Ю.П., Пустыгина А.В., Щербицкая А.Д. и др. Сравнение показателей окислительного стресса в сыворотке крови крыс при различных моделях гипергомоцистеинемии. Acta Biomedica Scientifica. 2016;1(3–2):120–3.; Зильфян В.Н., Кумкумаджян В.А. Новый метод взятия крови у мелких лабораторных животных. Журнал экспериментальной и клинической медицины. 1970:10(4):12–4.; https://www.gynecology.su/jour/article/view/2227
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10Academic Journal
Authors: Анна Сергеевна Вишневская
Source: Мать и дитя в Кузбассе, Vol 25, Iss 3, Pp 99-104 (2024)
Subject Terms: фолиевая кислота, метафолин, гипергомоцистеинемия, дефекты нервной трубки плода, прегравидарная подготовка, Pediatrics, RJ1-570, Gynecology and obstetrics, RG1-991
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11Academic Journal
Authors: M. S. Balashova, Sh. Mutallibzoda, D. A. Velina, O. B. Shvabskaya, V. V. Gorbachev, I. A. Nikitin
Source: Кардиоваскулярная терапия и профилактика, Vol 22, Iss 9 (2023)
Subject Terms: фолатный цикл, гипергомоцистеинемия, полиморфизм генов, метилфолат, метилкобаламин, пиридоксина гидрохлорид, персонализированное питание, искусственные нейронные сети, Diseases of the circulatory (Cardiovascular) system, RC666-701
File Description: electronic resource
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12Academic Journal
Source: Лабораторная диагностика. Восточная Европа. :238-251
Subject Terms: 2. Zero hunger, methylmalonic acid, holotranscobalamin, vitamin B12, homocysteine, витамин В12, 3. Good health, 03 medical and health sciences, 0302 clinical medicine, vegetarianism, гомоцистеин, гипергомоцистеинемия, голотранскобаламин, hyperhomocysteinemia, вегетарианство, метилмалоновая кислота
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13Academic Journal
Authors: A. K. Semenchuk, V. V. Lelevich
Source: Žurnal Grodnenskogo Gosudarstvennogo Medicinskogo Universiteta, Vol 19, Iss 2, Pp 170-175 (2021)
Subject Terms: плазма, прерывистая алкогольная интоксикация, метионин, гомоцистеин, гипергомоцистеинемия, Medicine
File Description: electronic resource
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14Academic Journal
Authors: V. O. Bitsadze, E. V. Slukhanchuk, A. G. Solopova, J. Kh. Khizroeva, D. V. Shcherbakov, F. E. Yakubova, J.-C. Gris, I. Elalamy, N. D. Degtyareva, A. V. Lazarchuk, M. A. Gileva, N. V. Samburova, Z. D. Aslanova, D. V. Blinov, A. S. Shkoda, A. D. Makatsariya, В. О. Бицадзе, Е. В. Слуханчук, А. Г. Солопова, Д. Х. Хизроева, Д. В. Щербаков, Ф. Э. Якубова, Ж.-К. Гри, И. Элалами, Н. Д. Дегтярева, А. В. Лазарчук, М. А. Гилева, Н. В. Самбурова, З. Д. Асланова, Д. В. Блинов, А. С. Шкода, А. Д. Макацария
Source: Obstetrics, Gynecology and Reproduction; Vol 17, No 4 (2023); 390-401 ; Акушерство, Гинекология и Репродукция; Vol 17, No 4 (2023); 390-401 ; 2500-3194 ; 2313-7347
Subject Terms: фолатный цикл, homocysteine, HC, hyperhomocysteinemia, HHC, oncothrombosis, folic acid, folate cycle, гомоцистеин, ГЦ, гипергомоцистеинемия, ГГЦ, онкотромбозы, фолиевая кислота
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Relation: https://www.gynecology.su/jour/article/view/1761/1129; Alcalay A., Wun T., Khatri V. et al. Venous thromboembolism in patients with colorectal cancer: incidence and effect on survival. J Clin Oncol. 2006;24(7):1112–8. https://doi.org/10.1200/JCO.2005.04.2150.; Khorana A.A., Francis C.W., Culakova E. et al. Frequency, risk factors, and trends for venous thromboembolism among hospitalized cancer patients. Cancer. 2007;110(10):2339–46. https://doi.org/10.1002/cncr.23062.; Sharma G.S., Kumar T., Dar T.A., Singh L.R. Protein N-homocysteinylation: From cellular toxicity to neurodegeneration. Biochim Biophys Acta. 2015;1850:2239–45. https://doi.org/10.1016/j.bbagen.2015.08.013.; Brustolin S., Giugliani R., Felix T.M. Genetics of homocysteine metabolism and associated disorders. Braz J Med Biol Res. 2010;43(1):1–7. https://doi.org/10.1590/s0100-879x2009007500021.; Seshadri S. Elevated plasma homocysteine levels: risk factor or risk marker for the development of dementia and Alzheimer's disease? J Alzheimer's Dis. 2006;9(4):393–8. https://doi.org/10.3233/jad-2006-9404.; Mancardi D., Penna C., Merlino A. et al. Physiological and pharmacological features of the novel gasotransmitter: hydrogen sulfide. Biochim Biophys Acta. 2009;1787(7):864–72. https://doi.org/10.1016/j.bbabio.2009.03.005.; Wu L.L., Wu J.T. Hyperhomocysteinemia is a risk factor for cancer and a new potential tumor marker. Clin Chim Acta. 2002;322(1–2):21–8. https://doi.org/10.1016/s0009-8981(02)00174-2.; Seshadri S., Beiser A., Selhub J. et al. Plasma homocysteine as a risk factor for dementia and Alzheimer's disease. N Engl J Med. 2002;346(7):476–83. https://doi.org/10.1056/NEJMoa011613.; Selhub J. Homocysteine metabolism. Annu Rev Nutr. 1999;19:217–46. https://doi.org/10.1146/annurev.nutr.19.1.217.; Jacques P.F., Bostom A.G., Williams R.R. et al. Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations. Circulation. 1996;93(1):7–9. https://doi.org/10.1161/01.cir.93.1.7.; Williams K.T., Schalinske K.L. New insights into the regulation of methyl group and homocysteine metabolism. J Nutr. 2007;137(2):311–4. https://doi.org/10.1093/jn/137.2.311.; Locasale J.W. Serine, glycine and one-carbon units: cancer metabolism in full circle. Nat Rev Cancer. 2013;13(8):572–83. https://doi.org/10.1038/nrc3557.; Zhang S.M., Willett W.C., Selhub J. et al. Plasma folate, vitamin B6, vitamin B12, homocysteine, and risk of breast cancer. J Natl Cancer Inst. 2003;95(5):373–80. https://doi.org/10.1093/jnci/95.5.373.; Siniscalchi A., Mancuso F., Gallelli L. et al. Increase in plasma homocysteine levels induced by drug treatments in neurologic patients Pharmacol Res. 2005;52(5):367–75. https://doi.org/10.1016/j.phrs.2005.05.013.; Hjelt K., Brynskov J., Hippe E. et al. Oral contraceptives and the cobalamin (vitamin B12) metabolism. Acta Obstet Gynecol Scand. 1985;64(1):59–63. https://doi.org/10.3109/00016348509154689.; Matsuo K., Hamajima N., Hirai T. et al. Methionine synthase reductase gene A66G polymorphism is associated with risk of colorectal cancer. Asian Pac J Cancer Prev. 2002;3(4):353–9.; Obwegeser R., Hohlagschwandtner M., Sinzinger H. Homocysteine – a pathophysiological cornerstone in obstetrical and gynaecological disorders? Hum Reprod Update. 1999;5(1):64–72. https://doi.org/10.1093/humupd/5.1.64.; Montfort W.R., Perry K.M., Fauman E.B. et al. Structure, multiple site binding, and segmental accommodation in thymidylate synthase on binding dUMP and an anti-folate. Biochemistry. 1990;29(30):6964–77. https://doi.org/10.1021/bi00482a004.; Blount B.C., Mack M.M., Wehr C.M. et al. Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damage. Proc Natl Acad Sci U S A. 1997;94(7):3290–5. https://doi.org/10.1073/pnas.94.7.3290.; Hay R.K., Park J.-G., Gazdar A. Atlas of human tumor cell lines. Academic Press, 2013. 490; Crider K.S., Yang T.P., Berry R.J., Bailey L.B. Folate and DNA methylation: a review of molecular mechanisms and the evidence for folate's role. Adv Nutr. 2012;3(1):21–38. https://doi.org/10.3945/an.111.000992.; Hall L.E., Mitchell S.E, O’Neill R.J. Pericentric and centromeric transcription: a perfect balance required. Chromosome Res. 2012;20(5):535–46. https://doi.org/10.1007/s10577-012-9297-9.; Ehrlich M. DNA hypomethylation, cancer, the immunodeficiency, centromeric region instability, facial anomalies syndrome and chromosomal rearrangements. J Nutr. 2002;132(8 Suppl):2424S–2429S. https://doi.org/10.1093/jn/132.8.2424S.; Zhang D., Wen X., Wu W. et al. Elevated homocysteine level and folate deficiency associated with increased overall risk of carcinogenesis: metaanalysis of 83 case-control studies involving 35,758 individuals. PLoS One. 2015;10(5):e0123423. https://doi.org/10.1371/journal.pone.0123423.; Stathopoulou A., Vlachonikolis I., Mavroudis D. et al. Molecular detection of cytokeratin-19-positive cells in the peripheral blood of patients with operable breast cancer: Evaluation of their prognostic significance. J Clin Oncol. 2002;20(16):3404–12. https://doi.org/10.1200/JCO.2002.08.135.; Mcdonald L., Bray C., Field C. et al. Homocystinuria, thrombosis, and the blood-platelets. Lancet. 1964;1(7336):745–6. https://doi.org/10.1016/s0140-6736(64)92852-1.; Tonetti C., Amiel J., Munnich A., Zittoun J. Impact of new mutations in the methylenetetrahydrofolate reductase gene assessed on biochemical phenotypes: a familial study. J Inherit Metab Dis. 2001;24(8):833–42. https://doi.org/10.1023/a:1013988123902.; Sibani S., Christensen B., O'Ferrall E. et al. Characterization of six novel mutations in the methylenetetrahydrofolate reductase (MTHFR) gene in patients with homocystinuria. Hum Mutat. 2000;15(3):280–7. https://doi.org/10.1002/(SICI)1098-1004(200003)15:33.0.CO;2-I.; Kluijtmans L.A., Wendel U., Stevens E. et al. Identification of four novel mutations in severe methylenetetrahydrofolate reductase deficiency. Eur J Hum Genet. 1998;6(3):257–65. https://doi.org/10.1038/sj.ejhg.5200182.; Brezovska-Kavrakova J., Krstevska M., Bosilkova G. et al. Hyperhomocysteinemia and of methylenetetrahydrofolate reductase (C677T) genetic polymorphism in patients with deep vein thrombosis. Mater Sociomed. 2013;25(3):170–4. https://doi.org/10.5455/msm.2013.25.170-174.; van der Put N.M., Steegers-Theunissen R.P., Frosst P. et al. Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida. Lancet. 1995;346(8982):1070–1. https://doi.org/10.1016/s0140-6736(95)91743-8.; Robien K., Ulrich C.M. 5, 10-Methylenetetrahydrofolate reductase polymorphisms and leukemia risk: a HuGE minireview. Am J Epidemiol. 2003;157(7):571–82. https://doi.org/10.1093/aje/kwg024.; Weisberg I.S., Jacques P.F., Selhub J. et al. The 1298A→ C polymorphism in methylenetetrahydrofolate reductase (MTHFR): in vitro expression and association with homocysteine. Atherosclerosis. 2001;156(2):409–15. https://doi.org/10.1016/s0021-9150(00)00671-7.; Alberg A.J., Selhub J., Shah K.V. et al. The risk of cervical cancer in relation to serum concentrations of folate, vitamin B12, and homocysteine. Cancer Epidemiol Biomarkers Prev. 2000;9(7):761–4.; Powers H.J. Interaction among folate, riboflavin, genotype, and cancer, with reference to colorectal and cervical cancer. J Nutr. 2005;135(12 Suupl):2960S–2966S. https://doi.org/10.1093/jn/135.12.2960S.; Gatt A., Makris A., Cladd H. et al. Hyperhomocysteinemia in women with advanced breast cancer. Int J Lab Hematol. 2007;29(6):421–5. https://doi.org/10.1111/j.1751-553X.2007.00907.x.; Heit J.A., O'Fallon W.M., Petterson T.M. et al. Relative impact of risk factors for deep vein thrombosis and pulmonary embolism: a populationbased study. Arch Intern Med. 2002;162(11):1245–8. https://doi.org/10.1001/archinte.162.11.1245.; Welch G.N., Loscalzo J. Homocysteine and atherothrombosis. N Engl J Med. 1998;338(15):1042–50. https://doi.org/10.1056/NEJM199804093381507.; Sharma G.S., Kumar T., Singh L.R. N-homocysteinylation induces different structural and functional consequences on acidic and basic proteins. PLoS One. 2014;9:e116386. https://doi.org/10.1371/journal.pone.0116386.; Kumar T., Sharma G.S., Singh L.R. Homocystinuria: therapeutic approach. Clin Chim Acta. 2016;458:55–62. https://doi.org/10.1016/j.cca.2016.04.002.; Lentz S.R., Sobey C.G., Piegors D.J. et al. Vascular dysfunction in monkeys with diet-induced hyperhomocyst (e) inemia. J Clin Invest. 1996;98(1):24–9. https://doi.org/10.1172/JCI118771.; FitzGerald G.A. Parsing an enigma: the pharmacodynamics of aspirin resistance. Lancet. 2003;361(9357):542–4. https://doi.org/10.1016/S0140-6736(03)12560-3.; Sibrian-Vazquez M., Escobedo J.O., Lim S. et al. Homocystamides promote free-radical and oxidative damage to proteins. Proc Natl Acad Sci U S A. 2010;107(2):551–4. https://doi.org/10.1073/pnas.0909737107.; Zhang J.-.W, Yan R., Tang Y.-S. et al. Hyperhomocysteinemia-induced autophagy and apoptosis with downregulation of hairy enhancer of split 1/5 in cortical neurons in mice. Int J Immunopathol Pharmacol. 2017;30(4):371–82. https://doi.org/10.1177/0394632017740061.; Škovierová H., Vidomanová E., Mahmood S. et al. The molecular and cellular effect of homocysteine metabolism imbalance on human health. Int J Mol Sci. 2016;17(10):1733. https://doi.org/10.3390/ijms17101733.; Biron F., Rousseau J., Baulin J. et al. Thromboembolic event and metabolic hyperhomocysteinemia: A case report and review of literature. Ann Cardiol Angeiol (Paris). 2021;70(3):177–82. (In French). https://doi.org/10.1016/j.ancard.2021.01.008.; Aday A.W., Duran E.K, Van Denburgh M. et al. Homocysteine is associated with future venous thromboembolism in 2 prospective cohorts of women. Arterioscler Thromb Vasc Biol. 2021;41(7):2215–24. https://doi.org/10.1161/ATVBAHA.121.316397.; https://www.gynecology.su/jour/article/view/1761
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15Academic Journal
Authors: Жиляева, Т.В., Смирнова, А.Г., Благонравова, А.С., Мазо, Г.Э.
Source: Современная терапия психических расстройств, Vol 2020, Iss 2 (53), Pp 39-47 (2020)
Subject Terms: шизофрения, дефицит фолатов, гипергомоцистеинемия, коморбидность, дизонтогенез, schizophrenia, folate deficiency, hyperhomocysteinemia, comorbidity, dysontogenesis, Neurology. Diseases of the nervous system, RC346-429, Medicine
File Description: electronic resource
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16Academic Journal
Authors: Андрей Глебович Васильев, Ксения Владимировна Морозова, Татьяна Викторовна Брус, Михаил Маркович Забежинский, Алефтина Алексеевна Кравцова, Лев Дмитриевич Балашов, Анна Валентиновна Васильева, Сарнг Саналович Пюрвеев, Анна Николаевна Косова
Source: Российские биомедицинские исследования, Vol 7, Iss 1 (2022)
Subject Terms: гомоцистеин, беременность, гипергомоцистеинемия, тромбоз, витамин В12, фолиевая кислота, Medicine (General), R5-920
File Description: electronic resource
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17Academic Journal
Authors: Коломиец, Т. В., Зерчанинова, Е. И., Градобоев, Д. С., Ким, М. В.
Subject Terms: TRANSIENT DISORDERS OF CEREBRAL CIRCULATION, CLINICAL CASE, THROMBOPHILIA, YOUNG AGE, HYPERHOMOCYSTEINEMIA, ПРЕХОДЯЩИЕ НАРУШЕНИЕ МОЗГОВОГО КРОВООБРАЩЕНИЯ, КЛИНИЧЕСКИЙ СЛУЧАЙ, ТРОМБОФИЛИЯ, МОЛОДОЙ ВОЗРАСТ, ГИПЕРГОМОЦИСТЕИНЕМИЯ
File Description: application/pdf
Relation: Тенденции развития науки и образования. – 2022. – № 87-1.; http://elib.usma.ru/handle/usma/9168
Availability: http://elib.usma.ru/handle/usma/9168
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18Academic Journal
Authors: Ф.Х., Иноятова, З.Ч., Курбонова, Ш.А., Бабаджанова
Source: PEDAGOG; Vol. 5 No. 6 (2022): PEDAGOG; 564-579
Subject Terms: MTHFR, полиморфизми, rs 1801131, rs 1801133, ёввойи аллел, минор аллел фолат цикли, гипергомоцистеинемия, эндотелиал дисфункция
File Description: application/pdf
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19Academic Journal
Authors: Ф.Х, Иноятова, З.Ч, Курбонова, Ш.А, Бабаджанова
Source: O'ZBEKISTONDA FANLARARO INNOVATSIYALAR VA ILMIY TADQIQOTLAR JURNALI; Vol. 2 No. 13 (2022): O'ZBEKISTONDA FANLARARO INNOVATSIYALAR VA ILMIY TADQIQOTLAR JURNALI; 208-227 ; 2181-3302
Subject Terms: MTR, MTRR, rs1805087, rs1801394, ёввойи аллел, минор аллел фолат цикли, гипергомоцистеинемия, эндотелиал дисфункция
File Description: application/pdf
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20Academic Journal
Source: Российские биомедицинские исследования, Vol 7, Iss 1 (2022)
Subject Terms: Medicine (General), тромбоз, R5-920, фолиевая кислота, гомоцистеин, гипергомоцистеинемия, витамин В12, беременность