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    Book

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    Relation: Обзорный цикл лекций по анатомии человека / О. А. Шерстюк, Н. Л. Свинцицкая, А. В. Пилюгин [и др.]. – Полтава, 2021. – 194 с.; https://repository.pdmu.edu.ua/handle/123456789/14928

  7. 7
    Academic Journal

    Source: Clinical anatomy and operative surgery; Vol. 3 No. 4 (2004); 42-48
    Клиническая анатомия и оперативная хирургия; Том 3 № 4 (2004); 42-48
    Клінічна анатомія та оперативна хірургія; Том 3 № 4 (2004); 42-48

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  8. 8
    Academic Journal

    Source: Neurology, Neuropsychiatry, Psychosomatics; Vol 13, No 1 (2021); 51-56 ; Неврология, нейропсихиатрия, психосоматика; Vol 13, No 1 (2021); 51-56 ; 2310-1342 ; 2074-2711 ; 10.14412/2074-2711-2021-1

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    Relation: https://nnp.ima-press.net/nnp/article/view/1507/1183; https://nnp.ima-press.net/nnp/article/view/1507/1184; Khoo A, Frasca J, Schultz D. Measuring disease activity and predicting response to intravenous immunoglobulin in chronic inflammatory demyelinating polyneuropathy. Biomark Res. 2019;7(1):1-8. doi:10.1186/s40364-0190154-2; Bril V, Blanchette CM, Noone JM, et al. The dilemma of diabetes in chronic inflammatory demyelinating polyneuropathy. J Diabetes Complicat. Sep-Oct 2016;30(7):1401-7. doi:10.1016/j.jdiacomp.2016.05.007. Epub 2016 May 10.; Broers MC, Bunschoten C, Nieboer D, et al. Incidence and Prevalence of Chronic Inflammatory Demyelinating Polyradiculoneuropathy: A Systematic Review and Meta-Analysis. Neuroepidemiology. 2019;52(3-4):161-72. doi:10.1159/000494291; Попова ТЕ, Шнайдер НА, Петрова ММ и др. Эпидемиология хронической воспалительной демиелинизирующей полиневропатии за рубежом и в России. Нервно-мышечные болезни. 2015;5(2):10-5. doi:10.17650/2222-8721-2015-5-2-10-15; Турсынов НИ, Григолашвили МА, Илюшина МЮ и др. Современные аспекты диагностики и лечения хронических демиелинизирующих полинейропатий. Нейрохирургия и неврология Казахстана. 2016;3(44):38-45.; Щукин ИА, Лебедева АВ, Чубыкин ВИ и др. Астения у пациентов с хроническими неврологическими заболеваниями. Клиницист. 2013;7(2):64-72. doi:10.17650/18188338-2013-2-64-72; Lawley A, Abbas A, Seri S, Rajabally YA. Clinical correlates of fatigue in chronic inflammatory demyelinating polyneuropathy. Muscle Nerve. 2020;62(2):226-32. doi:10.1002/mus.26913; Van den Bergh PYK, Hadden RDM, Bouche P, et al. European Federation of Neurological Societies/Peripheral Nerve Society Guideline on management of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint task force of the European Federation of Neurological Societies and the Peripher. Eur J Neurol. 2010;17(3):356-63. doi:10.1111/j.1468-1331.2009.02930.x; Dyck PJ, Davies JL, Litchy WJ, O'Brien PC. Longitudinal assessment of diabetic polyneuropathy using a composite score in the Rochester Diabetic Neuropathy Study cohort. Neurology. 1997;49(1):229-39. doi:10.1212/wnl.49.1.229; Kleyweg RP, Meche FGA, Schmitz PIM. Interobserver agreement in the assessment of muscle strength Guillain-Barre syndrome. Muscle Nerve. 1991 Nov;14(11):1103-9. doi:10.1002/mus.880141111; Alabdali M, Abraham A, Alsulaiman A, et al. Clinical characteristics, and impairment and disability scale scores for different CIDP Disease Activity Status classes. J Neurol Sci. 2017 Jan 15;372:223-7. doi:10.1016/j.jns.2016.11.056. Epub 2016 Nov 23.; Merkies ISJ, Kieseier BC. Fatigue, pain, anxiety and depression in Guillain-Barre syndrome and chronic inflammatory demyelinating polyradiculoneuropathy. Eur Neurol. 2016;75(3-4):199-206. doi:10.1159/000445347; Gavrilov YuV, Shkilnyuk GG, Valko PO, et al. Validation of the Russian Version of the Fatigue Impact Scale and Fatigue Severity Scale in multiple sclerosis patients. Acta Neurol Scand. 2018 Nov;138(5):408-416. doi:10.1111/ane.12993. Epub 2018 Jul 9.; Chaudhuri A, Behan P. Fatigue in neurological disorders. Lancet. 2004 Mar 20;363(9413):978-88. doi:10.1016/S01406736(04)15794-2; Zwarts MJ, Bleijenberg G, van Engelen BGM. Clinical neurophysiology of fatigue. Clin Neurophysiol. 2008 Jan;119(1):2-10. doi:10.1016/j.clinph.2007.09.126. Epub 2007 Nov 26.; Kent-Braun JA, Le Blanc R. Quantitation of Central Activation Failure During Maximal Volintary Contractions in Humans. Muscle Nerve. 1996 Jul;19(7):861-9. doi:10.1002/(SICI)10974598(199607)19:73.0.CO;2-7; Garssen MPJ, Schillings ML, van Doorn PA, et al. Contributions of Central and Peripheral Factors to Residual Fatigue in Guillain-Barre Syndrome. Muscle Nerve. 2007 Jul;36(1):93-9. doi:10.1002/mus.20739; Boukhris S, Magy L, Gallouedec G, et al. Fatigue as the main presenting symptom of chronic inflammatory demyelinating polyradiculoneuropathy: A study of 11 cases. J Peripher Nerv Syst. 2005 Sep;10(3):329-37. doi:10.1111/j.1085-9489.2005.10311.x; Westblad ME, Forsberg A, Press R. Disability and health status in patients with chronic inflammatory demyelinating polyneuropathy. Disabil Rehabil. 2009;31(9):720-5. doi:10.1080/09638280802306497; Gable KL, Attarian H, Allen JA. Fatigue in chronic inflammatory demyelinating polyneuropathy. Muscle Nerve. 2020 Dec;62(6):673-80. doi:10.1002/mus.27038. Epub 2020 Aug 10.; Merkies IS, Schmitz PI, Samijn JP, et al. Fatigue in immune-mediated polyneuropathies. European Inflammatory Neuropathy Cause and Treatment (INCAT) Group. Neurology. 1999;53(8):1648-54. doi:10.1212/WNL.53.8.1648; Li SH, Lloyd AR, Graham BM. Physical and mental fatigue across the menstrual cycle in women with and without generalized anxiety disorder. Horm Behav. 2020 Feb;118:104667. doi:10.1016/j.yhbeh.2019.104667. Epub 2020 Jan 8.; Garssen MP, Bussmann JB, Schmitz PI, et al. Physical training and fatigue, fitness, and quality of life in Guillain-Barrе syndrome and CIDP. Neurology. 2004 Dec 28;63(12):2393-5. doi:10.1212/01.wnl.0000148589.87107.9c; Markvardsen LK, Carstens A-KR, Knak KL, et al. Muscle Strenght and Aerobic Capacity in Patients with CIDP One Year after Participation in an Exercise Trial. J Neuromuscular Dis. 2019;6(1):93-7. doi:10.3233/JND-180344

  9. 9
    Academic Journal

    Source: Neurology, Neuropsychiatry, Psychosomatics; Vol 13, No 5 (2021); 116-122 ; Неврология, нейропсихиатрия, психосоматика; Vol 13, No 5 (2021); 116-122 ; 2310-1342 ; 2074-2711 ; 10.14412/2074-2711-2021-5

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    Relation: https://nnp.ima-press.net/nnp/article/view/1675/1320; Шестакова МВ, Викулова ОК, Железнякова АВ и др. Эпидемиология сахарного диабета в Российской Федерации: что изменилось за последнее десятилетие? Терапевтический архив. 2019;91(10):4-13. doi:10.26442/00403660.2019.10.000364; Дедов ИИ, Шестакова МВ, Майоров АЮ и др. Сахарный диабет 2 типа у взрослых. Сахарный диабет. 2020;23(2S):4-102. doi:10.14341/DM12507; Cosentino F, Grant PJ, Aboyans V, et al. 2019 ESC Guidelines on diabetes, pre-diabetes, and cardiovascular diseases developed in collaboration with the EASD. Eur Heart J. 2020 Jan 7;41(2):255-323. doi:10.1093/eurheartj/ehz486; International Diabetes Federation. IDF Diabetes Atlas, 9 th ed. Brussels, Belgium: 2019. Available from: https://www.diabetesatlas.org; Pfannkuche A, Alhajjar A, Ming A, et al. Prevalence and risk factors of diabetic peripheral neuropathy in a diabetics cohort: Register initiative «diabetes and nerves». Endocr Metab Sci. 2020 Jul;1(1-2):100053. doi:10.1016/j.endmts.2020.100053; Stino AM, Smith AG. Peripheral neuropathy in prediabetes and the metabolic syndrome. J Diabetes Investig. 2017 Sep;8(5):646-55. doi:10.1111/jdi.12650; Kirthi V, Perumbalath A, Brown E, et al. Prevalence of peripheral neuropathy in pre-diabetes: a systematic review. BMJ Open Diabetes Res Care. 2021 May;9(1):e002040. doi:10.1136/bmjdrc-2020-002040; American Diabetes Association. Classification and Diagnosis of Diabetes: Standards of Medical Care in Diabetes – 2021. Diabetes Care. 2021 Jan;44(Suppl. 1):S15-S33. doi:10.2337/dc21-S002; Barrell K, Smith AG. Peripheral Neuropathy. Med Clin North Am. 2019 Mar;103(2):383-97. doi:10.1016/j.mcna.2018.10.006; Ziegler D, Rathmann W, Dickhaus T, et al. Prevalence of polyneuropathy in pre-diabetes and diabetes is associated with abdominal obesity and macroangiopathy: the MONICA/KORA Augsburg Surveys S2 and S3. Diabetes Care. 2008 Mar;31(3):464-9. doi:10.2337/dc07-1796; Kazamel M, Stino AM, Smith AG. Metabolic syndrome and peripheral neuropathy. Muscle Nerve. 2021 Mar;63(3):285-93. doi:10.1002/mus.27086; Ziegler D, Rathmann W, Dickhaus T, et al. Neuropathic pain in diabetes, prediabetes and normal glucose tolerance: the MONICA/KORA Augsburg Surveys S2 and S3. Pain Med. 2009 Mar;10(2):393-400. doi:10.1111/j.1526-4637.2008.00555.x; Lee CC, Perkins BA, Kayaniyil S, et al. Peripheral Neuropathy and Nerve Dysfunction in Individuals at High Risk for Type 2 Diabetes: The PROMISE Cohort. Diabetes Care. 2015 May;38(5):793-800. doi:10.2337/dc14-2585; Spallone V. Update on the Impact, Diagnosis and Management of Cardiovascular Autonomic Neuropathy in Diabetes: What Is Defined, What Is New, and What Is Unmet. Diabetes Metab J. 2019 Feb;43(1):3-30. doi:10.4093/dmj.2018.0259; Ziegler D, Voss A, Rathmann W, et al. Increased prevalence of cardiac autonomic dysfunction at different degrees of glucose intolerance in the general population: the KORA S4 survey. Diabetologia. 2015 May;58(5):1118-28. doi:10.1007/s00125-015-3534-7; Pop-Busui R, Boulton AJM, Feldman EL, et al. Diabetic neuropathy: a position statement by the American Diabetes Association. Diabetes Care. 2017;40:136-54. doi:10.2337/dc16-2042; Дедов ИИ, Шестакова МВ, Майоров АЮ, редакторы. Алгоритмы специализированной медицинской помощи больным сахарным диабетом: Клинические рекомендации. 9-й выпуск. Сахарный диабет. 2019;22(1S1):1-144. doi:10.14341/DM221S1; American Diabetes Association. Microvascular complications and foot care: Standards of Medical Care in Diabetes – 2021. Diabetes Care. 2021 Jan;44(Suppl. 1):S151-S167. doi:10.2337/dc21-S011; Papanas N, Ziegler D. Prediabetic neuropathy: does it exist? Curr Diab Rep. 2012 Aug;12(4):376-83. doi:10.1007/s11892-012-0278-3; Zeng J, Xu Y, Shi Y, Jiang C. Inflammation role in sensory neuropathy in Chinese patients with diabetes/prediabetes. Clin Neurol Neurosurg. 2018 Mar;166:136-40. doi:10.1016/j.clineuro.2018.01.031; Van der Velde JHPM, Koster A, Strotmeyer ES, et al. Cardiometabolic risk factors as determinants of peripheral nerve function: the Maastricht Study. Diabetologia. 2020 Aug;63(8):1648-58. doi:10.1007/s00125-020-05194-5; Kopf S, Groener JB, Kender Z, et al. Deep phenotyping neuropathy: An underestimated complication in patients with pre-diabetes and type 2 diabetes associated with albuminuria. Diabetes Res Clin Pract. 2018 Dec;146:191-201. doi:10.1016/j.diabres.2018.10.020; Thaisetthawatkul P, Fernandes Filho JA, Herrmann DN. Contribution of QSART to the diagnosis of small fiber neuropathy. Muscle Nerve. 2013 Dec;48(6):883-8. doi:10.1002/mus.23891; McArthur JC. Painful small fiber neuropathies. Continuum (Minneap Minn). 2012 Feb;18(1):106-25. doi:10.1212/01.CON.0000411570.79827.25; Divisova S, Vlckova E, Hnojcikova M, et al. Prediabetes/early diabetes-associated neuropathy predominantly involves sensory small fibres. J Peripher Nerv Syst. 2012 Sep;17(3):341-50. doi:10.1111/j.1529-8027.2012.00420.x; Asghar O, Petropoulos IN, Alam U, et al. Corneal confocal microscopy detects neuropathy in subjects with impaired glucose tolerance. Diabetes Care. 2014 Sep;37(9):2643-6. doi:10.2337/dc14-0279; DelMonte DW, Kim T. Anatomy and physiology of the cornea. J Cataract Refract Surg. 2011 Mar;37(3):588-98. doi:10.1016/j.jcrs.2010.12.037; Jende JME, Kender Z, Mooshage C, et al. Diffusion Tensor Imaging of the Sciatic Nerve as a Surrogate Marker for Nerve Functionality of the Upper and Lower Limb in Patients With Diabetes and Prediabetes. Front Neurosci. 2021 Mar;15:642589. doi:10.3389/fnins.2021.642589; Suo M, Wang P, Zhang M. Role of Fyn-mediated NMDA receptor function in prediabetic neuropathy in mice. J Neurophysiol. 2016 Aug;116(2):448-55. doi:10.1152/jn.00229.2016; Hinder LM, O'Brien PD, Hayes JM, et al. Dietary reversal of neuropathy in a murine model of prediabetes and metabolic syndrome. Dis Model Mech. 2017 Jun;10(6):717-25. doi:10.1242/dmm.028530; Roncero-Ramos I, Alcala-Diaz JF, Rangel-Zuniga OA, et al. Prediabetes diagnosis criteria, type 2 diabetes risk and dietary modulation: The CORDIOPREV study. Clin Nutr. 2020 Feb;39(2):492-500. doi:10.1016/j.clnu.2019.02.027; Hemmingsen B, Gimenez-Perez G, Mauricio D, et al. Diet, physical activity or both for prevention or delay of type 2 diabetes mellitus and its associated complications in people at increased risk of developing type 2 diabetes mellitus. Cochrane Database Syst Rev. 2017 Dec 4;12(12):CD003054. doi:10.1002/14651858.CD003054.pub4; Gong Q, Zhang P, Wang J, et al. Morbidity and mortality after lifestyle intervention for people with impaired glucose tolerance: 30year results of the Da Qing Diabetes Prevention Outcome Study. Lancet Diabetes Endocrinol. 2019 Jun;7(6):452-61. doi:10.1016/S2213-8587(19)30093-2; Nathan DM, Barrett-Connor E, Crandall JP, et al. Long-term effects of lifestyle intervention or metformin on diabetes development and microvascular complications over 15-year follow-up: the Diabetes Prevention Program Outcomes Study. Lancet Diabetes Endocrinol. 2015;3(11):866-75. doi:10.1016/S2213-8587(15)00291-0; Smith AG, Russell J, Feldman EL, et al. Lifestyle intervention for pre-diabetic neuropathy. Diabetes Care. 2006 Jun;29(6):1294-9. doi:10.2337/dc06-0224; Groover AL, Ryals JM, Guilford BL, et al. Exercise-mediated improvements in painful neuropathy associated with prediabetes in mice. Pain. 2013 Dec;154(12):2658-67. doi:10.1016/j.pain.2013.07.052; Carnethon MR, Prineas RJ, Temprosa M, et al. The association among autonomic nervous system function, incident diabetes, and intervention arm in the Diabetes Prevention Program. Diabetes Care. 2006 Apr;29(4):914-9. doi:10.2337/diacare.29.04.06.dc05-1729; Madsen KS, Chi Y, Metzendorf MI, et al. Metformin for prevention or delay of type 2 diabetes mellitus and its associated complications in persons at increased risk for the development of type 2 diabetes mellitus. Cochrane Database Syst Rev. 2019 Dec;12(12):CD008558. doi:10.1002/14651858.CD008558.pub2; Moelands SV, Lucassen PL, Akkermans RP, et al. Alpha-glucosidase inhibitors for prevention or delay of type 2 diabetes mellitus and its associated complications in people at increased risk of developing type 2 diabetes mellitus. Cochrane Database Syst Rev. 2018 Dec;12(12):CD005061. doi:10.1002/14651858.CD005061.pub3; Hemmingsen B, Sonne DP, Metzendorf MI, Richter B. Dipeptidyl-peptidase (DPP)-4 inhibitors and glucagon-like peptide (GLP)-1 analogues for prevention or delay of type 2 diabetes mellitus and its associated complications in people at increased risk for the development of type 2 diabetes mellitus. Cochrane Database Syst Rev. 2017 May;5(5):CD012204. doi:10.1002/14651858.CD012204.pub2; Infante M, Leoni M, Caprio M, Fabbri A. Long-term metformin therapy and vitamin B12 deficiency: An association to bear in mind. World J Diabetes. 2021 Jul;12(7):916-31. doi:10.4239/wjd.v12.i7.916; Inzucchi SE, Docherty KF, Kњber L, et al. Dapagliflozin and the Incidence of Type 2 Diabetes in Patients With Heart Failure and Reduced Ejection Fraction: An Exploratory Analysis From DAPA-HF. Diabetes Care. 2021 Feb;44(2):586-94. doi:10.2337/dc20-1675; Gabriel R, Boukichou Abdelkader N, Acosta T, et al. Early prevention of diabetes microvascular complications in people with hyperglycaemia in Europe. ePREDICE randomized trial. Study protocol, recruitment and selected baseline data. PLoS One. 2020 Apr;15(4):e0231196. doi:10.1371/journal.pone.0231196; Feldman EL, Callaghan BC, Pop-Busui R, et al. Diabetic neuropathy. Nat Rev Dis Primers. 2019 Jun;5(1):41. doi:10.1038/s41572-019-0092-1; Singh R, Kishore L, Kaur N. Diabetic peripheral neuropathy: current perspective and future directions. Pharmacol Res. 2014 Feb;80:21-35. doi:10.1016/j.phrs.2013.12.005; Rahimlou M, Asadi M, Banaei Jahromi N, Mansoori A. Alpha-lipoic acid (ALA) supplementation effect on glycemic and inflammatory biomarkers: A Systematic Review and meta-analysis. Clin Nutr ESPEN. 2019 Aug;32:16-28. doi:10.1016/j.clnesp.2019.03.015; Han T, Bai J, Liu W, Hu Y. A systematic review and meta-analysis of α-lipoic acid in the treatment of diabetic peripheral neuropathy. Eur J Endocrinol. 2012 Oct;167(4):465-71. doi:10.1530/EJE-12-0555; Ziegler D, Low PA, Litchy WJ, et al. Efficacy and safety of antioxidant treatment with α-lipoic acid over 4 year in diabetic polyneuropathy: the NATHAN 1 trial. Diabetes Care. 2011 Sep;34(9):2054-60. doi:10.2337/dc11-0503; Gosselin LE, Chrapowitzky L, Rideout TC. Metabolic effects of α-lipoic acid supplementation in pre-diabetics: a randomized, placebo-controlled pilot study. Food Funct. 2019 Sep;10(9):5732-8. doi:10.1039/c9fo00390h; Haghighatdoost F, Hariri M. Does alpha-lipoic acid affect lipid profile? A meta-analysis and systematic review on randomized controlled trials. Eur J Pharmacol. 2019 Mar;847:1-10. doi:10.1016/j.ejphar.2019.01.001

  10. 10
    Academic Journal

    Source: Obstetrics, Gynecology and Reproduction; Vol 15, No 4 (2021); 404-414 ; Акушерство, Гинекология и Репродукция; Vol 15, No 4 (2021); 404-414 ; 2500-3194 ; 2313-7347

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    Relation: https://www.gynecology.su/jour/article/view/1069/933; Гри Ж.-К., Макацария А.Д., Бицадзе В.О. и др. Антифосфолипидный синдром и беременность. Акушерство и гинекология. 2018;(10):5-11. https://doi.org/10.18565/aig.2018.10.5-11.; Vila P., Hernandez M.C., Lopez-Fernandez M.F., Batlle J. Prevalence, follow-up and clinical significance of the anticardiolipin antibodies in normal subjects. Thromb Haemost. 1994;72(2):209-13.; Макацария А.Д., Бицадзе В.О., Хизроева Д.Х. и др. Патогенетическое значение антифосфолипидных антител. Практическая медицина. 2012;(5):9-21.; Fleetwood T., Cantello R., Comi C. Antiphospholipid syndrome and the neurologist: from pathogenesis to therapy. Front Neurol. 2018;9:1001.; Gris J.-Ch., Nobile B., Bouvier S. Neuropsychiatric presentations of antiphospholipid antibodies. Thrombs Res. 2015;135(Suppl 1):S56-9. https://doi.org/10.1016/S0049-3848(15)50445-3.; Katzav A., Pick C.G., Korczyn A.D. et al. Hyperactivity in a mouse model of the antiphospholipid syndrome. Lupus. 2001;10(7):496-9. https://doi.org/10.1191/096120301678416060.; Chapman J., Cohen-Armon M., Shoenfeld Y., Korczyn A.D. Antiphospholipid antibodies permeabilize and depolarize brain synaptoneurosomes. Lupus. 1999;8(2):127-33. https://doi.org/10.1191/096120399678847524.; Блинов Д.В. Современные представления о роли нарушения резистентности гематоэнцефалического барьера в патогенезе заболеваний ЦНС. Часть 1: строение и формирование гематоэнцефалического барьера. Эпилепсия и пароксизмальные состояния. 2013;5(3):65-75.; Блинов Д.В. Современные представления о роли нарушения резистентности гематоэнцефалического барьера в патогенезе заболеваний ЦНС. Часть 2: функции и механизмы повреждения гематоэнцефалического барьера. Эпилепсия и пароксизмальные состояния. 2014;6(1):70-84. https://doi.org/; Блинов Д.В. Пациенты с неврологическими расстройствами: обоснование необходимости фармакоэкономической оценки оптимизации затрат на ведение с использованием нейроспецифических белков в качестве маркеров повышения проницаемости гематоэнцефалического барьера. ФАРМАКОЭКОНОМИКА. Современная фармакоэкономика и фармакоэпидемиология. 2014;7(1):40-5.; Маджидова Ё.Н., Рахимбаева Г.С., Азизова Р.Б. Нейроиммунопатогенетические механизмы эпилепсии. Эпилепсия и пароксизмальные состояния. 2014;6(1):15-8.; Huseynova S., Mukhtarova S., Alasgarova S. AO-40. Acute brain injury of very low birthweight infants born to mothers with autoimmune disorders in pregnancy. Early Human Development. 2010;86:S16. https://doi.org/10.1016/j.earlhumdev.2010.09.048.; Frauenknecht K., Katzav A., Grimm C. et al. Neurological impairment in experimental antiphospholipid syndrome is associated with increased ligand binding to hippocampal and cortical serotonergic 5-HT1A receptors. Immunobiology. 2013;218(4):517-26. https://doi.org/10.1016/j.imbio.2012.06.011.; Yaremchuk O.Z., Posokhova K.A., Tokarskyi O.S. The influence of L-arginine on the level of synthesis of nitric oxide and the content of glial fibrillary acidic protein in brain during experimental antiphospholipid syndrome. Scientific Issue Ternopil Volodymyr Hnatiuk National Pedagogical University. Series: Biology. 2019;77(3):39-45. https://doi.org/10.25128/2078-2357.19.3.5.; Yaremchuk O., Soroka Yu., Kulitska M. et al. Neuroprotective effect of aminoguanidine in experimental obstetric antiphospholipid syndrome. Georgian Med News. 2020;(301):159-65.; Rajput P.S., Lyden P.D., Chen B. et al. Protease activated receptor-1 mediates cytotoxicity during ischemia using in vivo and in vitro models. Neuroscience. 2014;281;229-40. https://doi.org/10.1016/j.neuroscience.2014.09.038.; Cervera R., Boffa M.C., Khamashta M.A., Hughes G.R. The EuroPhospholipid project: epidemiology of the antiphospholipid syndrome in Europe. Lupus. 2009;18(10):889-93. https://doi.org/10.1177/0961203309106832.; Kenet G., Sadetzki S., Murad H. et al. Leiden and antiphopholipid antibodies are significant risk factors for ischemic stroke in children. Stroke. 2000;31(6):1283-8. https://doi.org/10.1161/01.str.31.6.1283.; Sciascia S., Sanna G., Khamashta M.A. et al. The estimated frequency of antiphospholipid antibodies in young adults with cerebrovascular events: a systematic review. Ann Rheumat Dis. 2015;74(11):2028-33. https://doi.org/10.1136/annrheumdis-2014-205663.; Калашникова Л.А. Неврология антифосфолипидного синдрома. Медицина. М.: Медицина, 2003. 256 с.; Khamashta M.A., Cervera R., Asherson R.A. et al. Association of antibodies against phospholipids with valvular heart disease in patients with systemic lupus erythematosus. 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    Contributors: Настоящее исследование выполнено в рамках фунамен-тальной научной темы N AAA-A19-119021190145-2 по фрагменту «РЕНЕССАНС»

    Source: Rheumatology Science and Practice; Vol 58, No 1 (2020); 106-111 ; Научно-практическая ревматология; Vol 58, No 1 (2020); 106-111 ; 1995-4492 ; 1995-4484

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    Source: Student science in the XXI century; № 1(12); 15-17 ; Студенческая наука XXI века; № 1(12); 15-17 ; ISSN: 2413-3825 ; 2413-3825

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