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  1. 1
    Academic Journal

    Source: Siberian journal of oncology; Том 23, № 6 (2024); 176-184 ; Сибирский онкологический журнал; Том 23, № 6 (2024); 176-184 ; 2312-3168 ; 1814-4861

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    Relation: https://www.siboncoj.ru/jour/article/view/3349/1294; Bray F., Laversanne M., Sung H., Ferlay J., Siegel R.L., Soerjomataram I., Jemal A. Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2024; 74(3): 229–63. doi:10.3322/caac.21834.; Состояние онкологической помощи населению России в 2022 году. Под ред. А.Д. Каприна, В.В. Старинского, А.О. Шахзадовой. М., 2023. 252 с.; Douillard J.Y., Rosell R., De Lena M., Carpagnano F., Ramlau R., Gonzáles-Larriba J.L., Grodzki T., Pereira J.R., Le Groumellec A., Lorusso V., Clary C., Torres A.J., Dahabreh J., Souquet P.J., Astudillo J., Fournel P., Artal-Cortes A., Jassem J., Koubkova L., His P., Riggi M., Hurteloup P. Adjuvant vinorelbine plus cisplatin versus observation in patients with completely resected stage IB-IIIA non-small-cell lung cancer (Adjuvant Navelbine International Trialist Association [ANITA]): a randomized controlled trial. Lancet Oncol. 2006; 7(9): 719–27. doi:10.1016/S1470-2045(06)70804-X. Erratum in: Lancet Oncol. 2006; 7(10): 797.; McMurry T.L., Stukenborg G.J., Kessler L.G., Colditz G.A., Wong M.L., Francescatti A.B., Jones D.R., Schumacher J.R., Greenberg C.C., Chang G.J., Winchester D.P., McKellar D.P., Kozower B.D. More Frequent Surveillance Following Lung Cancer Resection Is Not Associated With Improved Survival: A Nationally Representative Cohort Study. Ann Surg. 2018; 268(4): 632–39. doi:10.1097/SLA.0000000000002955.; Boyd J.A., Hubbs J.L., Kim D.W., Hollis D., Marks L.B., Kelsey C.R. Timing of local and distant failure in resected lung cancer: implications for reported rates of local failure. J Thorac Oncol. 2010; 5(2): 211–14. doi:10.1097/JTO.0b013e3181c20080.; Choi P.J., Jeong S.S., Yoon S.S. Prediction and prognostic factors of post-recurrence survival in recurred patients with early-stage NSCLC who underwent complete resection. J Thorac Dis. 2016; 8(1): 152–60. doi:10.3978/j.issn.2072-1439.2016.01.10.; Sekihara K., Hishida T., Yoshida J., Oki T., Omori T., Katsumata S., Ueda T., Miyoshi T., Goto M., Nakasone S., Ichikawa T., Matsuzawa R., Aokage K., Goto K., Tsuboi M. Long-term survival outcome after postoperative recurrence of non-small-cell lung cancer: who is ‘cured’ from postoperative recurrence? Eur J Cardiothorac Surg. 2017; 52(3): 522–28. doi:10.1093/ejcts/ezx127.; Tan W.L., Jain A., Takano A., Newell E.W., Iyer N.G., Lim W.T., Tan E.H., Zhai W., Hillmer A.M., Tam W.L., Tan D.S.W. Novel therapeutic targets on the horizon for lung cancer. Lancet Oncol. 2016; 17(8): 347–62. doi:10.1016/S1470-2045(16)30123-1.; Bai R., Lv Z., Xu D., Cui J. Predictive biomarkers for cancer immunotherapy with immune checkpoint inhibitors. Biomark Res. 2020; 8: 34. doi:10.1186/s40364-020-00209-0.; Antonia S., Goldberg S.B., Balmanoukian A., Chaft J.E., Sanborn R.E., Gupta A., Narwal R., Steele K., Gu Y., Karakunnel J.J., Rizvi N.A. Safety and antitumour activity of durvalumab plus tremelimumab in non-small cell lung cancer: a multicentre, phase 1b study. Lancet Oncol. 2016; 17(3): 299–308. doi:10.1016/S1470-2045(15)00544-6.; Rizvi N.A., Cho B.C., Reinmuth N., Lee K.H., Luft A., Ahn M.J., van den Heuvel M.M., Cobo M., Vicente D., Smolin A., Moiseyenko V., Antonia S.J., Le Moulec S., Robinet G., Natale R., Schneider J., Shepherd F.A., Geater S.L., Garon E.B., Kim E.S., Goldberg S.B., Nakagawa K., Raja R., Higgs B.W., Boothman A.M., Zhao L., Scheuring U., Stockman P.K., Chand V.K., Peters S.; MYSTIC Investigators. Durvalumab With or Without Tremelimumab vs Standard Chemotherapy in First-line Treatment of Metastatic Non-Small Cell Lung Cancer: The MYSTIC Phase 3 Randomized Clinical Trial. JAMA Oncol. 2020; 6(5): 661–74. doi:10.1001/jamaoncol.2020.0237. Erratum in: JAMA Oncol. 2020; 6(11): 1815.; Si H., Kuziora M., Quinn K.J., Helman E., Ye J., Liu F., Scheuring U., Peters S., Rizvi N.A., Brohawn P.Z., Ranade K., Higgs B.W., Banks K.C., Chand V.K., Raja R. A Blood-based Assay for Assessment of Tumor Mutational Burden in First-line Metastatic NSCLC Treatment: Results from the MYSTIC Study. Clin Cancer Res. 2021; 27(6): 1631–40. doi:10.1158/1078-0432.CCR-20-3771.; Phase III Open Label First Line Therapy Study of MEDI 4736 (Durvalumab) With or Without Tremelimumab Versus SOC in Non Small-Cell Lung Cancer (NSCLC) (MYSTIC) [Internet]. Clinical Trials.gov. URL: https://clinicaltrials.gov/study/NCT02453282 [cited 10.09.2024].; Моисеенко Ф.В., Волков Н.М., Абдулоева Н.Х., Левченко Н.В., Чубенко В.А., Жабина А.С., Чернобривцева В.В., Шугинова Т.Н., Шелехова К.В., Хенштейн В.А., Степанова М.Л., Крамчанинов М.М., Белухин С.А., Хабичева А.М., Артемьева Е.В., Носова М.В., Тулейко В.М., Моисеенко В.М. Результаты применения иммунотерапевтических препаратов при немелкоклеточном раке легкого в реальной клинической практике. Злокачественные опухоли. 2020; 10(1): 5–20. doi:10.18027/2224-5057-2020-10-1-5-20.; https://www.siboncoj.ru/jour/article/view/3349

  2. 2
    Academic Journal

    Source: PULMONOLOGIYA; Том 34, № 3 (2024); 401-408 ; Пульмонология; Том 34, № 3 (2024); 401-408 ; 2541-9617 ; 0869-0189

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    Relation: https://journal.pulmonology.ru/pulm/article/view/4562/3663; Ignarro L.J. Biosynthesis and metabolism of endothelium-derived nitric oxide. Ann. Rev. Pharmacol. Toxicol. 1990; 30: 535–560. DOI:10.1146/annurev.pa.30.040190.002535.; Knowles R.G., Moncada S. Nitric oxide synthases in mammals. Biochem. J. 1994; 298 (2): 249–258. DOI:10.1042/bj2980249.; Alderton W.K., Cooper C.E., Knowles R.G. Nitric oxide synthases: structure, function and inhibition. Biochem. J. 2001; 357 (Pt 3): 593–615. DOI:10.1042/bj3570593.; Korde Choudhari S., Chaudhary M., Bagde S. et al. Nitric oxide and cancer: a review. World J. Surg. Oncol. 2013; 11: 118. DOI:10.1186/1477-7819-11-118.; Lundberg J.O., Weitzberg E. Nitric oxide signaling in health and disease. Cell. 2022; 185 (16): 2853–2878. DOI:10.1016/j.cell.2022.06.010.; Yu B., Ichinose F., Bloch D.B., Zapol W.M. Inhaled nitric oxide. Br. J. Pharmacol. 2019; 176 (2): 246–255. DOI:10.1111/bph.14512.; Calabrese E.J., Baldwin L.A. Defining hormesis. Hum. Exp. Toxicol. 2002; 21 (2): 91–97. DOI:10.1191/0960327102ht217oa.; Ridnour L.A., Isenberg J.S., Espey M.G. et al. Nitric oxide regulates angiogenesis through a functional switch involving thrombospondin-1. Proc. Natl. Acad. Sci. 2005; 102 (37): 13147–13152. DOI:10.1073/pnas.0502979102.; Kashfi K. The dichotomous role of H2S in cancer cell biology? Déjà vu all over again. Biochem. Pharmacol. 2018; 149: 205–223. DOI:10.1016/j.bcp.2018.01.042.; Sessa W.C. eNOS at a glance. J. Cell Sci. 2004; 117 (Pt 12): 2427–2429. DOI:10.1242/jcs.01165.; Kleinert H., Schwarz P.M., Förstermann U. Regulation of the expression of inducible nitric oxide synthase. Biol. Chem. 2003; 384 (10-11): 1343–1364. DOI:10.1515/BC.2003.152.; Goligorsky M.S., Brodsky S.V., Noiri E. NO bioavailability, endothelial dysfunction, and acute renal failure: new insights into pathophysiology. Semin. Nephrol. 2004; 24 (4): 316–323. DOI:10.1016/j.semnephrol.2004.04.003.; Vannini F., Kashfi K., Nath N. The dual role of iNOS in cancer. Redox Biol. 2015; 6: 334–343. DOI:10.1016/j.redox.2015.08.009.; McGinity C.L., Palmieri E.M., Somasundaram V. et al. Nitric oxide modulates metabolic processes in the tumor immune microenvironment. Int. J. Mol. Sci. 2021; 22 (13): 7068. DOI:10.3390/ijms22137068.; Fukumura D., Kashiwagi S., Jain R.K. The role of nitric oxide in tumour progression. Nat. Rev. Cancer. 2006; 6 (7): 521–534. DOI:10.1038/nrc1910.; Hirst D., Robson T. Targeting nitric oxide for cancer therapy. J. Pharm. Pharmacol. 2010; 59 (1): 3–13. DOI:10.1211/jpp.59.1.0002.; Nguyen T., Brunson D., Crespi C.L. et al. DNA damage and mutation in human cells exposed to nitric oxide in vitro. Proc. Natl. Acad. Sci. USA. 1992; 89 (7): 3030–3034. DOI:10.1073/pnas.89.7.3030.; Yang Y.C., Chou H.Y.E., Shen T.L. et al. Topoisomerase II-mediated DNA cleavage and mutagenesis activated by nitric oxide underlie the inflammation-associated tumorigenesis. Antioxid. Redox Signal. 2013; 18 (10): 1129–1140. DOI:10.1089/ars.2012.4620.; Morbidelli L., Donnini S., Ziche M. Role of nitric oxide in the modulation of angiogenesis. Curr. Pharm. Des. 2003; 9 (7): 521–530. DOI:10.2174/1381612033391405.; Zhou J., Schmid T., Brüne B. HIF-1alpha and p53 as targets of NO in affecting cell proliferation, death and adaptation. Curr. Mol. Med. 2004; 4 (7): 741–751. DOI:10.2174/1566524043359926.; Thomas D.D., Espey M.G., Ridnour L.A. et al. Hypoxic inducible factor 1alpha, extracellular signal-regulated kinase, and p53 are regulated by distinct threshold concentrations of nitric oxide Hypoxic inducible factor 1α, extracellular signal-regulated kinase, and p53 are regulated by distinct threshold concentrations of nitric oxide. Proc. Natl. Acad. Sci. USA. 2004; 101 (24): 8894–8899. DOI:10.1073/pnas.0400453101.; Ha K.S., Kim K.M., Kwon Y.G. et al. Nitric oxide prevents 6‐hydroxydopamine‐induced apoptosis in PC12 cells through cGMP‐dependent PI3 kinase/Akt activation. FASEB J. 2003; 17 (9): 1036–1047. DOI:10.1096/fj.02-0738com.; Blaise G., Gauvin D., Gangal M., Authier S. Nitric oxide, cell signaling and cell death. Toxicology. 2005; 208 (2): 177–192. DOI:10.1016/j.tox.2004.11.032.; Maiuthed A., Bhummaphan N., Luanpitpong S. et al. Nitric oxide promotes cancer cell dedifferentiation by disrupting an Oct4:caveolin-1 complex: a new regulatory mechanism for cancer stem cell formation. J. Biol. Chem. 2018; 293 (35): 13534–13552. DOI:10.1074/jbc.RA117.000287.; Bonavida B., Baritaki S. Inhibition of epithelial-to-mesenchymal transition (EMT) in cancer by nitric oxide: pivotal roles of nitrosylation of NF-κB, YY1 and snail. For. Immunopathol. Dis. Ther. 2012; 3 (2): 125–133. DOI:10.1615/ForumImmunDisTher.2012006065.; Hickok J.R., Sahni S., Mikhed Y. et al. Nitric oxide suppresses tumor cell migration through N-Myc downstream-regulated Gene-1 (NDRG1) expression. J. Biol. Chem. 2011; 286 (48): 41413–41424. DOI:10.1074/jbc.M111.287052.; Vyas-Read S., Shaul P.W., Yuhanna I.S., Willis B.C. Nitric oxide attenuates epithelial-mesenchymal transition in alveolar epithelial cells. Am. J. Physiol. Lung Cell. Mol. Physiol. 2007; 293 (1): L212–221. DOI:10.1152/ajplung.00475.2006.; Wink D.A., Hines H.B., Cheng R.Y.S. et al. Nitric oxide and redox mechanisms in the immune response. J. Leukoc. Biol. 2011; 89 (6): 873–891. DOI:10.1189/jlb.1010550.; Huang Z., Fu J., Zhang Y. Nitric oxide donor-based cancer therapy: advances and prospects. J. Med. Chem. 2017; 60 (18): 7617–7635. DOI:10.1021/acs.jmedchem.6b01672.; Sorbo L.D., Michaelsen V.S., Ali A. et al. High doses of Inhaled nitric oxide as an innovative antimicrobial strategy for lung infections. Biomedicines. 2022; 10 (7): 1525. DOI:10.3390/biomedicines10071525.; Liu P.F., Zhao D.H., Qi Y. et al. The clinical value of exhaled nitric oxide in patients with lung cancer. Clin. Respir. J. 2018; 12 (1): 23–30. DOI:10.1111/crj.12471.; Li C.Y., Anuraga G., Chang C.P. et al. Repurposing nitric oxide donating drugs in cancer therapy through immune modulation. J. Exp. Clin. Cancer Res. 2023; 42 (1): 22. DOI:10.1186/s13046-022-02590-0.; Stevens E.V., Carpenter A.W., Shin J.H. et al. Nitric oxide-releasing silica nanoparticle inhibition of ovarian cancer cell growth. Mol. Pharm. 2010; 7 (3): 775–785. DOI:10.1021/mp9002865.; Munaweera I., Shi Y., Koneru B. et al. Nitric oxide- and cisplatin-releasing silica nanoparticles for use against non-small cell lung cancer. J. Inorg. Biochem. 2015; 153: 23–31. DOI:10.1016/j.jinorgbio.2015.09.002.; Thakkar S., Sharma D., Kalia K., Tekade R.K. Tumor microenvironment targeted nanotherapeutics for cancer therapy and diagnosis: a review. Acta Biomater. 2020; 101: 43–68. DOI:10.1016/j.actbio.2019.09.009.; Dong X., Liu H.J., Feng H.Y. et al. Enhanced drug delivery by nanoscale integration of a nitric oxide donor to induce tumor collagen depletion. Nano Lett. 2019; 19 (2): 997–1008. DOI:10.1021/acs.nanolett.8b04236.; Sung Y.C., Jin P.R., Chu L.A. et al. Delivery of nitric oxide with a nanocarrier promotes tumour vessel normalization and potentiates anti-cancer therapies. Nat. Nanotechnol. 2019; 14 (12): 1160–1169. DOI:10.1038/s41565-019-0570-3.; Jiang W., Dong W., Li M. et al. Nitric oxide induces immunogenic cell death and potentiates cancer immunotherapy. ACS Nano. 2022; 16 (3): 3881–3894. DOI:10.1021/acsnano.1c09048.; Levy E.S., Morales D.P., Garcia J.V. et al. Near-IR mediated intracellular uncaging of NO from cell targeted hollow gold nanoparticles. Chem. Commun. (Camb). 2015; 51 (100): 17692–17695. DOI:10.1039/C5CC07989F.; Wang L., Chang Y., Feng Y. et al. Nitric oxide stimulated programmable drug release of nanosystem for multidrug resistance cancer therapy. Nano Lett. 2019; 19 (10): 6800–6811. DOI:10.1021/acs.nanolett.9b01869.; Ishima Y., Fang J., Kragh-Hansen U. et al. Tuning of poly-S-nitrosated human serum albumin as superior antitumor nanomedicine. J. Pharm. Sci. 2014; 103 (7): 2184–2188. DOI:10.1002/jps.24020.; Heinecke J.L., Ridnour L.A., Cheng R.Y.S. et al. Tumor microenvironment-based feed-forward regulation of NOS2 in breast cancer progression. Proc. Natl. Acad. Sci. USA. 2014; 111 (17): 6323–6328. DOI:10.1073/pnas.1401799111.; Girotti A.W., Bazak J., Korytowski W. Pro-tumor activity of endogenous nitric oxide in anti-tumor photodynamic therapy: recently recognized bystander effects. Int. J. Mol. Sci. 2023; 24 (14): 11559. DOI:10.3390/ijms241411559.; Cheng R.Y.S., Ridnour L.A., Wink A.L. et al. Interferon-gamma is quintessential for NOS2 and COX2 expression in ER- breast tumors that lead to poor outcome. Cell Death Dis. 2023; 14 (5): 319. DOI:10.1038/s41419-023-05834-9.; Basudhar D., Glynn S.A., Greer M. et al. Coexpression of NOS2 and COX2 accelerates tumor growth and reduces survival in estrogen receptor-negative breast cancer. Proc. Natl. Acad. Sci. USA. 2017; 114 (49): 13030–13035. DOI:10.1073/pnas.1709119114.; Dávila-González D., Choi D.S., Rosato R.R. et al. Pharmacological inhibition of NOS activates ASK1/JNK pathway augmenting docetaxel-mediated apoptosis in triple-negative breast cancer. Clin. Cancer Res. 2018; 24 (5): 1152–1162. DOI:10.1158/1078-0432.CCR-17-1437.; Pershing N.L.K., Yang C.F.J., Xu M., Counter C.M. Treatment with the nitric oxide synthase inhibitor L-NAME provides a survival advantage in a mouse model of Kras mutation-positive, non-small cell lung cancer. Oncotarget. 2106; 7 (27): 42385–42392. DOI:10.18632/oncotarget.9874.; https://journal.pulmonology.ru/pulm/article/view/4562

  3. 3
    Academic Journal

    Source: Neurology, Neuropsychiatry, Psychosomatics; Vol 16, No 2 (2024); 34-40 ; Неврология, нейропсихиатрия, психосоматика; Vol 16, No 2 (2024); 34-40 ; 2310-1342 ; 2074-2711 ; 10.14412/2074-2711-2024-2

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    Relation: https://nnp.ima-press.net/nnp/article/view/2222/1647; Литвиненко ИВ, Одинак ММ. Рациональный подход к медикаментозной терапии – основа обеспечения качества жизни при болезни Паркинсона. Военно-медицинский журнал. 2004;325(4):47-53.; Гусев ЕИ, Коновалов АН, Скворцова ВИ, Гехт АБ, редакторы. Неврология: Национальное руководство. Москва: ГЭОТАР-Медиа; 2009. 1035 с.; Armstrong MJ, Okun MS. Diagnosis and Treatment of Parkinson Disease: A Review. JAMA. 2020 Feb 11;323(6):548-60. doi:10.1001/jama.2019.22360; Madelein van der Stouwe AM, Nieuwhof F, Helmich RC. Tremor pathophysiology: lessons from neuroimaging. Curr Opin Neurol. 2020 Aug;33(4):474-81. doi:10.1097/WCO.0000000000000829; Timmer J, Lauk M, Vach W, et al. A test for a difference between spectral peak frequencies. Comp Stat Data Anal. 1999;30:45-55.; Raethjen J, Govindan RB, Muthuraman M, et al. Cortical correlates of the basic and first harmonic frequency of Parkinsonian tremor. Clin Neurophysiol. 2009 Oct;120(10):1866-72. doi:10.1016/j.clinph.2009.06.028. Epub 2009 Sep 12.; Pollok B, Makhloufi H, Butz M, et al. Levodopa affects functional brain networks in Parkinsonian resting tremor. Mov Disord. 2009 Jan 15;24(1):91-8. doi:10.1002/mds.22318; Dirkx MF, Bologna M. The pathophysiology of Parkinson's disease tremor. J Neurol Sci. 2022 Apr 15;435:120196. doi:10.1016/j.jns.2022.120196. Epub 2022 Feb 19.; Голубев ВЛ. Диагностика и терапия дрожательной формы болезни Паркинсона. В кн.: Иллариошкин СН, Яхно НН, редакторы. Болезнь Паркинсона и расстройства движений. Москва: Диалог; 2008. С. 85-8.; Yaw TK, Fox SH, Lang AE. Clozapine in Parkinsonian Rest Tremor: A Review of Outcomes, Adverse Reactions, and Possible Mechanisms of Action. Mov Disord Clin Pract. 2015 Dec 30;3(2):116-24. doi:10.1002/mdc3.12266; Нодель МР. Современные диагностические критерии болезни Паркинсона. Российский журнал гериатрической медицины. 2021;(1):92-6. doi:10.37586/2686-8636-1-2021-92-96; Протокол ведения больных. Болезнь Паркинсона (G20) [утвержден Минздравсоцразвития РФ 14.01.2005]. Проблемы стандартизации в здравоохранении. 2005;(3):74-166.; Berardelli A, Wenning GK, Antonini A, et al. EFNS/MDS-ES/ENS [corrected] recommendations for the diagnosis of Parkinson's disease. Eur J Neurol. 2013 Jan;20(1):16-34. doi:10.1111/ene.12022. Erratum in: Eur J Neurol. 2013 Feb;20(2):406.; Федорова НВ, Шток ВН. Стратегия и тактика лечения болезни Паркинсона. Консилиум. 2001;(5):237-42.; Преображенская ИС, Яхно НН. Лечение болезни Паркинсона. Consilium Medicum. 2002;4(2):85–91.; Карабань ИН и др. Болезнь Паркинсона (G20): Клинические рекомендации. Новости медицины и фармации: Психиатрия и неврология. 2007;215. Доступно по ссылке: http://www.mif-ua.com/archive/article/1396 (дата обращения 19.02.2014).; Левин ОС. Стандарты лечения болезни Паркинсона. Лечащий врач. 2007;8/9. 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    Source: Almanac of Clinical Medicine; Vol 50, No 1 (2022); 47-55 ; Альманах клинической медицины; Vol 50, No 1 (2022); 47-55 ; 2587-9294 ; 2072-0505

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    Source: Siberian journal of oncology; Том 20, № 4 (2021); 116-121 ; Сибирский онкологический журнал; Том 20, № 4 (2021); 116-121 ; 2312-3168 ; 1814-4861 ; 10.21294/1814-4861-2021-20-4

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    Source: Siberian journal of oncology; Том 20, № 2 (2021); 118-126 ; Сибирский онкологический журнал; Том 20, № 2 (2021); 118-126 ; 2312-3168 ; 1814-4861 ; 10.21294/1814-4861-2021-20-2

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  17. 17
    Academic Journal

    Contributors: Исследование проводилось в рамках выполнения научной темы № 398 «Патогенетические особенности и персонифицированная терапия анкилозирующего спондилита и псориатического артрита», утвержденной Ученым советом ФГБНУ НИИР им. В.А. Насоновой. Авторы несут полную ответственность за предоставление окончательной версии рукописи в печать.

    Source: Rheumatology Science and Practice; Vol 59, No 3 (2021); 288-295 ; Научно-практическая ревматология; Vol 59, No 3 (2021); 288-295 ; 1995-4492 ; 1995-4484

    File Description: application/pdf

    Relation: https://rsp.mediar-press.net/rsp/article/view/3040/2094; Ушкалова ЕА, Ткачева ОН, Чухарева НА. Проблема безопасности применения лекарственных средств во время беременности и кормления грудью. Акушерство и гинекология. 2011;(2):4-7.; Гандалоева ЗМ, Кричевская ОА, Глухова СИ, Дубинина ТВ, Лила АМ, и др. Беременность при анкилозирующем спондилите: взгляд пациентки и врача. Современная ревматология. 2019;13(1):71-79. doi:10.14412/1996-7012-2019-1-71-79; Gotestam Skorpen C, Hoeltzenbein M, Tincani A, FischerBetz R, Elefant E, Chambers C, et al. The EULAR points to consider for use of antirheumatic drugs before pregnancy, and during pregnancy and lactation. Ann Rheum Dis. 2016;75(5):795810. doi:10.1136/annrheumdis-2015-208840; Кошелева НМ. Планирование беременности и наблюдение за беременными с ревматическими заболеваниями. В кн.: Насонов ЕЛ (ред.). Российские клинические рекомендации. Ревматология. М.:ГЭОТАР-Медиа;2017:380-389.; Tincani A, Taylor P, Fischer-Betz R, Ecoffet C, Chakravarty E. Fears and misconceptions of women with chronic rheumatic diseases on their journey to motherhood. Ann Rheum Dis. 2018;77(Suppl):A866. doi:10.1136/annrheumdis-2018-eular.2063; Haroun T, Eudy AM, Jayasundara M, Nowell WB, Curtis JR, White CW, et al. Tough choices: Understanding the medication decision-making process for women with inflammatory arthritis during pregnancy and lactation. ACR/ARHP Annual Meeting. San Diego, CA;2017 Nov 3-8, 2017:Abstract 1298.; Smolen JS, Gladman D, McNeil HP, Mease PJ, Sieper J, Hojnik M, et al. Predicting adherence to therapy in rheumatoid arthritis, psoriatic arthritis or ankylosing spondylitis: A large crosssectional study. RMD Open 2019;5:e000585. doi:10.1136/rmdopen-2017-000585; Michetti P, Weinman J, Mrowietz U, Smolen J, Peyrin-Biroulet L, Louis E, et al. Impact of treatment-related beliefs on medication adherence in immune-mediated inflammatory diseases: Results of the global ALIGN study. Adv Ther. 2017;34(1):91-108. doi:10.1007/s12325-016-0441-3; van den Brandt S, Zbinden A, Baeten D, Villiger PM, Østensen M, Förger F. Risk factors for flare and treatment of disease flares during pregnancy in rheumatoid arthritis and axial spondyloarthritis patients. Arthritis Res Ther. 2017;19(1):64. doi:10.1186/s13075-017-1269-1; Genest G, Spitzer KA, Laskin CA. Maternal and fetal outcomes in a cohort of patients exposed to tumor necrosis factor inhibitors throughout pregnancy. J Rheumatol. 2018;45(8):1109-1115. doi:10.3899/jrheum.171152; Sieper J, Rudwaleit M, Baraliakos X, Brandt J, Braun J, BurgosVargas R, et al. The Assessment of SpondyloArthritis international Society (ASAS) handbook: A guide to assess spondyloarthritis. Ann Rheum Dis. 2009;68(2):ii1-ii44. doi:10.1136/ard.2008.104018; Dougados M. ASAS recommendations for collecting, analysing and reporting NSAID intake in clinical trials/epidemiological studies in axial spondyloarthritis. Ann Rheum Dis. 2011;70:249-251. doi:10.1136/ard.2010.133488; Shalansky SJ, Levy AR, Ignaszewski AP. Self-reported Morisky score for identifying nonadherence with cardiovascular medications. Ann Pharmacother. 2004;38:1363-1368.; Ostensen M, Husby G. A prospective clinical study of the effect of pregnancy on rheumatoid arthritis and ankylosing spondylitis. Arthritis Rheum. 1983;26(9):1155-1159.; Timur H, Tokmak A, Turkmen GG, Ali İnal H, Uygur D, Danışman N. Pregnancy outcome in patients with ankylosing spondylitis. J Matern Fetal Neonatal Med. 2016;29(15):2470-2474. doi:10.3109/14767058.2015.1089432; Ursin K, Lydersen S, Skomsvoll JF, Wallenius M. Disease activity during and after pregnancy in women with axial spondyloarthritis: A prospective multicentre study. Rheumatology (Oxford). 2018;57(6):1064-1071. doi:10.1093/rheumatology/key047; Zbinden A, van den Brandt S, Ostensen M, Villiger PM, Förger F. Risk for adverse pregnancy outcome in axial spondyloarthritis and rheumatoid arthritis: Disease activity matters. Rheumatology. 2018;57:1235-1242. doi:10.1093/rheumatology/key053; Smith CJF, Bandoli G, Kavanaugh A, Chambers CD. Birth outcomes and disease activity during pregnancy in a prospective cohort of women with psoriaric arthritis and ankylosing spondylitis. Arthritis Care Res (Hoboken). 2020;72(7):1029-1037. doi:10.1002/acr.23924; Кричевская ОА, Гандалоева ЗМ, Дубинина ТВ. Анкилозирующий спондилит и беременность: Современный взгляд на проблему. Современная ревматология. 2018;12(3):19-28. doi:10.14412/1996-7012-2018-3-19-28

  18. 18
    Academic Journal

    Contributors: The publication of the article is supported by Bayer, JSC, Публикация статьи поддержана компанией АО «БАЙЕР»

    Source: Rational Pharmacotherapy in Cardiology; Vol 17, No 2 (2021); 278-285 ; Рациональная Фармакотерапия в Кардиологии; Vol 17, No 2 (2021); 278-285 ; 2225-3653 ; 1819-6446

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Imaging findings in pulmonary vasculitis. Semin Ultrasound CT MR. 2012;33:567-79. DOI:10.1053/j.sult.2012.05.001.; Nawaz A, Litt HI, Stavropoulos SW, et al. Digital subtraction pulmonary arteriography versus multidetector CT in the detection of pulmonary arteriovenous malformations. J Vasc Interv Radiol. 2008;19:1582-8. DOI:10.1016/j.jvir.2008.07.011.; Madani MM. Surgical treatment of chronic thromboembolic pulmonary hypertension: pulmonary thromboendarterectomy. Methodist Debakey Cardiovasc J. 2016;12(4):213-8. DOI:10.14797/mdcj-12-4-213.; Mizoguchi H, Ogawa A, Munemasa M, et al. Refined Balloon Pulmonary Angioplasty for Inoperable Patients with Chronic Thromboembolic Pulmonary Hypertension. Circ Cardiovasc Interv. 2012;5:748- 55. DOI:10.1161/CIRCINTERVENTIONS.112.971077.; Fukui S, Ogo T, Goto Y, et al. Exercise intolerance and ventilatory inefficiency improve early after balloon pulmonary angioplasty in patients with inoperable chronic thromboembolic pulmonary hypertension. 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    Source: Almanac of Clinical Medicine; Vol 49, No 7 (2021); 443-454 ; Альманах клинической медицины; Vol 49, No 7 (2021); 443-454 ; 2587-9294 ; 2072-0505

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