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  1. 1
    Academic Journal

    Contributors: Not specified, Отсутствует

    Source: Current Pediatrics; Том 22, № 5 (2023); 415-424 ; Вопросы современной педиатрии; Том 22, № 5 (2023); 415-424 ; 1682-5535 ; 1682-5527

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    Relation: https://vsp.spr-journal.ru/jour/article/view/3303/1323; https://vsp.spr-journal.ru/jour/article/view/3303/1334; Oji V, Tadini G, Akiyama M, et al. Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009. J Am Acad Dermatol. 2010;63(4):607–641. doi: https://doi.org/10.1016/j.jaad.2009.11.020; Richard G. Autosomal Recessive Congenital Ichthyosis. 2001 Jan 10 [Updated 2023 Apr 20]. In: GeneReviews® [Internet]. Adam MP, Mirzaa GM, Pagon RA, et al., eds. Seattle (WA): University of Washington, Seattle; 1993–2023. Available online: https://www.ncbi.nlm.nih.gov/books/NBK1420. Accessed on October 19, 2023.; Мурашкин Н.Н., Аветисян К.О., Иванов Р.А., Макарова C.Г. Врожденный ихтиоз: клинико-генетические характеристики заболевания // Вопросы современной педиатрии. — 2022. — Т. 21. — № 5. — С. 362–377. — doi: https://doi.org/10.15690/vsp.v21i5.2459; Sun Q, Burgren NM, Cheraghlou S, et al. The Genomic and Phenotypic Landscape of Ichthyosis: An Analysis of 1000 Kindreds. JAMA Dermatol. 2022;158(1):16–25. doi: https://doi.org/10.1001/jamadermatol.2021.4242; Ихтиоз у детей: клинические рекомендации. — Союз педиатров России; 2016. — С. 6.; Lee AY. Molecular Mechanism of Epidermal Barrier Dysfunction as Primary Abnormalities. Int J Mol Sci. 2020;21(4):1194. doi: https://doi.org/10.3390/ijms21041194; Malik K, He H, Huynh TN, et al. Ichthyosis molecular fingerprinting shows profound TH17 skewing and a unique barrier genomic signature. J Allergy Clin Immunol. 2019;143(2):604–618. doi: https://doi.org/10.1016/j.jaci.2018.03.021; Кондратенко И.В., Бологов А.А. Первичные иммунодефициты: учебное пособие. — М.: ИндексМед Медиа; 2020. — С. 31.; Czarnowicki T, He H, Leonard A, et al. The Major Orphan Forms of Ichthyosis Are Characterized by Systemic T-Cell Activation and Th-17/Tc-17/Th-22/Tc-22 Polarization in Blood. J Invest Dermatol. 2018;138(10):2157–2167. doi: https://doi.org/10.1016/j.jid.2018.03.1523; Paller AS, Renert-Yuval Y, Suprun M, et al. An IL-17-dominant immune profile is shared across the major orphan forms of ichthyosis. J Allergy Clin Immunol. 2017;139(1):152–165. doi: https://doi.org/10.1016/j.jaci.2016.07.019; Mazereeuw-Hautier J, Vahlquist A, Traupe H, et al. Management of congenital ichthyoses: European guidelines of care, part one. Br J Dermatol. 2019;180(2):272–281. doi: https://doi.org/10.1111/bjd.17203; Mazereeuw-Hautier J, Hernández-Martín A, O’Toole EA, et al. Management of congenital ichthyoses: European guidelines of care, part two. Br J Dermatol. 2019;180(3):484–495. doi: https://doi.org/10.1111/bjd.16882; Youssefian L, Vahidnezhad H, Saeidian AH, et al. Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families. Hum Mutat. 2019;40(3):288–298. doi: https://doi.org/10.1002/humu.23695; Sabat R, Wolk K, Loyal L, et al. T cell pathology in skin inflammation. Semin Immunopathol. 2019;41(3):359–377. doi: https://doi.org/10.1007/s00281-019-00742-7; Купцова Д.Г., Радыгина Т.В., Курбатова О.В. и др. Содержание субпопуляций CD4+T-клеток в прогнозе эффективности биологической терапии псориаза у детей // Медицинская иммунология. — 2023. — Т. 25. — № 5. — С. 1071–1078. — doi: https://doi.org/10.15789/1563-0625-COC-2704; Mansouri Y, Guttman-Yassky E. Immune Pathways in Atopic Dermatitis, and Definition of Biomarkers through Broad and Targeted Therapeutics. J Clin Med. 2015;4(5):858–873. doi: https://doi.org/10.3390/jcm4050858; Мурашкин Н.Н., Опрятин Л.А., Епишев Р.В. и др. Новая эра в лечении атопического дерматита: результаты длительного применения дупилумаба // Вопросы современной педиатрии. — 2021. — Т. 20. — № 5. — С. 390–395. — doi: https://doi.org/10.15690/vsp.v20i5.2312; Купцова Д.Г., Петричук С.В., Мурашкин Н.Н. и др. Ранние предикторы эффективности биологической терапии псориаза у детей // Аллергология и иммунология в педиатрии. 2023. — № 1. — С. 49–52. — doi: https://doi.org/10.53529/2500-11752023-1-49-52; Tausend W, Downing C, Tyring S. Systematic review of interleukin-12, interleukin-17, and interleukin-23 pathway inhibitors for the treatment of moderate-to-severe chronic plaque psoriasis: ustekinumab, briakinumab, tildrakizumab, guselkumab, secukinumab, ixekizumab, and brodalumab. J Cutan Med Surg. 2014;18(3):156–169. doi: https://doi.org/10.2310/7750.2013.13125; Menter A, Strober BE, Kaplan DH, et al. Joint AAD-NPF guidelines of care for the management and treatment of psoriasis with biologics. J Am Acad Dermatol. 2019;80(4):1029–1072. doi: https://doi.org/10.1016/j.jaad.2018.11.057; Wollenberg A, Thomsen SF, Lacour JP, et al. Targeting immunoglobulin E in atopic dermatitis: A review of the existing evidence. World Allergy Organ J. 2021;14(3):100519. doi: https://doi.org/10.1016/j.waojou.2021.100519; Agache I, Akdis CA, Akdis M, et al. EAACI Biologicals Guidelinesdupilumab for children and adults with moderate-to-severe atopic dermatitis. Allergy. 2021;76(4):988–1009. doi: https://doi.org/10.1111/all.14690; Bieber T. Interleukin-13: Targeting an underestimated cytokine in atopic dermatitis. Allergy. 2020;75(1):54–62. doi: https://doi.org/10.1111/all.13954; Ghoreschi K, Balato A, Enerbäck C, Sabat R. Therapeutics targeting the IL-23 and IL-17 pathway in psoriasis. Lancet. 2021;397(10275):754–766. doi: https://doi.org/10.1016/s0140-6736(21)00184-7; Briot A, Deraison C, Lacroix M, et al. Kallikrein 5 induces atopic dermatitis-like lesions through PAR2-mediated thymic stromal lymphopoietin expression in Netherton syndrome. J Exp Med. 2009;206(5):1135–1147. doi: https://doi.org/10.1084/jem.20082242; Reche PA, Soumelis V, Gorman DM, et al. Human thymic stromal lymphopoietin preferentially stimulates myeloid cells. J Immunol. 2001;167(1):336–343. doi: https://doi.org/10.4049/jimmunol.167.1.336; Fontao L, Laffitte E, Briot A, et al. Infliximab infusions for Netherton syndrome: sustained clinical improvement correlates with a reduction of thymic stromal lymphopoietin levels in the skin. J Invest Dermatol. 2011;131(9):1947–1950. doi: https://doi.org/10.1038/jid.2011.124; Кондратенко И.В., Бологов А.А. Первичные иммунодефициты: учебное пособие. — М.: ИндексМед Медиа; 2020. — С. 117–120.; Eränkö E, Ilander M, Tuomiranta M, et al. Immune cell phenotype and functional defects in Netherton syndrome. Orphanet J Rare Dis. 2018;13(1):213. doi: https://doi.org/10.1186/s13023-018-0956-6; Hannula-Jouppi K, Laasanen SL, Ilander M, et al. Intrafamily and Interfamilial Phenotype Variation and Immature Immunity in Patients With Netherton Syndrome and Finnish SPINK5 Founder Mutation. JAMA Dermatol. 2016;152(4):435–442. doi: https://doi.org/10.1001/jamadermatol.2015.5827; Paller AS. Profiling Immune Expression to Consider Repurposing Therapeutics for the Ichthyoses. J Invest Dermatol. 2019;139(3): 535–540. doi: https://doi.org/10.1016/j.jid.2018.08.027; Paller AS, Czarnowicki T, Renert-Yuval Y, et al. The spectrum of manifestations in desmoplakin gene (DSP) spectrin repeat 6 domain mutations: Immunophenotyping and response to ustekinumab. J Am Acad Dermatol. 2018;78(3):498–505.e2. doi: https://doi.org/10.1016/j.jaad.2017.10.026; Luchsinger I, Knöpfel N, Theiler M, et al. Secukinumab Therapy for Netherton Syndrome. JAMA Dermatol. 2020;156(8):907–911. doi: https://doi.org/10.1001/jamadermatol.2020.1019; Yogarajah J, Gouveia C, Iype J, et al. Efficacy and safety of secukinumab for the treatment of severe ABCA12 deficiencyrelated ichthyosis in a child. Skin Health Dis. 2021;1(2):e25. doi: https://doi.org/10.1002/ski2.25

  2. 2
    Academic Journal

    Contributors: Not declared, Отсутствует

    Source: Current Pediatrics; Том 22, № 5 (2023); 382-386 ; Вопросы современной педиатрии; Том 22, № 5 (2023); 382-386 ; 1682-5535 ; 1682-5527

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    Relation: https://vsp.spr-journal.ru/jour/article/view/3298/1318; Rauer L, Reiger M, Bhattacharyya M, et al. Skin microbiome and its association with host cofactors in determining atopic dermatitis severity. J Eur Acad Dermatol Venereol. 2023;37(4):772–782. doi: https://doi.org/10.1111/jdv.18776; Boguniewicz M, Alexis AF, Beck LA, et al. Expert Perspectives on Management of Moderate-to-Severe Atopic Dermatitis: A Multidisciplinary Consensus Addressing Current and Emerging Therapies. J Allergy Clin Immunol Pract. 2017;5(6):1519–1531. doi: https://doi.org/10.1016/j.jaip.2017.08.005; Taylor K, Swan DJ, Affleck A, et al. Translational Research Network in Dermatology and the U.K. Dermatology Clinical Trials Network. Treatment of moderate-to-severe atopic eczema in adults within the U.K.: results of a national survey of dermatologists. Br J Dermatol. 2017;176(6):1617–1623. doi: https://doi.org/10.1111/bjd.15235; Silverberg JI, Barbarot S, Gadkari A, et al. Atopic dermatitis in the pediatric population: A cross-sectional, international epidemiologic study. Ann Allergy Asthma Immunol. 2021;126(4):417–428.e2. doi: https://doi.org/10.1016/j.anai.2020.12.020; Esaki H, Brunner PM, Renert-Yuval Y, et al. Early-onset pediatric atopic dermatitis is TH2 but also TH17 polarized in skin. J Allergy Clin Immunol. 2016;138(6):1639–1651. doi: https://doi.org/10.1016/j.jaci.2016.07.013; Lee HH, Patel KR, Singam V, et al. A systematic review and meta-analysis of the prevalence and phenotype of adult-onset atopic dermatitis. J Am Acad Dermatol. 2019;80(6):1526–1532.e7. doi: https://doi.org/10.1016/j.jaad.2018.05.1241; Agache I, Akdis CA. Precision medicine and phenotypes, endotypes, genotypes, regiotypes, and theratypes of allergic diseases. J Clin Invest. 2019;129(4):1493–1503. doi: https://doi.org/10.1172/JCI124611; Langan SM, Irvine AD, Weidinger S. Atopic dermatitis. Lancet. 2020;396(10247):345–360. doi: https://doi.org/10.1016/s0140-6736(20)31286-1; Nomura T, Wu J, Kabashima K, Guttman-Yassky E. Endophenotypic Variations of Atopic Dermatitis by Age, Race, and Ethnicity. J Allergy Clin Immunol Pract. 2020;8(6):1840–1852. doi: https://doi.org/10.1016/j.jaip.2020.02.022; Beck LA, Cork MJ, Amagai M, et al. Type 2 Inflammation Contributes to Skin Barrier Dysfunction in Atopic Dermatitis. JID Innov. 2022;2(5):100131. doi: https://doi.org/10.1016/j.xjidi.2022.100131; Weidinger S, Novak N. Atopic dermatitis. Lancet. 2016;387(10023): 1109–1122. doi: https://doi.org/10.1016/S0140-6736(15)00149-X; Barker JN, Palmer CN, Zhao Y, et al. Null mutations in the filaggrin gene (FLG) determine major susceptibility to early-onset atopic dermatitis that persists into adulthood. J Invest Dermatol. 2007;127(3):564–567. doi: https://doi.org/10.1038/sj.jid.5700587; Saunders SP, Moran T, Floudas A, et al. Spontaneous atopic dermatitis is mediated by innate immunity, with the secondary lung inflammation of the atopic march requiring adaptive immunity. J Allergy Clin Immunol. 2016;137(2):482–491. doi: https://doi.org/10.1016/j.jaci.2015.06.045; Elias PM, Hatano Y, Williams ML. Basis for the barrier abnormality in atopic dermatitis: Outside-inside-outside pathogenic mechanisms. J Allergy Clin Immunol. 2008;121(6):1337–1343. doi: https://doi.org/10.1016/j.jaci.2008.01.022; Kim BE, Leung DYM. Significance of Skin Barrier Dysfunction in Atopic Dermatitis. Allergy Asthma Immunol Res. 2018;10(3): 207–215. doi: https://doi.org/10.4168/aair.2018.10.3.207; Egawa G, Kabashima K. Multifactorial skin barrier deficiency and atopic dermatitis: Essential topics to prevent the atopic march. J Allergy Clin Immunol. 2016;138:350–358.e1. doi: https://doi.org/10.1016/j.jaci.2016.06.002; Spergel JM, Paller AS. Atopic dermatitis and the atopic march. J Allergy Clin Immunol. 2003;112(6 Suppl):S118–S127. doi: https://doi.org/10.1016/j.jaci.2003.09.033; Czarnowicki T, Krueger JG, Guttman-Yassky E. Novel concepts of prevention and treatment of atopic dermatitis through barrier and immune manipulations with implications for the atopic march. J Allergy Clin Immunol. 2017;139(6):1723–1734. doi: https://doi.org/10.1016/j.jaci.2017.04.004; Grobe W, Bieber T, Novak N. Pathophysiology of atopic dermatitis. J Dtsch Dermatol Ges. 2019;17(4):433–440. doi: https://doi.org/10.1111/ddg.13819; Nakahara T, Kido-Nakahara M, Tsuji G, Furue M. Basics and recent advances in the pathophysiology of atopic dermatitis. J Dermatol. 2020; 48(2):130–139. doi: https://doi.org/10.1111/1346-8138.15664; Yang G, Seok JK, Kang HC, et al. Skin Barrier Abnormalities and Immune Dysfunction in Atopic Dermatitis. Int J Mol Sci. 2020; 21(8):2867. doi: https://doi.org/10.3390/ijms21082867; Halling-Overgaard AS, Kezic S, Jakasa I, et al. Skin absorption through atopic dermatitis skin: A systematic review. Br J Dermatol. 2017;177(1):84–106. doi: https://doi.org/10.1111/bjd.15065; Tsakok T, Woolf R, Smith CH, et al. Atopic dermatitis: The skin barrier and beyond. Br J Dermatol. 2019;180(3):464–474. doi: https://doi.org/10.1111/bjd.16934; Ishikawa J, Narita H, Kondo N, et al. Changes in the ceramide profile of atopic dermatitis patients. J Invest Dermatol. 2010;130(10): 2511–2514. doi: https://doi.org/10.1038/jid.2010.161; Agrawal R, Woodfolk JA. Skin barrier defects in atopic dermatitis. Curr Allergy Asthma Rep. 2014;14(5):433. doi: https://doi.org/10.1007/s11882-014-0433-9; Zaniboni MC, Samorano LP, Orfali RL, Aoki V. Skin barrier in atopic dermatitis: Beyond filaggrin. Bras Dermatol. 2016;91(4):472–478. doi: https://doi.org/10.1590/abd1806-4841.20164412; Pellerin L, Henry J, Hsu CY, et al. Defects of filaggrin-like proteins in both lesional and nonlesional atopic skin. J Allergy Clin Immunol. 2013; 131(4):1094–1102. doi: https://doi.org/10.1016/j.jaci.2012.12.1566; Мурашкин Н.Н., Иванов Р.А., Амбарчян Э.Т. и др. Филаггрин и атопический дерматит: клинико-патогенетические параллели и возможности терапевтической коррекции // Вопросы современной педиатрии. — 2021. — Т. 20. — № 5. — С. 435–440. — doi: https://doi.org/10.15690/vsp.v20i5.2320; Moosbrugger-Martinz V, Leprince C, Méchin M-C, et al. Revisiting the Roles of Filaggrin in Atopic Dermatitis. Int J Mol Sci. 2022;23(10):5318. doi: https://doi.org/10.3390/ijms23105318; On HR, Lee SE, Kim SE, et al. Filaggrin Mutation in Korean Patients with Atopic Dermatitis. Yonsei Med J. 2017;58(2): 395–400. doi: https://doi.org/10.3349/ymj.2017.58.2.395; Osawa R, Akiyama M, Shimizu H. Filaggrin gene defects and the risk of developing allergic disorders. Allergol Int. 2011;60(1):1–9. doi: https://doi.org/10.2332/allergolint.10-RAI-0270; Čepelak I, Dodig S, Pavić I. Filaggrin and atopic march. Biochem Med (Zagreb). 2019;29(2):020501. doi: https://doi.org/10.11613/BM.2019.020501; Brown SJ, McLean WH. One remarkable molecule: filaggrin. J Invest Dermatol. 2012;132(3 Pt 2):751–762. doi: https://doi.org/10.1038/jid.2011.393; Scott IR, Harding CR, Barrett JG. Histidine-rich protein of the keratohyalin granules. Source of the free amino acids, urocanic acid and pyrrolidone carboxylic acid in the stratum corneum. Biochim Biophys Acta. 1982;719(1):110–117. doi: https://doi.org/10.1016/0304-4165(82)90314-2; Hoste E, Kemperman P, Devos M, et al. Caspase-14 is required for filaggrin degradation to natural moisturizing factors in the skin. J Invest Dermatol. 2011;131(11):2233–2241. doi: https://doi.org/10.1038/jid.2011.153; Kamata Y, Taniguchi A, Yamamoto M, et al. Neutral cysteine protease bleomycin hydrolase is essential for the breakdown of deiminated filaggrin into amino acids. J Biol Chem. 2009;284(19):12829–12836. doi: https://doi.org/10.1074/jbc.M807908200; Круглова Л.С., Переверзина Н.О. Филаггрин: от истории открытия до применения модуляторов филаггрина в клинической практике (обзор литературы) // Медицинский алфавит. — 2021. — № 27. — С. 8–12. — doi: https://doi.org/10.33667/2078-5631-2021-27-8-12; Мурашкин Н.Н., Епишев Р.В., Иванов Р.А. и др. Инновации в терапевтической коррекции микробиома кожи при атопическом дерматите в детском возрасте // Вопросы современной педиатрии. — 2022. — Т. 21. — № 5. — С. 352–361. — doi: https://doi.org/10.15690/vsp.v21i5.2449; Kezic S, O’Regan GM, Yau N, et al. Levels of filaggrin degradation products are influenced by both filaggrin genotype and atopic dermatitis severity. Allergy. 2011;66(7):934–940. doi: https://doi.org/10.1111/j.1398-9995.2010.02540.x; Zeeuwen PL, Ederveen TH, Van Der Krieken DA, et al. Grampositive anaerobe cocci are underrepresented in the microbiome of filaggrin-deficient human skin. J Allergy Clin Immunol. 2017;139(4): 1368–1371. doi: https://doi.org/10.1016/j.jaci.2016.09.017; Emmert H, Baurecht H, Thielking F, et al. Stratum corneum lipidomics analysis reveals altered ceramide profile in atopic dermatitis patients across body sites with correlated changes in skin microbiome. Exp Dermatol. 2021;30(10):1398–1408. doi: https://doi.org/10.1111/exd.14185; Clausen ML, Agner T, Lilje B, et al. Association of Disease Severity With Skin Microbiome and Filaggrin Gene Mutations in Adult Atopic Dermatitis. JAMA Dermatol. 2018;154(3):293–300. doi: https://doi.org/10.1001/jamadermatol.2017.5440; Baurecht H, Ruhlemann MC, Rodriguez E, et al. Epidermal lipid composition, barrier integrity, and eczematous inflammation are associated with skin microbiome configuration. J Allergy Clin Immunol. 2018;141(1):1668–1676. doi: https://doi.org/10.1016/j.jaci.2018.01.019; Мурашкин Н.Н., Амбарчян Э.Т., Материкин А.И., Епишев Р.В. Роль нарушений эпидермального барьера при атопическом дерматите: современные концепции патогенеза заболевания // Вопросы современной педиатрии. — 2018. — Т. 17. — № 1. — С. 85–88. — doi: https://doi.org/10.15690/vsp.v17i1.1859; Feuillie C, Vitry P, McAleer MA, et al. Adhesion of Staphylococcus aureus to corneocytes from atopic dermatitis patients is controlled by natural moisturizing factor levels. mBio. 2018;9(4):e01184-18. doi: https://doi.org/10.1128/mBio.01184-18; Мурашкин Н.Н., Опрятин Л.А., Епишев Р.В. и др. Дефект филаггрина при атопическом дерматите: современные методы коррекции // Вопросы современной педиатрии. — 2022. — Т. 21. — № 5. — С. 347–351. — doi: https://doi.org/10.15690/vsp.v21i5.2452; Topical skin care compositions. Patent. Publication Number: WO 2018/198039 A1. Publication Date: 01.11.2018. International Application No: PCT/IB2018/052866. International Filing Date: 25.04.2018. Applicant: DR. REDDY’S LABORATORIES LIMITED.; Татаурщикова Н.С., Летяева О.И., Русанова А.С. Ведение пациентов с атопическим дерматитом в рутинной клинической практике // РМЖ. Медицинское обозрение. — 2022. — Т. 6. — № 2. — С. 72–78. — doi: https://doi.org/10.32364/2587-68212022-6-2-72-78; Аравийская Е.Р., Бакулев А.Л., Гаджигороева А.Г. и др. Практические вопросы применения эмолентов, содержащих модуляторы филаггрина, в ведении пациентов с атопическим дерматитом и ксерозом: резолюция Совета экспертов // Российский аллергологический журнал. — 2022. — Т. 19. — № 2. — С. 245–258. — doi: https://doi.org/10.36691/RJA1538

  3. 3
    Academic Journal

    Source: Meditsinskiy sovet = Medical Council; № 17 (2023); 172-178 ; Медицинский Совет; № 17 (2023); 172-178 ; 2658-5790 ; 2079-701X

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    Relation: https://www.med-sovet.pro/jour/article/view/7837/6958; Кубанов АА, Намазова-Баранова ЛС, Хаитов РМ, Ильина НИ, Алексеева ЕА, Амбарчян ЭТ и др. Атопический дерматит: клинические рекомендации. М.; 2021. 81 с. Режим доступа: https://cr.minzdrav.gov.ru/recomend/265_2.; Nutten S. Atopic dermatitis: global epidemiology and risk factors. Ann Nutr Metab. 2015;66(Suppl. 1):8–16. https://doi.org/10.1159/000370220.; Lewis-Jones S. Quality of life and childhood atopic dermatitis: the misery of living with childhood eczema. Int J Clin Pract. 2006;60(8):984–992. https://doi.org/10.1111/j.1742-1241.2006.01047.x.; Liang Y, Chang C, Lu Q. The Genetics and Epigenetics of Atopic DermatitisFilaggrin and Other Polymorphisms. Clin Rev Allergy Immunol. 2016;51(3):315–328. https://doi.org/10.1007/s12016-015-8508-5.; Birben E, Sackesen C, Turgutoğlu N, Kalayci O. The role of SPINK5 in asthma related physiological events in the airway epithelium. 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  4. 4
    Academic Journal

    Contributors: Not specified, Отсутствует

    Source: Current Pediatrics; Том 21, № 5 (2022); 378-382 ; Вопросы современной педиатрии; Том 21, № 5 (2022); 378-382 ; 1682-5535 ; 1682-5527

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  5. 5
    Academic Journal

    Contributors: Not specified., Не указан.

    Source: Current Pediatrics; Том 20, № 5 (2021); 435-440 ; Вопросы современной педиатрии; Том 20, № 5 (2021); 435-440 ; 1682-5535 ; 1682-5527

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  6. 6
    Academic Journal

    Contributors: The article has been funded by Pierre Fabre., Статья опубликована при поддержке компании «Пьер Фабр».

    Source: Current Pediatrics; Том 19, № 3 (2020); 235-243 ; Вопросы современной педиатрии; Том 19, № 3 (2020); 235-243 ; 1682-5535 ; 1682-5527

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  7. 7
    Academic Journal

    Contributors: The article has been supported by Pierre Fabre LLC, Статья опубликована при поддержке ООО «Пьер Фабр»

    Source: Current Pediatrics; Том 18, № 5 (2019); 386-392 ; Вопросы современной педиатрии; Том 18, № 5 (2019); 386-392 ; 1682-5535 ; 1682-5527

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  8. 8
    Academic Journal

    Contributors: The article has been supported by Pierre Fabre LLC., Статья опубликована при поддержке компании Pierre Fabre.

    Source: Pediatric pharmacology; Том 17, № 4 (2020); 334-339 ; Педиатрическая фармакология; Том 17, № 4 (2020); 334-339 ; 2500-3089 ; 1727-5776

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  9. 9
  10. 10
    Academic Journal

    Contributors: Zeldis-Pharma LLC, ООО ЗелдисФарма

    Source: Current Pediatrics; Том 17, № 1 (2018); 85-88 ; Вопросы современной педиатрии; Том 17, № 1 (2018); 85-88 ; 1682-5535 ; 1682-5527

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    Academic Journal

    Contributors: Zeldis-Pharma LLC, OOO «Зелдис-Фарма»

    Source: Current Pediatrics; Том 17, № 4 (2018); 341-345 ; Вопросы современной педиатрии; Том 17, № 4 (2018); 341-345 ; 1682-5535 ; 1682-5527

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    Academic Journal

    Source: Bulletin of Siberian Medicine; Том 17, № 2 (2018); 114-120 ; Бюллетень сибирской медицины; Том 17, № 2 (2018); 114-120 ; 1819-3684 ; 1682-0363 ; 10.20538/1682-0363-2018-17-2

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