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  • Tag › genetic polymorphisms

     Clinical and genetic characteristics of lipid metabolism in infants born to mothers with gestational diabetes mellitus

    Редактор | 2026, Original articles, Practical medicine part 24 №3. 2026 | 5 июня, 2026

    K.S. LUGOVYKH1, S.YU. ZAKHAROVA1, L.A. PESTRYAEVA1, T.B. TRETYAKOVA1, 2, E.G. DERYABINA1, 2  ¹Ural Scientific Research Institute of Maternity and Child Care, Yekaterinburg 2Urals State Medical University, Yekaterinburg Contact details: Lugovykh K.S. — neonatologist of the Department of Pathology of Newborns and Premature Babies Address: 1 Repin St., 1620028 Yekaterinburg, Russian Federation, tel.: +7-908-906-68-78, е-mail: karina01.00@mail.ru Children born to […]

    Tag: 2026, E.G. DERYABINA, genetic polymorphisms, gestational diabetes mellitus, K.S. LUGOVYKH, L.A. PESTRYAEVA, lipid metabolism, lipid transport system, Newborn, Practical medicine part 24 №3. 2026, S.YU. ZAKHAROVA, T.B. TRETYAKOVA
    Комментарии к записи  Clinical and genetic characteristics of lipid metabolism in infants born to mothers with gestational diabetes mellitus отключены

     Genetic mechanisms of aspirin resistance in patients with atherothrombotic variant of ischemic stroke

    Редактор | 2022, Articles based on dissertstions, Practical medicine part 20 №5. 2022 | 11 октября, 2022

    T.E. EVERSTOVA1, T.YA. NIKOLAEVA2, S.A. CHUGUNOVA2  1Republic Hospital No. 2 — Center for Emergency Medical Aid, Yakutsk 2North-Eastern Federal University named after M.K. Ammosov, Yakutsk Contact details: Everstova T.E. — post-graduate student of the Department of Neurology and Psychiatry Address: 58 Belinsky St., Yakutsk, Russian Federation, 677000, tel.: +7-914-227-68-19, e-mail: selectir_66@mail.ru  The purpose — to […]

    Tag: 2022, aspirin, aspirin resistance, genetic polymorphisms, ischemic stroke, Practical medicine part 20 №5. 2022, S.A. CHUGUNOVA, T.E. EVERSTOVA, T.Ya. NIKOLAEVA
    Комментарии к записи  Genetic mechanisms of aspirin resistance in patients with atherothrombotic variant of ischemic stroke отключены

    VKORC1 CC genotype is associated with activation of the coagulation cascade and reduction of fibrinolytic activity in patients with atrial fibrillation.

    Редакция | 2015, PM Cardiology, Practical medicine 03 (15) Cardiology. Rheumatology. Part 2 | 26 мая, 2015

    A.O. RUBANENKO, YU.V. SCHUKIN Samara State Medical University, 89 Chapaevskaya St., Samara, Russian Federation, 443099 Rubanenko A.O. — Cand. of Med. Sc., Assistant of the Department of Propaedeutic Therapy, tel. +7-927-201-09-44, e-mail: anatolii.rubanenko@gmail.com Schukin Yu.V. — D. Med. Sc., Head of the Department of Propaedeutic Therapy, tel. +7-927-262-09-03, e-mail: samgmu_pt@mail.ru This article is related to […]

    Tag: A.O. RUBANENKO, atrial fibrillation, genetic polymorphisms, hemostasis, Practical medicine 03 (15) Cardiology. Rheumatology. Part 2, subunit 1 (VKORC1), thrombin-activatable fibrinolysis inhibitor (TAFI), vitamin К epoxide reductase complex, YU.V. SCHUKIN
    Комментарии к записи VKORC1 CC genotype is associated with activation of the coagulation cascade and reduction of fibrinolytic activity in patients with atrial fibrillation. отключены
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