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2019 14
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Management of antithrombin deficiency: an update for clinicians.
Bravo-Pérez C, Vicente V, Corral J. Bravo-Pérez C, et al. Expert Rev Hematol. 2019 Jun;12(6):397-405. doi: 10.1080/17474086.2019.1611424. Epub 2019 May 22. Expert Rev Hematol. 2019. PMID: 31116611 Review.
Antithrombin is a serpin that inhibits multiple procoagulant serine proteases and acts as an endogenous anticoagulant. Thus, congenital antithrombin deficiency constitutes a major thrombophilic state, the most severe so far. ...In the present work, we globally revie …
Antithrombin is a serpin that inhibits multiple procoagulant serine proteases and acts as an endogenous anticoagulant. Thus, congenital a …
Antithrombin Deficiency in Trauma and Surgical Critical Care.
Ehrhardt JD Jr, Boneva D, McKenney M, Elkbuli A. Ehrhardt JD Jr, et al. J Surg Res. 2020 Dec;256:536-542. doi: 10.1016/j.jss.2020.07.010. Epub 2020 Aug 13. J Surg Res. 2020. PMID: 32799002 Review.
Antithrombin deficiency (ATD) was described in 1965 by Olav Egeberg as the first known inherited form of thrombophilia. ...
Antithrombin deficiency (ATD) was described in 1965 by Olav Egeberg as the first known inherited form of thrombophilia. ...
Management of Antithrombin Deficiency in Pregnancy.
Hart C, Rott H, Heimerl S, Linnemann B. Hart C, et al. Hamostaseologie. 2022 Oct;42(5):320-329. doi: 10.1055/a-1841-0399. Epub 2022 Nov 2. Hamostaseologie. 2022. PMID: 36323279 Free article.
Gene editing of human iPSCs rescues thrombophilia in hereditary antithrombin deficiency in mice.
Tang LV, Tao Y, Feng Y, Ma J, Lin W, Zhang Y, Zhang Y, Wu T, Cai Y, Lu H, Wei J, Corral J, Hu Y. Tang LV, et al. Sci Transl Med. 2022 Nov 30;14(673):eabq3202. doi: 10.1126/scitranslmed.abq3202. Epub 2022 Nov 30. Sci Transl Med. 2022. PMID: 36449603
Hereditary antithrombin deficiency is caused by SERPINC1 gene mutations and predisposes to recurrent venous thromboembolism that can be life-threatening. ...In this study, peripheral blood mononuclear cells from a patient with severe antithrombin deficienc …
Hereditary antithrombin deficiency is caused by SERPINC1 gene mutations and predisposes to recurrent venous thromboembolism th …
Antithrombin deficiency: A pediatric disorder.
Smith N, Warren BB, Smith J, Jacobson L, Armstrong J, Kim J, Di Paola J, Manco-Johnson M. Smith N, et al. Thromb Res. 2021 Jun;202:45-51. doi: 10.1016/j.thromres.2021.02.029. Epub 2021 Mar 3. Thromb Res. 2021. PMID: 33725558
Management of antithrombin deficiency.
Pabinger-Fasching I. Pabinger-Fasching I. Clin Adv Hematol Oncol. 2023 May;21(5):232-234. Clin Adv Hematol Oncol. 2023. PMID: 37145492 No abstract available.
Molecular and clinical characterization of transient antithrombin deficiency: A new concept in congenital thrombophilia.
Bravo-Pérez C, de la Morena-Barrio ME, de la Morena-Barrio B, Miñano A, Padilla J, Cifuentes R, Garrido P, Vicente V, Corral J. Bravo-Pérez C, et al. Am J Hematol. 2022 Feb 1;97(2):216-225. doi: 10.1002/ajh.26413. Epub 2021 Nov 24. Am J Hematol. 2022. PMID: 34800304 Free article.
Antithrombin deficiency, the most severe thrombophilia, might be underestimated, since it is only investigated in cases with consistent functional deficiency or family history. ...Antithrombin deficiency is underestimated, and molecular screening might …
Antithrombin deficiency, the most severe thrombophilia, might be underestimated, since it is only investigated in cases with c …
Gene editing addresses antithrombin deficiency.
Crunkhorn S. Crunkhorn S. Nat Rev Drug Discov. 2023 Feb;22(2):99. doi: 10.1038/d41573-023-00008-w. Nat Rev Drug Discov. 2023. PMID: 36631697 No abstract available.
67 results