Similar articles for PMID: 24196373

Year	Number of Results
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1

Impact of the type of SERPINC1 mutation and subtype of antithrombin deficiency on the thrombotic phenotype in hereditary antithrombin deficiency.

Luxembourg B, Pavlova A, Geisen C, Spannagl M, Bergmann F, Krause M, Alesci S, Seifried E, Lindhoff-Last E. Luxembourg B, et al. Thromb Haemost. 2014 Feb;111(2):249-57. doi: 10.1160/TH13-05-0402. Epub 2013 Nov 7. Thromb Haemost. 2014. PMID: 24196373

2

Thrombotic risk according to SERPINC1 genotype in a large cohort of subjects with antithrombin inherited deficiency.

Alhenc-Gelas M, Plu-Bureau G, Hugon-Rodin J, Picard V, Horellou MH; GFHT study group on Genetic Thrombophilia. Alhenc-Gelas M, et al. Thromb Haemost. 2017 Jun 2;117(6):1040-1051. doi: 10.1160/TH16-08-0635. Epub 2017 Mar 16. Thromb Haemost. 2017. PMID: 28300866

3

Novel SERPINC1 missense mutation (Cys462Tyr) causes disruption of the 279Cys-462Cys disulfide bond and leads to type Ⅰ hereditary antithrombin deficiency.

Zhang F, Gui Y, Lu Y, Liu D, Chen H, Qin X, Li S. Zhang F, et al. Clin Biochem. 2020 Nov;85:38-42. doi: 10.1016/j.clinbiochem.2020.07.004. Epub 2020 Aug 1. Clin Biochem. 2020. PMID: 32745482

4

Molecular basis and thrombotic manifestations of antithrombin deficiency in 15 unrelated Chinese patients.

Ding Q, Wang M, Xu G, Ye X, Xi X, Yu T, Wang X, Wang H. Ding Q, et al. Thromb Res. 2013 Sep;132(3):367-73. doi: 10.1016/j.thromres.2013.07.013. Epub 2013 Aug 8. Thromb Res. 2013. PMID: 23932013

5

Antithrombin heparin binding site deficiency: A challenging diagnosis of a not so benign thrombophilia.

Orlando C, Heylen O, Lissens W, Jochmans K. Orlando C, et al. Thromb Res. 2015 Jun;135(6):1179-85. doi: 10.1016/j.thromres.2015.03.013. Epub 2015 Mar 14. Thromb Res. 2015. PMID: 25837307

6

Antithrombin deficiency in three Japanese families: one novel and two reported point mutations in the antithrombin gene.

Maruyama K, Morishita E, Karato M, Kadono T, Sekiya A, Goto Y, Sato T, Nomoto H, Omi W, Tsuzura S, Imai H, Asakura H, Ohtake S, Nakao S. Maruyama K, et al. Thromb Res. 2013 Aug;132(2):e118-23. doi: 10.1016/j.thromres.2013.06.001. Epub 2013 Jun 25. Thromb Res. 2013. PMID: 23809926

7

Subtypes of SERPINC1 mutations and the thrombotic phenotype of inherited antithrombin deficient individuals in Chinese Han population.

Wang D, Cui G, Hu S, Wang DW. Wang D, et al. Blood Cells Mol Dis. 2016 Nov;62:38-41. doi: 10.1016/j.bcmd.2016.10.029. Epub 2016 Nov 12. Blood Cells Mol Dis. 2016. PMID: 27863268

8

Circulating microparticles and the risk of thrombosis in inherited deficiencies of antithrombin, protein C and protein S.

Campello E, Spiezia L, Radu CM, Bulato C, Gavasso S, Tormene D, Woodhams B, Dalla Valle F, Simioni P. Campello E, et al. Thromb Haemost. 2016 Jan;115(1):81-8. doi: 10.1160/TH15-04-0286. Epub 2015 Sep 10. Thromb Haemost. 2016. PMID: 26354831

9

Role of antithrombin concentrate in treatment of hereditary antithrombin deficiency. An update.

Rodgers GM. Rodgers GM. Thromb Haemost. 2009 May;101(5):806-12. Thromb Haemost. 2009. PMID: 19404531 Review.

10

Molecular basis of antithrombin deficiency.

Luxembourg B, Delev D, Geisen C, Spannagl M, Krause M, Miesbach W, Heller C, Bergmann F, Schmeink U, Grossmann R, Lindhoff-Last E, Seifried E, Oldenburg J, Pavlova A. Luxembourg B, et al. Thromb Haemost. 2011 Apr;105(4):635-46. doi: 10.1160/TH10-08-0538. Epub 2011 Jan 25. Thromb Haemost. 2011. PMID: 21264449

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