Alpha 2-antiplasmin deficiency in a Sudanese child: a case report
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[1] Congenital alpha2-antiplasmin deficiency , 2020, Definitions.
[2] M. Nijziel,et al. Hemorrhagic disorders of fibrinolysis: a clinical review , 2018, Journal of thrombosis and haemostasis : JTH.
[3] Publisher's Note , 2018, Anaesthesia.
[4] D. Rijken,et al. Inhibition of Fibrinolysis by Coagulation Factor XIII , 2017, BioMed research international.
[5] A. Kaider,et al. Fibrinolysis in patients with a mild-to-moderate bleeding tendency of unknown cause , 2016, Annals of Hematology.
[6] A. Houng,et al. α2-Antiplasmin: New Insights and Opportunities for Ischemic Stroke , 2016, Seminars in Thrombosis and Hemostasis.
[7] J. Hirose,et al. Total hip arthroplasty and total knee arthroplasty in a patient with congenital deficiency of plasminogen activator inhibitor‐1 , 2016, Haemophilia.
[8] F. Leebeek,et al. Natural heterogeneity of α2-antiplasmin: functional and clinical consequences. , 2016, Blood.
[9] S. Yasar Yildiz,et al. Functional Stability of Plasminogen Activator Inhibitor-1 , 2014, TheScientificWorldJournal.
[10] T. Terao,et al. Life‐threatening hemorrhage and prolonged wound healing are remarkable phenotypes manifested by complete plasminogen activator inhibitor‐1 deficiency in humans , 2011, Journal of thrombosis and haemostasis : JTH.
[11] S. L. Carpenter,et al. α2‐Antiplasmin and its deficiency: fibrinolysis out of balance , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.