D-Dimer and Portal Vein Status in Splenectomized Egyptian β-Thalassemia Major Patients: A Prospective Single–Thalassemia Center Experience
Author:
Publisher
Informa UK Limited
Subject
Oncology,Hematology,Pediatrics, Perinatology and Child Health
Link
http://www.tandfonline.com/doi/pdf/10.3109/08880018.2011.645186
Reference26 articles.
1. ?-Thalassaemia and sickle cell anaemia as paradigms of hypercoagulability
2. Prevalence of thromboembolic events among 8,860 patients with thalassaemia major and intermedia in the Mediterranean area and Iran
3. THALASSEMIA AND VENOUS THROMBOEMBOLISM
4. Overview on practices in thalassemia intermedia management aiming for lowering complication rates across a region of endemicity: the OPTIMAL CARE study
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1. Thromboembolism in Beta-Thalassemia Disease;Beta Thalassemia;2020-09-23
2. A Comparison of Hemostatic Changes in Splenectomized and Nonsplenectomized β-Thalassemia Intermedia Patients;Journal of Pediatric Hematology/Oncology;2016-11
3. Hypercoagulable state as demonstrated by thromboelastometry in hemoglobin E/beta-thalassemia patients: Association with clinical severity and splenectomy status;Thrombosis Research;2016-04
4. Portal vein thrombosis after laparoscopic splenectomy during childhood;Journal of Thrombosis and Thrombolysis;2013-12-14
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