Association of factor V Leiden, Janus kinase 2, prothrombin, and MTHFR mutations with primary Budd-Chiari syndrome in Egyptian patients
Author:
Affiliation:
1. Department of Medical Biochemistry; Faculty of Medicine; Menoufia University; Shibin El Kom Egypt
2. Department of Tropical Medicine, Faculty of Medicine; Menoufia University; Shibin El Kom Egypt
Publisher
Wiley
Subject
Gastroenterology,Hepatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/jgh.13066/fullpdf
Reference41 articles.
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2. Strategy and long-term outcomes of endovascular treatment for Budd-Chiari syndrome complicated by inferior vena caval thrombosis;Zhang;Eur. J. Vasc. Endovasc. Surg.,2014
3. Primary Budd-Chiari syndrome;Valla;J. Hepatol.,2009
4. JAK2 V617F mutation and 46/1 haplotype in Chinese Budd-Chiari syndrome patients;Wang;J. Gastroenterol. Hepatol.,2014
5. Clinical approach to splanchnic vein thrombosis: risk factors and treatment;Riva;Thromb. Res.,2012
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