Heterozygous prothrombin 20210G/A mutation, associated with hyperhomocysteinemia, and homozygous methylenetetrahydrofolate reductase 677C/T mutation, in a patient with portal and mesenteric venous thrombosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Biventricular Thrombi in a Patient With Heart Failure With Severely Reduced Ejection Fraction and Heterozygous Prothrombin 20210G/A and Homozygous Methylenetetrahydrofolate Reductase 677C/T Mutations;The American Journal of the Medical Sciences;2018-06
2. Trombosis venosa portal y mesentérica asociadas a hiperhomocisteinemia y anemia perniciosa en un paciente heterocigoto para la mutación C677T del gen de la MTHFR;Medicina Clínica;2011-02
3. Portal vein thrombosis in Egyptian patients with liver cirrhosis: Role of methylenetetrahydrofolate reductase C677T gene mutation;Hepatology Research;2010-03-30
4. Thrombophilia and abdominal vessel thrombosis in a Greek University hospital: A five year experience;Gastroenterology Insights;2010-01-18
5. Multiorgan involvement in a complicated case of deep vein thrombosis;Indian Journal of Gastroenterology;2009-05
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