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Publications by Inna Tzoran
Clinical Significance of Prothrombin G20210A Mutation in Homozygous Patients
American Journal of Hematology
Hematology
Related publications
Clinical Studies and Thrombin Generation in Patients Homozygous or Heterozygous for the G20210A Mutation in the Prothrombin Gene
Arteriosclerosis, Thrombosis, and Vascular Biology
Cardiovascular Medicine
Cardiology
Epidemiology of Prothrombin G20210a Mutation in the Mediterranean Region
Mediterranean Journal of Hematology and Infectious Diseases
Infectious Diseases
Hematology
Portal Vein Thrombosis Associated to Prothrombin G20210A Mutation and Protein C Deficiency
Clinical and Applied Thrombosis/Hemostasis
Medicine
Hematology
Type and Location of Venous Thromboembolism in Carriers of Factor v Leiden or Prothrombin G20210A Mutation Versus Patients With No Mutation
Clinical and Applied Thrombosis/Hemostasis
Medicine
Hematology
Prevalence and Geographical Variation of Prothrombin G20210A Mutation in Patients With Cerebral Vein Thrombosis: A Systematic Review and Meta-Analysis
PLoS ONE
Multidisciplinary
Prothrombin G20210A Mutation and Lower Extremity Peripheral Arterial Disease: A Systematic Review and Meta-Analysis
Journal of Vascular Surgery
Surgery
Cardiovascular Medicine
Cardiology
A C677T Methylenetetrahydrofolate Reductase (MTHFR) Polymorphism and G20210A Mutation in the Prothrombin Gene of Sickle Cell Anemia Patients From Northeast Brazil
Hemoglobin
Biochemistry
Genetics
Clinical Biochemistry
Hematology
Acute Scrotum Caused by an Extraspermatic Venous Thrombosis Associated With G20210A Prothrombin Gene Mutation in a Pediatric Patient: A Case Report
Pediatric Urology Case Reports
No Effect of the Prothrombin G20210A Mutation on Protein C Activation in a Large Kindred With Type I Protein C Deficiency
Blood Coagulation and Fibrinolysis
Medicine
Hematology
