Factor V Leiden (FVL) mutation
Factor V Leiden Mutation and its Impact on Pregnancy Complications
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Down Regulated Protein C Plasma Levels in the Absence of Factor V Leiden Mutation in HIV Patients: An Observational Study in Maiduguri, North Eastern Nigeria
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Factor V Leiden mutation triggering four major complications to standard dose cisplatin-chemotherapy for testicular seminoma: a case report
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Recurrent Pregnancy Loss in a Subject with Heterozygote Factor V Leiden Mutation; a Case Report
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The relationship of the factor V Leiden mutation or the deletion deletion polymorphism of the angiotensin converting enzyme to postoperative thromboembolic events following total joint arthroplasty
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Evaluation the frequency of factor V Leiden mutation in pregnant women with preeclampsia syndrome in an Iranian population
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Myotonic Dystrophy-1 Complicated by Factor-V (Leiden) Mutation
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Factor V Leiden mutation in relation to fecundity and miscarriage in women with venous thrombosis
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SURVEY THE MUTATION OF FGB (BETA FIBRINOGEN) AND FV (FACTOR V LEIDEN), FACTOR XIII AND FACTOR II (PROTHROMBIN), IN PATIENTS WITH RECURRENT ABORTIONS ALONG WITH NORMAL KARYOTYPEMaryam Hosseini Moghadam, Pegah Larki, Jafar Panahi, Niloofar Mojtahedifard, Abbas Shakoori*DOWNLOAD/VIEW
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Congenital anomaly of the inferior vena cava and factor V Leiden mutation predisposing to deep vein thrombosis
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Factor V Leiden, MTHFR C677T and Prothrombin Gene Mutation G20210A in Iranian Patients with Venous Thrombosis
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Impact of the factor V Leiden mutation on the outcome of pneumococcal pneumonia: a controlled laboratory study
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A case series of Factor V Leiden mutation in pregnancy
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Severe hyperhomocysteinemia due to cystathionine β-synthase deficiency, and Factor V Leiden mutation in a patient with recurrent venous thrombosis
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Relationship between Methylenetetrahydrofolate Reductase (C677T), Factor V Leiden (G1691A), Prothrombin Mutation (G20210A) and Severe Preeclampsia in a Brazilian Population
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Factor V Leiden G1691A and prothrombin G20210A mutations among Palestinian patients with sickle cell disease
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ASSOCIATION ASSESSMENT OF THROMBOPHILIC GENE MUTATIONS IN KASHMIRI WOMEN WITH RECURRENT MISCARRIAGES
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FACTOR 5 LEIDEN STUDY OF GENETIC POLYMORPHISMS AS GENETIC FACTORS THAT CAUSE CARDIOVASCULAR DISEASE IN THE POPULATION OF TABRIZ, IRAN
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Screening for genetic and acquired thrombophilia in a cohort of young migrainous patients
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