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Prothrombin G20210A
Mutation in the Prothrombin Gene G20210A As a Cause of Cerebral Venous Thrombosis
The Underrecognized Prothrombotic Vascular Disease of COVID-19
Spontaneous Deep Vein Thrombosis in Hemophilia A: a Case Report Murat Bicer, Murat Yanar* and Oktay Tuydes
Thrombocytopenia and Intracranial Venous Sinus Thrombosis After “COVID-19 Vaccine Astrazeneca” Exposure
Disseminated Intravascular Coagulation and Coagulation Disorders Carl-Erik Dempfle
OFC Vol. 17/4
1 FACTOR V LEIDEN, PROTHROMBIN G20210A, and MTHFR
Outcomes of Genetic Testing in Adults with a History of Venous Thromboembolism
Is Inherited Thrombophilia a Risk Factor for Arterial Stroke?
Laboratory Bulletin... Updates and Information from Rex Healthcare and Rex Outreach
Prothrombin G20210A Mutation
Factor II (Prothrombin) 20210 G -->A
Factor II/Prothrombin Testing for Thrombophilia
Prothrombin Gene G20210A Mutation and Obstetric Complications
Acute Quadriplegia in a Young Man Secondary to Prothrombin G20210A Mutation
AndProthrombinGeneMutation
Acute Myocardial Infarction in a Child: Possible Pathogenic Role of Patent Foramen Ovale Associated with Heritable Thrombophilia
Molecular Testing for Coagulation Disorders
Top View
Hypercoagulability Syndromes
Review the Prothrombin G20210A Mutation - a Common Cause of Thrombophilia? Die Prothrombin G20210A-Mutation - Häufige Ursache Thrombophiler Diathesen?
Perinatal/Neonatal Case Presentation
Genetic Testing for Hereditary and Multifactorial Conditions
Genetic Testing for Hereditary Thrombophilia Product Applicability
Prothrombin G20210A Mutation Genetic Testing Consent Form
Prothrombotic Risk Mutations and Polymorphisms in Patients with Hemophilia a – a Preliminary Study
Induced Thrombotic Thrombocytopenia in Australia
MTHFR Gene Polymorphisms and Cardiovascular Risk Factors, Clinical-Imagistic Features and Outcome in Cerebral Venous Sinus Thrombosis
Factor II/Prothrombin Testing for Thrombophilia
Pregnancy Complications in G20210A Mutation Carriers Associated with High Prothrombin Activity
©Ferrata Storti Foundation
Factor V Leiden, Prothrombin G20210A Substitution and Hormone
Risk of Venous Thrombosis in Carriers of the Prothrombin G20210A Variant
Upper Limb Deep Vein Thrombosis in Patient with Hemophilia a and Heterozygosity for Prothrombin G20210A: a Case Report and Review of the Literature
Venous Thrombosis CLINICAL VALIDITY
Prevention of Venous Thromboembolism in 2020 and Beyond
Can Factor V Leiden
Do Prothrombotic Factors Influence Clinical Phenotype of Severe Haemophilia? a Review of the Literature Karin Van Dijk1,2, Johanna G
Draft Genetic Test Review[PDF 987KB]
The Case for Personalized Medicine
GENE.00046 Prothrombin G20210A (Factor II) Mutation Testing
Factor V Leiden G1691A and Prothrombin Gene G20210A Mutations on Pregnancy Outcome
The Genetics of Thrombophilia Written By: Elizabeth Varga, M.S.*
Handouts Hypercoagulable States.Pdf
Role of Factor V Leiden, Prothrombin G20210A
Prothrombin Gene Mutation (G20210a)
Prothrombin Thrombophilia
Factor II/Prothrombin Testing for Thrombophilia