• "Prothrombin conversion and thrombin decay in patients with cirrhosis-role of prothrombin and antithrombin deficiencies": comment
• "Prothrombin conversion and thrombin decay in patients with cirrhosis-role of prothrombin and antithrombin deficiencies": comment from de Laat-Kremers et al
• A Case of Autoimmune Hepatitis Complicated by Undiagnosed Factor VII Deficiency: A Pitfall of Coagulopathy
• A Case of Congenital Mild Hemophilia Diagnosed After Wisdom Teeth Extraction
• A Case of Significant Coagulopathy Due to Vitamin K Deficiency Caused by the Administration of Cefazolin and Rifampicin and Hyponutrition After a Postoperative Infection of the Lumbar Spine
• A case of suspected lupus anticoagulant-hypoprothrombinemia syndrome in a boy due to mycoplasma infection
• A nonneutralizing antibody as cause of prothrombin deficiency in a patient with follicular lymphoma
• A Novel Variant of the LMAN1 Gene in Combined Factor V and Factor VIII Deficiency in a Saudi Female Child: A Case Report
• A Rare Case of Hemophilia: Acquired Factor VIII Deficiency
• A retrospective study of the prevalence of isolated prolongation of activated partial thromboplastin time in the preoperative setting
• A super-geriatric patient with gastrostomy underwent life-threatening prothrombin time-international normalized ratio prolongation by warfarin following fasting and antibiotic therapy
• Acquired Factor VIII Deficiency in Chronic Myeloid Leukemia: A Case Report
• Acquired Factor X Deficiency without Amyloidosis Presenting with Massive Hematuria: A Case Report and Review of the Literature
• Acquired Hemophilia A: Bleeding Pattern and Hemostatic Therapeutic Strategies
• Analysis of a Chinese pedigree affected with Hereditary F deficiency due to compound heterozygous variants of F12 gene
• Analysis of a Chinese pedigree affected with Hereditary FⅫ deficiency due to compound heterozygous variants of F12 gene
• Analysis of three Chinese pedigrees affected with Hereditary factor deficiency due to compound heterozygous variants of F7 gene
• Antithrombin Deficiency Is Associated with Prothrombotic Plasma Fibrin Clot Phenotype
• Assessment of coagulation assays on Roche Cobas t711 analyzer: performance and clinical implications
• Association of Broad-Spectrum Antibiotic Therapy and Vitamin E Supplementation with Vitamin K Deficiency-Induced Coagulopathy: A Case Report and Narrative Review of the Literature
• Association of single nucleotide polymorphisms (4G/5G) of plasminogen activator inhibitor-1 and the risk factors for placenta-related obstetric complications
• Auto-validation of Routine Coagulation/Hemostasis Assays with Reflex Testing of Abnormal Test Results
• Autoimmune Hepatitis Complicated by Undiagnosed Factor VII Deficiency: A Pitfall of Coagulopathy
• Circulating Inhibitor against Factor X: A Rare Cause of Hemorrhagic Diathesis
• Clinical outcome and neurological development of patients with biliary atresia associated with a bleeding tendency: a single institution experience
• Clot Waveform Analysis for Hemostatic Abnormalities
• Coagulation abnormalities in a prospective cohort of 50 patients with PMM2-congenital disorder of glycosylation
• Concurrent Deficiency of Factor V and Factor VIII in a Pediatric Patient: A Case Report
• Congenital F Deficiency Associated with a Novel Mutation in F7 Gene
• Congenital Factor X-Riyadh (Stuart-Prower) Deficiency With Isolated Prothrombin Time Prolongation: A Case Report
• Congenital thrombophilia in East-Asian venous thromboembolism population: a systematic review and meta-analysis
• Development and validation of a nomogram for predicting cefoperazone/sulbactam-induced hypoprothrombinaemia in Hospitalized adult patients
• Endothelial dysfunction, thrombophilia, and nailfold capillaroscopic features in livedoid vasculopathy
• Evaluation of acquired and hereditary risk factors for the development of thromboembolism in patients with systemic lupus erythematosus
• Factor V Deficiency
• Factor V variants in bleeding and thrombosis
• Falsely prolonged prothrombin time test in a patient with erythrocytosis: a case report
• Fitusiran reduces bleeding in factor X-deficient mice
• Genotype-Phenotype Relationship among 785 Unrelated White Women with Inherited Congenital Factor VII Deficiency: A Three-Center Database Study
• Hemophilia A and factor V deficiency in a girl with Turner syndrome: a case report
• High prevalence of thrombophilic risk factors in patients with central retinal artery occlusion
• Hypoprothrombinemia-lupus anticoagulant syndrome secondary to Sjogren's syndrome: A case report
• Increased thromboinflammatory load in hereditary angioedema
• Inflammasome activation and pyroptosis mediate coagulopathy and inflammation in Salmonella systemic infection
• International Council for Standardization in Haematology Field Study Evaluating Optimal Interpretation Methods for Activated Partial Thromboplastin Time and Prothrombin Time Mixing Studies
• Isolated Prothrombin Deficiency: A Case Report of a Rare Coagulation Disorder and Review of Literature
• Joint deficiency of coagulation factors VII and IX: a case report
• Kinetic analysis of prothrombinase assembly and substrate delivery mechanisms
• Laboratory Testing for von Willebrand Disease Using a Composite Rapid 3-Test Chemiluminescence-Based von Willebrand Factor Assay Panel
• Late Onset Vitamin K Deficiency Bleeding in a Neonate and Role of Elevated PIVKA-II Levels
• Lupus anticoagulant hypoprothrombinemia syndrome with multiple and high-titer antiphospholipid antibodies strongly interfered with coagulation assays
• Lupus Anticoagulant Testing: Dilute Prothrombin Time (dPT)
• Lupus anticoagulant-hypoprothrombinemia syndrome in children: Three case reports and systematic review of the literature
• Lupus Anticoagulant-Hypoprothrombinemia Syndrome: Literature Review and Description of Local Case in a 3-Year-Old Chinese Girl
• Management of Acquired Factor X Deficiency Caused by In Vitro Non-neutralizing Anti-factor X Autoantibodies with Pre-emptive Corticosteroid Therapy
• Management of Thrombosis in a Patient with Three Thrombophilic Disorders
• Microsurgical breast reconstruction and primary hypercoagulable disorders
• Navigating the Challenges of Factor X Deficiency: A Case Study
• Neonatal Purpura Fulminans in a Patient With Arterial Thrombosis and Congenital Renal Agenesis
• New predictors of microvascular invasion for small hepatocellular carcinoma ≤ 3 cm
• New Triazole-Based Potent Inhibitors of Human Factor XIIa as Anticoagulants
• No Detectable Coagulation Activation After Vitamin K (MK-7) Supplementation in Patients on Dialysis With Functional Vitamin K Deficiency: A One-Year Randomized, Placebo-Controlled Study
• Outcomes of venous thromboembolism in patients with inherited thrombophilia treated with direct oral anticoagulants: insights from the RIETE registry
• Performance and Interpretation of Clot Waveform Analysis
• Phenotype and genotype analyses of two pedigrees with inherited fibrinogen deficiency
• Phenotypic and genetic analysis of a Chinese pedigree affected with Hereditary antithrombin deficiency due to a novel variant of SERPINC1 gene
• Plasma-derived human factor X concentrate for the treatment of patients with hereditary factor X deficiency
• Platelet-Derived TGF-β1 Promotes Deep Vein Thrombosis
• Post-viral idiopathic purpura fulminans is associated with inherited thrombophilia and anti-cardiolipin antibodies
• Protection of β2GPI Deficient Mice from Thrombosis Reflects a Defect in PAR3-facilitated Platelet Activation
• Protein induced by vitamin K absence or antagonist II: Experience to date and future directions
• Prothrombin Complex Concentrate
• Prothrombin deficiency with recurrent subretinal hemorrhage
• Prothrombin Time and International Normalized Ratio as Predictors of Factor VII Coagulation Activity in Pediatric Patients
• Quantification of the contribution of individual coagulation factors to haemostasis using a microchip flow chamber system and reconstituted blood from deficient plasma
• Rapid diagnosis of coagulopathies from vitamin K deficiency in a consecutive case cohort evaluated by comparative assessment of factor II by one stage assays with prothrombin time versus Ecarin reagents
• Recurrent MiscarriageGreen-top Guideline No. 17
• Resolution of cardiac surgical bleeding with the combination of 4-factor prothrombin complex concentrate and fresh frozen plasma following lack of response to fresh frozen plasma alone in a patient with severe factor XI deficiency
• Right femoral vein and right dorsal artery thrombosis in childhood acute myeloid leukemia: A case report
• Role of individual factor X concentrate pharmacokinetic studies in perioperative management of AL amyloidosis-associated acquired factor X deficiency
• ROTEM could be useful for lupus anticoagulant hypoprothrombinemia syndrome
• Severe acquired hemophilia A associated with COVID-19 vaccination: A case report and literature review
• Severe Early-Onset Vitamin K Deficiency Bleeding in a Neonate Born to a Mother with Crohn's Disease in Clinical Remission: A Case Report
• Sheehan's Syndrome in a Patient With Factor XI Deficiency
• The Effect of Vitamin K2 Supplementation on PIVKA-II Levels in Patients with Severe Motor and Intellectual Disabilities Undergoing Long-Term Tube Feeding
• The identification of a novel compound heterozygous mutation in hereditary human coagulation factor VII deficiency following a bamboo leaf green snake bite
• The influence of hematological profiles on the transfusion management and mortality risk of mothers presenting to the obstetric unit of a South African tertiary medical facility
• The safety of the combination therapy of recombinant factor VIIa and plasma-derived factor VIIa and factor X for refractory hemorrhage in acquired hemophilia A
• The use of vitamin K for coagulopathy in critically ill children
• The utility of the dilute prothrombin time in the interpretation of antiphospholipid syndrome testing
• Thromboelastography
• Thrombophilia Testing in Stroke: A Case Report and Review of Evidence
• Transcriptomic Meta-Analysis Identifies Upregulated Clotting and Fibrinolysis Pathways in Colorectal Cancer Tumors Containing Hereditary PMS2 Mismatch Repair Deficiency
• Validation for the function of protein C in mouse models
• Varicella-associated disseminated intravascular coagulation secondary to Henoch-Schönlein purpura with renal and gastrointestinal system involvement in a child: A case report
• Venous thromboembolism risk in adults with hereditary thrombophilia: a systematic review and meta-analysis
• Vitamin K insufficiency and the prophylaxis strategy in term healthy infants: A multicentre study
• Vitamin K Status Based on K1, MK-4, MK-7, and Undercarboxylated Prothrombin Levels in Adolescent and Adult Patients with Cystic Fibrosis: A Cross-Sectional Study
• Von Willebrand factor levels in healthy blood donors and their association with blood group: A tertiary care hospital-based study
• Zinc supplementation with polaprezinc was associated with improvements in albumin, prothrombin time activity, and hemoglobin in chronic liver disease