• A Case of Acquired Factor V Deficiency in Patient with Bleeding
• A case of mitral valve repair complicated by acquired factor V deficiency
• A case of Quebec platelet disorder with interstitial pneumonia
• A case of unusual acquired factor V deficiency
• A Combined Factor V and Factor VIII Deficiency: A Case Report
• A distinct common p.Gln317* mutation among causative LMAN1 genetic mutations of combined factor V and factor VIII deficiency in five Taiwanese families
• A novel mutation (Ser951LeufsTer8) in F5 gene leads to hereditary coagulation factor V deficiency
• A novel mutation of congenital factor V deficiency in Henoch-Schonlein purpura
• A Novel Phenotype of the Factor 5 Gene Mutation (Homozygote Met1736Val and Heterozygote Asp68His) Is Associated With Moderate Factor V Deficiency
• A patient with Owren disease requires pancreatic surgery: A case report
• A pilot study on the impact of congenital thrombophilia in COVID-19
• A Review of Coagulation Abnormalities of Autoimmune Acquired Factor V Deficiency with a Focus on Japan
• Acquired factor V deficiency in the setting of mercaptopurine therapy for acute lymphoblastic leukemia
• Acquired Factor V Deficiency: A New Cause of Bleeding in Patients with Chronic Myeloid Leukemia and Extreme Leukocytosis
• Acquired Factor V Deficiency: A New Cause of Bleeding in Patients with Chronic Myeloid Leukemia and Extreme Leukocytosis?
• Acquired factor V inhibitor
• Acquired factor V inhibitor with erythema and eosinophilia in a patient with end-stage renal disease
• Acute mesenteric thrombosis in a pregnant woman with Factor V Leiden mutation with a history of in vitro fertilization and embryo transfer: case report and literature review
• Altered phenotype in LMAN1-deficient mice with low levels of residual LMAN1 expression
• Analysis of a pedigree with inherited factor V deficiency caused by compound heterozygous mutation
• Analysis of phenotype and genotype of a family with hereditary coagulation factor V deficiency caused by the compound heterozygous mutations
• Autoimmune coagulation factor V/5 deficiency during chronic disseminated intravascular coagulation
• Autoimmune Factor V Deficiency That Took 16 Years to Diagnose due to Pseudodeficiency of Multiple Coagulation Factors
• Autoimmune-acquired coagulation factor V deficiency with hyperfibrinolytic disseminated intravascular coagulation
• Breaking barriers: Quebec platelet disorder
• Case Report: Novel Mutation of F5 With Maternal Uniparental Disomy Causes Severe Congenital Factor V Deficiency
• Cell therapy for factor V deficiency: An approach based on human decidua mesenchymal stem cells
• Characterization of zebrafish coagulation cofactors Fviii and Fv mutants and modeling hemophilia A and factor V deficiency
• Clinical and genetic analyses of hereditary factor Ⅴ deficiency cases
• Clinical Characterization and Molecular Analysis of Fourteen Chinese Patients with Factor V Deficiency
• Clinical features of five cases of acquired factor V deficiency
• Clinical Phenotype and Genetic Analysis of Twins With Congenital Coagulation Factor V Deficiency
• Coagulation management for a caesarean delivery in a mother with severe homozygous Factor V deficiency
• Coexisting Diseases in Patients with Familial Mediterranean Fever
• Combined deficiency of clotting factor V and factor VIII: about three siblings
• Combined Factor V and VIII Deficiency with LMAN1 Mutation: A Report of 3 Saudi Siblings
• Combined Liver-Kidney Transplant for Juvenile Polycystic Kidney Disease and Concomitant Hereditary Factor V Deficiency
• Congenital coagulation factor V deficiency with intracranial hemorrhage
• Congenital factor V deficiency in Taiwan: identification of a novel variant p.Tyr1813 ∗ and two variants specific to East Asians
• Congenital factor V deficiency in Taiwan: identification of a novel variant p.Tyr1813 and two variants specific to East Asians
• Congenital Factor V deficiency: perioperative management (case report)
• Development and Characterization of a Factor V-Deficient CRISPR Cell Model for the Correction of Mutations
• Effectiveness of the scheduled transfusion strategy for factor V deficiency with platelet dysfunction during coronary artery surgery
• EGFR-TKI-induced Factor V deficiency in a patient with advanced non-small cell lung cancer: The first case report
• Enhancer-gene rewiring in the pathogenesis of Quebec platelet disorder
• Erratum: A Review of Coagulation Abnormalities of Autoimmune Acquired Factor V Deficiency with a Focus on Japan
• F5-Atlanta: Factor V-short strikes again
• Factor V activity in apheresis platelets: Implications for management of FV deficiency
• Factor V Deficiency
• Factor V Deficiency
• Factor V Deficiency (Owren's Disease) in a Patient at High Risk for Transfusion-Associated Circulatory Overload and Bleeding During Laser Lead Extraction
• Factor V deficiency with a unique genetic mutation presenting as post-circumcision bleeding in a neonate, A-case-report
• Fatal acquired coagulation factor V deficiency after hepatectomy for advanced hepatocellular carcinoma as a possible immune checkpoint inhibitor-related adverse event: a case report
• Genetic Analysis of Hereditary Coagulation Factor V Deficiency in Two Chinese Families Caused by Compound Heterozygous Mutations
• Haemodialysis Tunisian patient with acquired factor V inhibitor associated to arteriovenous shunt thrombosis
• Hemophilia A and factor V deficiency in a girl with Turner syndrome: a case report
• Hereditary factor V deficiency from heterozygous mutations with a novel variant p.Pro798Leufs∗13 in the F5 gene
• Hereditary factor V deficiency from heterozygous mutations with a novel variant p.Pro798Leufs13 in the F5 gene
• Heterozygous large deletion mimicking homozygous substitution in MCFD2 in a patient with combined Factor V and Factor VIII deficiency
• High Mutational Heterogeneity, and New Mutations in the Human Coagulation Factor V Gene. Future Perspectives for Factor V Deficiency Using Recombinant and Advanced Therapies
• High prevalence of postpartum hemorrhage in women with rare bleeding disorders in the Netherlands: retrospective data from the RBiN study
• Identification of a novel variant of F5 gene in a consanguineous pedigree affected with inherited coagulation factor V deficiency
• Improved platelet counts during prolonged tranexamic therapy for Quebec platelet disorder implicate the underlying fibrinolytic defect as the cause of lower platelet counts
• In vitro and ex vivo rescue of a nonsense mutation responsible for severe coagulation factor V deficiency
• Intracranial Hematoma After Ventriculoperitoneal Shunt Placement in a Patient With Factor V Deficiency: A Rare Case Report
• Laparoscopic hepatectomy for hepatocellular carcinoma in a patient with congenital factor V deficiency: a case report
• Limitations of a calibrated, quantitative APC-R assay under routine conditions
• Management of a Left Atrial Appendage Thrombus Due to Atrial Fibrillation Complicating Québec Platelet Disorder
• Management of Quebec Platelet Disorder for Cervical Facet Injections in the Outpatient Setting: A Case Report
• Mining of mortality-related findings in rare bleeding disorders: a retrospective study from two centers
• Molecular and clinical characterization of two unrelated families with factor V deficiency, including a novel nonsense variant (p.Gln1532*)
• Novel splicing (c.6529-1G>T) and missense (c.1667G>A) mutations causing factor V deficiency
• Novel splicing (c.6529-1G>T) and missense (c.1667G>A) mutations causing factor V deficiency
• Owren's Disease: A Rare Deficiency
• Parahaemophilia presenting as an interesting scalp swelling
• Perioperative Management of Hereditary Factor V Deficiency: Timing of Plasma Administration is Critical in Maximizing Hemostatic Potency of Transfused Factor V
• Perioperative management of intrahepatic cholangiocarcinoma patients with hereditary coagulation factor V deficiency: a case report and literature review
• Persistent hiccups in a patient with mild congenital factor V deficiency and COVID-19; clinical and laboratory finding of a rare bleeding disorder
• Plasma Exchange as an Initial Treatment for Severe Bleeding Induced by Acquired Factor V Deficiency: A Case Report and Mini Literature Review
• Prevalence and clinical features of COVID-19 in Iranian patients with congenital coagulation disorders
• Prevalence of Factor V Leiden in a healthy population in Santa Catarina, Southern Brazil
• Rare Coagulopathies in Hematologic Spotlight: Isolated Factor V Deficiency and Combined Factor V and VIII Deficiency
• Recurrent bleeding after posthemorrhoidectomy caused by factor V deficiency: a case report and review of the literature
• Recurrent miscarriage in a woman with congenital factor V deficiency: a case report
• Severe thrombophilia in a factor V-deficient patient homozygous for the Ala2086Asp mutation (FV Besançon)
• Significance of the p.Phe218Ser and p.Gly304Glu F5 Variants in Hereditary Factor V Deficiency
• Standardization of Coagulation Factor V Reference Intervals, Prothrombin Time, and Activated Partial Thromboplastin Time in Mice for Use in Factor V Deficiency Pathological Models
• Successful correction of factor V deficiency of patient-derived iPSCs by CRISPR/Cas9-mediated gene editing
• Successful hip arthroplasty in a patient with combined deficiency of factor V and factor FVIII
• Successful management of acquired factor V deficiency developing shortly after induction of hemodialysis
• Successful Management of Life-threatening Pelvic Hemorrhage From Acquired Factor V Deficiency With immunosuppressive Therapy
• The analysis of a pedigree with hereditary coagulation factor Ⅴ deficiency caused by compound heterozygous variation of F5 gene
• The effect of factor XIa on thrombin and plasmin generation, clot formation, lysis and density in coagulation factors deficiencies
• The Magic of Proteases: From a Procoagulant and Anticoagulant Factor V to an Equitable Treatment of Its Inherited Deficiency
• The Vascular Endothelium and Coagulation: Homeostasis, Disease, and Treatment, with a Focus on the Von Willebrand Factor and Factors VIII and V
• Thrombin generation abnormalities in Quebec platelet disorder
• Thrombin generation assay is a useful pre-operative tool to predict non-bleeding risk in a patient with mild factor V deficiency
• Thromboelastometry guiding anesthetic and coagulation management of cesarean delivery in a parturient with factor V deficiency
• Transfusion-Associated Adverse Events: A Case Report of Nurse Hemovigilance and Recognition of Respiratory Distress
• Treatment of congenital coagulopathies, from biologic to biotechnological drugs: The relevance of gene editing (CRISPR/Cas)