• A Case of Autoimmune Hepatitis Complicated by Undiagnosed Factor VII Deficiency: A Pitfall of Coagulopathy
• A case-report of the unprovoked thrombotic event in a patient with thymoma and severe FVII deficiency
• A multicenter, observational study to evaluate hemostasis following recombinant activated FVII treatment in patients in Japan with congenital factor VII deficiency
• A Rare Case of Acquired Factor VIII Deficiency in an Elderly Male With a History of Rheumatoid Arthritis
• A Rare Case of Hemophilia: Acquired Factor VIII Deficiency
• Acquired Factor VII Deficiency Associated With Chronic Myeloid Leukemia Blast Crisis
• Acquired factor VII deficiency in pediatric inflammatory bowel disease: Report of three cases
• Acquired Hemophilia A and ST-Elevation Myocardial Infarction (STEMI): A Rare Presentation and Management Dilemma
• Acquired Hemophilia A: Bleeding Pattern and Hemostatic Therapeutic Strategies
• Acquired isolated factor VII deficiency in a patient with myxoid pleomorphic liposarcoma, case report
• Acquired Isolated Factor VII Deficiency in Plasma Cell Dyscrasias: A Brief Presentation of Two Plasma-Cell-Leukemia-Related Cases and Review of Literature
• Activation of TrkB signaling mitigates cerebellar anomalies caused by Rbm4-Bdnf deficiency
• Acute Thrombotic Events in Association With Coronavirus Disease of 2019 Immunization as Initial Presentation of Congenital Factor VII Deficiency
• Analysis of three Chinese pedigrees affected with Hereditary factor deficiency due to compound heterozygous variants of F7 gene
• Anesthetic management with labor epidural analgesia of the parturient with severe factor VII deficiency: a case report
• Bleeding disorder of unknown cause: Results from Iranian study
• Cardiac Rhabdomyomas Presenting with Critical Cardiac Obstruction in Neonates and Infants: Treatment Strategies and Outcome, A Single-Center Experience
• Cardiovascular Disease and Thrombosis: Intersections with the Immune System, Inflammation, and the Coagulation System
• 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
• Coronary Artery Bypass Grafting in a Patient With Severe Factor VII Deficiency
• Current status and future prospects of activated recombinant coagulation factor VIIa, NovoSeven®, in the treatment of haemophilia and rare bleeding disorders
• Diffuse alveolar hemorrhage after hematopoietic cell transplantation- response to treatments and risk factors for mortality
• Does a preoperative coagulation sheet change the postoperative bleeding rate after adenoidectomy?
• Factor V Deficiency
• Factor VII Deficiency and Second Trimester Abortion: A Case Report
• Factor VII Deficiency in an End-Stage Renal Disease Patient With Recurrent Thrombosis: A Case Report
• Factor VII Deficiency in Systemic Mastocytosis with an Associated Myeloid Neoplasm
• Falsely prolonged prothrombin time test in a patient with erythrocytosis: a case report
• Feto-Maternal Outcomes in Pregnancy With Factor VII Deficiency in a Tertiary Care Institution
• Frequency of the p.Thr241Asn mutation in Chinese patients with congenital factor VII deficiency
• Genetic Landscape of Factor VII Deficiency: Insights from a Comprehensive Analysis of Pathogenic Variants and Their Impact on Coagulation Activity
• Genotype-Phenotype Relationship among 785 Unrelated White Women with Inherited Congenital Factor VII Deficiency: A Three-Center Database Study
• Gynecological bleeding in women with congenital bleeding disorders: A comprehensive cohort from Iran
• Hereditary coagulation factor VII deficiency caused by novel compound heterozygous mutations c.572-1G>A and c.1037A>C in a Chinese pedigree
• Inherited coagulation factor VII deficiency in Taiwan: Two novel F7 variants with relevant regional features in 33 patients
• Interleukin 10, but not tumor necrosis factor-alpha, gene variations are associated with factor VII inhibitor development
• Joint deficiency of coagulation factors VII and IX: a case report
• Krüppel-like factor 7 deficiency disrupts corpus callosum development and neuronal migration in the developing mouse cerebral cortex
• Management of erythropoietic protoporphyria with cholestatic liver disease: A case report
• Mild FVII deficiency - Correlation between genotype and phenotype
• Molecular Genetic Analysis of Russian Patients with Coagulation Factor FVII Deficiency
• Naringin corrects renal failure related to Lesch-Nyhan disease in a rat model via NOS-cAMP-PKA and BDNF/TrkB pathways
• Nasal hemophilic pseudotumor in a 2-year-old with recurrent epistaxis: a case report and review of the literature
• Patient with congenital factor VII deficiency undergoing brain tumor neurosurgery successfully treated with recombinant factor VIIa and fresh frozen plasma: A case report and literature review
• Perioperative ROTEM evaluation in a patient affected by severe VII factor deficiency undergoing microvascular decompression craniotomy for hemifacial spasm
• Prothrombin Time and International Normalized Ratio as Predictors of Factor VII Coagulation Activity in Pediatric Patients
• Rare bleeding disorders: Real-world data from a Spanish tertiary hospital
• 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
• Site-directed mutagenesis of tissue factor pathway inhibitor-binding exosite D60A on factor VII results in a new factor VII variant with lower coagulant activity
• Spontaneous renal rupture caused by factor VII deficiency: A case report
• Synonymous variant at the terminal nucleotide in exon 3 of F7 causes abnormal splicing: A case report
• The effect of factor XIa on thrombin and plasmin generation, clot formation, lysis and density in coagulation factors deficiencies
• The identification of a novel compound heterozygous mutation in hereditary human coagulation factor VII deficiency following a bamboo leaf green snake bite
• The rare case of double valve surgery in a patient with factor VII deficiency
• Type VII Collagen Deficiency in the Oncogenesis of Cutaneous Squamous Cell Carcinoma in Dystrophic Epidermolysis Bullosa
• Undiagnosed Factor VII Deficiency in Cardiac Surgery Complicated by Bleeding: A Case Report
• Utility of ACMG classification to support interpretation of molecular genetic test results in patients with factor VII deficiency
• Viscoelastic testing guided coagulation management in factor VII deficiency for spinal anaesthesia and caesarean section