• "Familial Multiple Coagulation Factor Deficiencies of FXI and FXII in an Asymptomatic Saudi Woman"
• A Case Report of a Hemodialysis Patient With Coagulation Factor XI and Factor XII Deficiencies
• A Case Report of Severe Factor XI Deficiency during Cardiac Surgery: Less Can Be More
• A comprehensive insight into the role of zinc deficiency in the renin-angiotensin and kinin-kallikrein system dysfunctions in COVID-19 patients
• A Novel Homozygous Missense Mutation (Ile583Asn) in a Consanguineous Marriage Family with Hereditary Factor XII Deficiency: A Case Report
• A novel homozygous missense mutation (Met527Ile) in a consanguineous marriage family with inherited factor XII deficiency
• A quantitative systems pharmacology model of plasma kallikrein-kinin system dysregulation in hereditary angioedema
• A Rare Cause of Isolated Prolonged Activated Partial Thromboplastin Time: An Overview of Prekallikrein Deficiency and the Contact System
• Amelioration of Cognitive and Behavioral Deficits after Traumatic Brain Injury in Coagulation Factor XII Deficient Mice
• An Analysis of the Sensitivity of the Activated Partial Thromboplastin Time (APTT) Assay, as Used in a Large Laboratory Network, to Coagulation Factor Deficiencies
• An unanticipated prolonged baseline ACT during cardiac surgery due to factor XII deficiency
• An update on factor XII-driven vascular inflammation
• An Update on Safe Anticoagulation
• Analysis of a Chinese pedigree affected with Hereditary coagulation factor deficiency due to compound heterozygous variants of F12 gene
• Analysis of a Chinese pedigree affected with Hereditary coagulation factor Ⅻ deficiency due to compound heterozygous variants of F12 gene
• 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 A Pedigree with Hereditary Coagulation Factor Deficiency Caused by Compound Heterozygous Mutations
• Analysis of A Pedigree with Hereditary Coagulation Factor Ⅻ Deficiency Caused by Compound Heterozygous Mutations
• Analysis of F12 gene variants and molecular mechanisms in patients with coagulation factor deficiency
• Analysis of F12 gene variants and molecular mechanisms in patients with coagulation factor Ⅻ deficiency
• Analysis of Hereditary FXII Deficiency Caused by Three Mutations Including a Novel Mutation
• Angioedema Without Wheals: Challenges in Laboratorial Diagnosis
• Autoimmune Factor V Deficiency That Took 16 Years to Diagnose due to Pseudodeficiency of Multiple Coagulation Factors
• Biochemistry, molecular genetics, and clinical aspects of hereditary angioedema with and without C1 inhibitor deficiency
• C1 esterase inhibitor-mediated immunosuppression in COVID-19: Friend or foe?
• Cardiopulmonary bypass in a child with severe Factor XII deficiency
• Cardiovascular risk factors, haemostasis and antithrombotic treatment in retinal vessel occlusion
• Case Report: An Adult Patient With Deficiency of Adenosine Deaminase 2 Resembled Unilateral Frosted Branch Angiitis
• Characterization of congenital factor XII deficiency in Taiwanese patients: identification of one novel and one common mutation
• Clinical and genetic features of hereditary angioedema with and without C1-inhibitor (C1-INH) deficiency in Japan
• Clinical Outcomes after Biologic Graft Use for the Creation of Blalock-Taussig Shunt in Critically Ill Patients with Thrombophilia
• Coagulation Abnormalities in Light Chain Amyloidosis
• Collagen XII Deficiency Increases the Risk of Anterior Cruciate Ligament Injury in Mice
• Congenital hemophilia A with low activity of factor XII: a case report and literature review
• Emerging drugs for the treatment of hereditary angioedema due to C1-inhibitor deficiency
• Endovenous Thermal Ablation for a Varicose Vein Patient with Factor XII Deficiency: A Case Report
• Factor V Deficiency
• Factor XI, much more than an innocent observer
• Factor XII and prekallikrein promote microvascular inflammation and psoriasis in mice
• Factor XII deficiency evaluated by thrombin generation assay
• Factor XII deficiency in asymptomatic Saudi population: A retrospective cohort study
• Factor XII Deficiency in Mexico: High Prevalence in the General Population and Patients with Venous Thromboembolic Disease
• Factor XII deficiency: a clinical and molecular genetic study
• Factor XII promotes the thromboinflammatory response in a rat model of veno-arterial extracorporeal membrane oxygenation
• Factor XII promotes the thromboinflammatory response in a rat model of venoarterial extracorporeal membrane oxygenation
• Factor XII(a) inhibitors: a review of the patent literature
• Familial Multiple Coagulation Factor Deficiencies (FMCFDs) in a Large Cohort of Patients-A Single-Center Experience in Genetic Diagnosis
• Fatal acquired coagulation factor V deficiency after hepatectomy for advanced hepatocellular carcinoma as a possible immune checkpoint inhibitor-related adverse event: a case report
• Friend or Foe: Factor XII Deficiency Discovered Incidentally during Management of NSTEMI
• Genetic analysis of a Chinese pedigree affected with Congenital coagulation factor XII deficiency due to a c.1A>G start codon variant of F12 gene
• Genetic analysis of a Chinese pedigree affected with Congenital coagulation factor XII deficiency due to a c.1A>G start codon variant of F12 gene
• Genetic analysis of a pedigree with hereditary coagulation factor XII deficiency
• Hereditary Angioedema With Normal C1 Inhibitor: US Survey of Prevalence and Provider Practice Patterns
• Hereditary Angioedema: Diagnosis, Clinical Implications, and Pathophysiology
• Hereditary angioedema: Investigational therapies and future research
• Hereditary factor XII deficiency in an adult patient: A case report
• High molecular weight kininogen interactions with the homologs prekallikrein and factor XI: importance to surface-induced coagulation
• High-molecular-weight kininogen interactions with the homologs prekallikrein and factor XI: importance to surface-induced coagulation
• Homozygous missense variant F12 (Gly506Asp) associated with severe factor XII deficiency: a case report
• In-vivo functions and regulation of polyphosphate in the vascular system
• Incidence of factor XII deficiency in critically ill patients with a prolonged activated partial thromboplastin time: a prospective observational study
• Inheritance Pattern of Hereditary Angioedema Indicates Mutation-Dependent Selective Effects During Early Embryonic Development
• Investigation on abnormal gene loci of a Chinese pedigree with hereditary combined deficiency of blood coagulation factor XI, XII, and protein S
• Long-term Prophylaxis with Androgens in the management of Hereditary Angioedema (HAE) in emerging countries
• Mast cell degranulation and bradykinin-induced angioedema - searching for the missing link
• Mechanism, Functions, and Diagnostic Relevance of FXII Activation by Foreign Surfaces
• Mechanisms involved in hereditary angioedema with normal C1-inhibitor activity
• New perspective of anticoagulation in intensive care unit: basic and clinical advances in coagulation factor XII and XI inhibitors
• Pathophysiology of Hereditary Angioedema (HAE) Beyond the SERPING1 Gene
• Pedigree Analysis of Hereditary Coagulation Factor XII Deficiency Caused by Compound Heterozygous Mutation p.Gly175Cys and p.Gly542Ser of F12 Gene
• Periodic Severe Angioedema without Exogenous Hormone Exposure
• Phenotypic and genetic analyses of four cases of coagulation factor XII deficiency
• Plasmin-mediated cleavage of high-molecular-weight kininogen contributes to acetaminophen-induced acute liver failure
• Polyphosphate expression by cancer cell extracellular vesicles mediates binding of factor XII and contact activation
• Preoperative bleeding risk assessment with ISTH-BAT and laboratory tests in patients undergoing elective surgery: A prospective cohort study
• Prevalence of FXII-Deficiency and Its Relevance to Monitoring Anticoagulation in Adults Receiving Extracorporeal Membrane Oxygenation
• Prolonged activated partial thromboplastin time secondary to factor XII deficiency in two surgical patients
• Prolonged APTT secondary to factor XII deficiency in a patient with prostate cancer: A case report
• Protein disulfide isomerase cleaves allosteric disulfides in histidine-rich glycoprotein to regulate thrombosis
• Safety of Tonsillectomy and/or Adenoidectomy in Pediatric Patients with Prolonged Activated Partial Thromboplastin Time and Factor XII Deficiency
• Severe Prekallikrein Deficiency Associated with Low Level of Factor XII: A Case Report
• Survey of actual conditions of erythema marginatum as a prodromal symptom in Japanese patients with hereditary angioedema
• Systemic inflammation biomarkers during angioedema attacks in hereditary angioedema
• The characteristics of upper airway edema in hereditary and acquired angioedema with C1-inhibitor deficiency
• The complex role of kininogens in hereditary angioedema
• The effect of estrogen-containing birth control pills on the constituents of bradykinin expression in plasma
• The Expanding Spectrum of Mutations in Hereditary Angioedema
• The future of therapeutic options for hereditary angioedema
• The FXII c.-4T>C Polymorphism as a Disease Modifier in Patients With Hereditary Angioedema Due to the FXII p.Thr328Lys Variant
• The Genetics of Hereditary Angioedema: A Review
• The Standard Point-of-Care Hemochron Jr. ACT+ Test in Monitoring Heparin Administration for Cardiopulmonary Bypass in Severe Factor XII Deficiency
• Transient acquired factor XII deficiency associated with moderately severe Covid-19 pneumonia
• Treatment of Hereditary Angioedema
• Trimethylamine N-oxide (TMAO) drives insulin resistance and cognitive deficiencies in a senescence accelerated mouse model
• Two Novel Mutations (<em>G774A</em> and <em>A1685G</em>) Causing Coagulation Factor XII Deficiency in a Patient with Acute Inferior Myocardial Infarction
• Two Novel Mutations (G774A and A1685G) Causing Coagulation Factor XII Deficiency in a Patient with Acute Inferior Myocardial Infarction
• Unnecessary Abdominal Surgeries in Attacks of Hereditary Angioedema with Normal C1 Inhibitor
• Usefulness of Routine Coagulation Tests in Healthy Children Undergoing Elective Minor Surgery: a 12-Year Retrospective Study
• Whole-exome sequencing reveals a novel frameshift mutation in a consanguineous family with a hereditary coagulation factor XII deficiency