Disease: Flaujeac factor deficiency
- A hitherto undescribed plasma factor acting at the contact phase of blood coagulation (Flaujeac factor): case report and coagulation studies
- A novel frameshift mutation in exon 4 causing a deficiency of high-molecular-weight kininogen in a patient with splenic infarction
- Factor XII deficiency - Hageman trait. Additional diagnostic procedures
- Flaujeac factor deficiency. Reconstitution with highly purified bovine high molecular weight-kininogen and delineation of a new permeability-enhancing peptide released by plasma kallikrein from bovine high molecular weight-kininogen
- Flaujeac trait. Deficiency of human plasma kininogen
- Hereditary deficiency of a new coagulation factor acting at the "contact" level: the "Flaujeac" factor
- Participation of Hageman factor dependent pathways in human disease states
- Severe high-molecular-weight kininogen deficiency due to a homozygous c.1456C > T nonsense variant in a large Chinese family
- Severe high-molecular-weight kininogen deficiency: clinical characteristics, deficiency-causing KNG1 variants, and estimated prevalence
- The First Korean Case of High-Molecular-Weight Kininogen Deficiency, With a Novel Variant, c.488delG, in the <em>KNG1</em> Gene