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Last Updated: 01/07/2026
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Found 2628 publications
Congenital hypofibrinogenemia with bleeding risk: mutations in the FGA, FGB, and FGG genes.
Journal: Laboratory medicine
Published: November 14, 2025
Three new variants of the fibrinogen-related domain of the fibrinogen Bβ chain.
Journal: Thrombosis research
Published: June 25, 2025
Management of Young and Ageing Women with Afibrinogenemia and Hypofibrinogenemia.
Journal: Hamostaseologie
Published: May 27, 2025
Clinical characteristics and genotypes of patients with Congenital fibrinogen disorders
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 15, 2025
Congenital hypofibrinogenemia with a novel mutation BβCys76Phe.
Journal: The journal of medical investigation : JMI
Published: April 23, 2025
Determination of Fibrinogen Ratio Cutoff Limits Using Indirect Reference Interval Methodology.
Journal: International journal of laboratory hematology
Published: April 02, 2025
Novel variants require established frameworks: emphasizing the role of ISTH diagnostic and classification guidelines in congenital fibrinogen disorders.
Journal: Hereditas
Published: March 28, 2025
Low-Dose Dabigatran for Venous Sinus Thromboembolism Associated with Hereditary Dysfibrinogenemia: A Case Report.
Journal: British journal of hospital medicine (London, England : 2005)
Published: March 26, 2025
Placenta percreta management in a patient with a severe congenital hypofibrinogenaemia.
Journal: Annales de biologie clinique
Published: March 14, 2025
Molecular Pathogenic Mechanism Study of Two Cases of Inherited Dysfibrinogenemia
Journal: Zhongguo shi yan xue ye xue za zhi
Published: February 28, 2025
Development and validation of a risk prediction model for tigecycline-induced hypofibrinogenemia in septic patients: a retrospective cohort study.
Journal: BMC infectious diseases
Published: February 18, 2025
Last Updated: 01/07/2026