Familial Hypofibrinogenemia Latest Advances

Repair of severe hand injury by acellular dermal matrix: a rare case of hypofibrinogenaemia resulting in hand injury after haemangioma resection.

Journal: Journal of wound care

Published: February 07, 2026

Bleeding from umbilicus in a neonate: exploring aetiologies of a common presentation.

Journal: BMJ case reports

Published: February 05, 2026

Functional and structural consequences of fibrinogen γ-chain variants associated with thrombotic phenotype in congenital fibrinogen disorders.

Journal: Thrombosis research

Published: January 23, 2026

Unexpected fibrinogen impairment detected by rotational thromboelastometry in a 76-year-old patient undergoing brain tumor resection: A case report.

Journal: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

Published: January 18, 2026

Incidence and risk factors of tocilizumab-induced hypofibrinogenemia in patients with thyroid eye disease: a single-center retrospective study.

Journal: Frontiers in endocrinology

Published: January 05, 2026

A novel missense variant (c.1172A>T, p.Asn391Ile) in the gamma chain of fibrinogen causing hypodysfibrinogenemia in an asymptomatic Danish family and review of adjacent variants.

Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis

Published: December 03, 2025

Congenital hypofibrinogenemia with bleeding risk: mutations in the FGA, FGB, and FGG genes.

Journal: Laboratory medicine

Published: November 14, 2025

Impact of eravacycline on fibrinogen.

Journal: The Journal of antimicrobial chemotherapy

Published: October 30, 2025

Clinical outcomes and health-system challenges in congenital afibrinogenemia: a single-centre prospective case series.

Journal: Blood cells, molecules & diseases

Published: October 05, 2025

Fibrinogen replacement to prevent intracranial hemorrhage in ischemic stroke patients after thrombolysis - a prospective randomized open blinded endpoint trial (FibER): rationale and methods.

Journal: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association

Published: July 09, 2025

Novel and known fibrinogen gene mutations in Chinese pediatric patients with congenital dysfibrinogenemia: genetic and functional characterization.

Journal: Clinical biochemistry

Published: June 28, 2025

Three new variants of the fibrinogen-related domain of the fibrinogen Bβ chain.

Journal: Thrombosis research

Published: June 25, 2025

Familial Hypofibrinogenemia Latest Advances

Find the Latest Research About Familial Hypofibrinogenemia

Repair of severe hand injury by acellular dermal matrix: a rare case of hypofibrinogenaemia resulting in hand injury after haemangioma resection.

Repair of severe hand injury by acellular dermal matrix: a rare case of hypofibrinogenaemia resulting in hand injury after haemangioma resection.

Bleeding from umbilicus in a neonate: exploring aetiologies of a common presentation.

Bleeding from umbilicus in a neonate: exploring aetiologies of a common presentation.

Functional and structural consequences of fibrinogen γ-chain variants associated with thrombotic phenotype in congenital fibrinogen disorders.

Functional and structural consequences of fibrinogen γ-chain variants associated with thrombotic phenotype in congenital fibrinogen disorders.

Unexpected fibrinogen impairment detected by rotational thromboelastometry in a 76-year-old patient undergoing brain tumor resection: A case report.

Unexpected fibrinogen impairment detected by rotational thromboelastometry in a 76-year-old patient undergoing brain tumor resection: A case report.

Incidence and risk factors of tocilizumab-induced hypofibrinogenemia in patients with thyroid eye disease: a single-center retrospective study.

Incidence and risk factors of tocilizumab-induced hypofibrinogenemia in patients with thyroid eye disease: a single-center retrospective study.

A novel missense variant (c.1172A>T, p.Asn391Ile) in the gamma chain of fibrinogen causing hypodysfibrinogenemia in an asymptomatic Danish family and review of adjacent variants.

A novel missense variant (c.1172A>T, p.Asn391Ile) in the gamma chain of fibrinogen causing hypodysfibrinogenemia in an asymptomatic Danish family and review of adjacent variants.

Congenital hypofibrinogenemia with bleeding risk: mutations in the FGA, FGB, and FGG genes.

Congenital hypofibrinogenemia with bleeding risk: mutations in the FGA, FGB, and FGG genes.

Impact of eravacycline on fibrinogen.

Impact of eravacycline on fibrinogen.

Clinical outcomes and health-system challenges in congenital afibrinogenemia: a single-centre prospective case series.

Clinical outcomes and health-system challenges in congenital afibrinogenemia: a single-centre prospective case series.

Fibrinogen replacement to prevent intracranial hemorrhage in ischemic stroke patients after thrombolysis - a prospective randomized open blinded endpoint trial (FibER): rationale and methods.

Fibrinogen replacement to prevent intracranial hemorrhage in ischemic stroke patients after thrombolysis - a prospective randomized open blinded endpoint trial (FibER): rationale and methods.

Novel and known fibrinogen gene mutations in Chinese pediatric patients with congenital dysfibrinogenemia: genetic and functional characterization.

Novel and known fibrinogen gene mutations in Chinese pediatric patients with congenital dysfibrinogenemia: genetic and functional characterization.

Three new variants of the fibrinogen-related domain of the fibrinogen Bβ chain.

Three new variants of the fibrinogen-related domain of the fibrinogen Bβ chain.