Factor 10 Deficiency Latest Advances

Hereditary Combined Deficiency of Vitamin K-Dependent Clotting Factors Presenting as Postoperative Haemorrhage in A Syrian Adolescent: A Likely VKCFD Type 2 Phenotype.

Journal: European journal of case reports in internal medicine

Published: October 22, 2025

Characterization of a novel factor X variant, p.F139L, associated with bleedings in heterozygous and compound heterozygous form.

Journal: Thrombosis research

Published: May 22, 2025

Characterization and management of patients with hereditary factor X deficiency: A case series.

Journal: Transfusion

Published: April 18, 2025

The global epidemiology of acquired factor X deficiency.

Journal: Hematology (Amsterdam, Netherlands)

Published: March 28, 2025

Severe Congenital Factor X Deficiency as a First Case Report in Cambodia.

Journal: Case reports in hematology

Published: March 14, 2025

Acquired FX deficiency: a case report and literature review

Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi

Published: March 03, 2025

Gastrointestinal Bleeding From Acquired Factor X Deficiency due to Light Chain Amyloidosis.

Journal: Gastro hep advances

Published: February 25, 2025

Navigating polycythemia vera and factor X deficiency on cardiopulmonary bypass for coronary artery bypass grafting: a case report.

Journal: The journal of extra-corporeal technology

Published: January 23, 2025

Bleeding Patterns and Clinical Outcomes in Patients With Systemic AL Amyloidosis-Related Acquired Factor X Deficiency.

Journal: American journal of hematology

Published: January 15, 2025

Factor X Concentrate Treatment Schedule and Dosing in Acquired FX Deficiency.

Journal: Hematology reports

Published: December 03, 2024

Phylogenetic analysis and pathogenesis study of a new deletion mutation causing inherited FⅩ deficiency

Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi

Published: December 02, 2024

Case report: a case of AL amyloidosis with spontaneous giant retroperitoneal hematoma.

Journal: International journal of emergency medicine

Published: October 20, 2024

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Hereditary Combined Deficiency of Vitamin K-Dependent Clotting Factors Presenting as Postoperative Haemorrhage in A Syrian Adolescent: A Likely VKCFD Type 2 Phenotype.

Hereditary Combined Deficiency of Vitamin K-Dependent Clotting Factors Presenting as Postoperative Haemorrhage in A Syrian Adolescent: A Likely VKCFD Type 2 Phenotype.

Characterization of a novel factor X variant, p.F139L, associated with bleedings in heterozygous and compound heterozygous form.

Characterization of a novel factor X variant, p.F139L, associated with bleedings in heterozygous and compound heterozygous form.

Characterization and management of patients with hereditary factor X deficiency: A case series.

Characterization and management of patients with hereditary factor X deficiency: A case series.

The global epidemiology of acquired factor X deficiency.

The global epidemiology of acquired factor X deficiency.

Severe Congenital Factor X Deficiency as a First Case Report in Cambodia.

Severe Congenital Factor X Deficiency as a First Case Report in Cambodia.

Acquired FX deficiency: a case report and literature review

Acquired FX deficiency: a case report and literature review

Gastrointestinal Bleeding From Acquired Factor X Deficiency due to Light Chain Amyloidosis.

Gastrointestinal Bleeding From Acquired Factor X Deficiency due to Light Chain Amyloidosis.

Navigating polycythemia vera and factor X deficiency on cardiopulmonary bypass for coronary artery bypass grafting: a case report.

Navigating polycythemia vera and factor X deficiency on cardiopulmonary bypass for coronary artery bypass grafting: a case report.

Bleeding Patterns and Clinical Outcomes in Patients With Systemic AL Amyloidosis-Related Acquired Factor X Deficiency.

Bleeding Patterns and Clinical Outcomes in Patients With Systemic AL Amyloidosis-Related Acquired Factor X Deficiency.

Factor X Concentrate Treatment Schedule and Dosing in Acquired FX Deficiency.

Factor X Concentrate Treatment Schedule and Dosing in Acquired FX Deficiency.

Phylogenetic analysis and pathogenesis study of a new deletion mutation causing inherited FⅩ deficiency

Phylogenetic analysis and pathogenesis study of a new deletion mutation causing inherited FⅩ deficiency

Case report: a case of AL amyloidosis with spontaneous giant retroperitoneal hematoma.

Case report: a case of AL amyloidosis with spontaneous giant retroperitoneal hematoma.