Associated Papers
Discrepancy between international normalized ratio measurements in a heterozygous carrier of F10:p.Gly244Arg with recurrent venous thromboembolism: a case report.
Nytofte NJS et al.
Research and Practice in Thrombosis and Haemostasis, 2026
Molecular Aspects of Rare Coagulation Factor Deficiencies.
Tourbih H et al.
Cureus, 2025
Analysis of 180 Genetic Variants in a New Interactive FX Variant Database Reveals Novel Insights into FX Deficiency.
Harris VA et al.
Th Open : Companion Journal to Thrombosis and Haemostasis, 2021
Occurrence and management of severe bleeding episodes in patients with hereditary factor X deficiency.
Tarantino MD
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2021
Genetic analysis of a compound heterozygous patient with congenital factor X deficiency and regular replacement therapy with a prothrombin complex concentrate.
Togashi T et al.
International Journal of Hematology, 2020
Missense changes in the catalytic domain of coagulation factor X account for minimal function preventing a perinatal lethal condition.
Ferrarese M et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2019
Factor X Deficiency with Heterozygous Mutations of Novel p.G435S and Known p.G244R in a Patient Presenting with Severe Umbilical Hemorrhage.
Matsuo Y et al.
The Kurume Medical Journal, 2017
Efficacy of prophylaxis and genotype-phenotype correlation in patients with severe Factor X deficiency in Iran.
Karimi M et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2012
Factor X deficiency and intracranial bleeding: who is at risk?
Rauch R et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2011
Phenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiency.
Karimi M et al.
Haematologica, 2008
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