Associated Papers
Three new variants of the fibrinogen-related domain of the fibrinogen Bβ chain.
Kotlín R et al.
Thrombosis Research, 2025
Dysfibrinogenemia and hypofibrinogenemia - Spectrum of pathogenic variants in Slovak patients.
Jaraskova D et al.
Biomedical Papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia, 2025
Mutations Accounting for Congenital Fibrinogen Disorders: An Update.
Richard M et al.
Seminars in Thrombosis and Hemostasis, 2022
Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype.
Simurda T et al.
International Journal of Molecular Sciences, 2020
Perioperative management of a severe congenital hypofibrinogenemia with thrombotic phenotype.
Simurda T et al.
Thrombosis Research, 2020
Human Fibrinogen: Molecular and Genetic Aspects of Congenital Disorders.
Tiscia GL et al.
International Journal of Molecular Sciences, 2018
Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders.
Simurda T et al.
International Journal of Molecular Sciences, 2017
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