Associated Papers
[Congenital dysfibrinogenemia: current status and challenges in diagnosis and treatment].
Wang Z et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi, 2024
Congenital fibrinogen disorders: Strengthening genotype-phenotype correlations through novel genetic diagnostic tools.
Ramanan R et al.
British Journal of Haematology, 2023
One Hundred Years of Congenital Fibrinogen Disorders.
Casini A et al.
Seminars in Thrombosis and Hemostasis, 2022
Mutations Causing Mild or No Structural Damage in Interfaces of Multimerization of the Fibrinogen γ-Module More Likely Confer Negative Dominant Behaviors.
Bellacchio E
International Journal of Molecular Sciences, 2020
Fibrin(ogen) in human disease: both friend and foe.
Vilar R et al.
Haematologica, 2020
31949010 (PubMed )
Supplement: 2019.236901.VILAR_SUPPL.pdf
Can the phenotype of inherited fibrinogen disorders be predicted?
Casini A et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2016
Identification of Novel Candidate Genes for Early-Onset Colorectal Cancer Susceptibility.
de Voer RM et al.
Plos Genetics, 2016
26901136 (PubMed )
Supplement: pgen.1005880.s003.xlsx › S3_Table
Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management.
Casini A et al.
Journal of Thrombosis and Haemostasis : Jth, 2015
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