Author:
Casoria Aniello,Miele Ciro,Capasso Filomena,Mormile Rosaria,Bisceglia Luigi,Pracella Riccardo,Vecchione Gennaro,Cirillo Ferdinando,Frangipane Ignazio,Conca Paolo,Cimino Ernesto,Di Minno Matteo,Tufano Antonella
Reference10 articles.
1. Human fibrinogen: molecular and genetic aspects of congenital disorders;Tiscia;Int. J. Mol. Sci.,2018
2. Identification of novel mutations in patients with fibrinogen disorders and genotype/phenotype correlations;Chinni;Blood Transfus.,2019
3. Diagnosis of congenital fibrinogen disorders;Lebreton;Ann. Biol. Clin. (Paris),2016
4. Diagnosis and classification of congenital fibrinogen disorders: communication from the SSC of the ISTH;Casini;J. Thromb. Haemost.,2018
5. Comparison of the fibrinogen Clauss assay and the fibrinogen PT derived method in patients with dysfibrinogenemia;Miesbach;Thromb. Res.,2010