P. Di Perna

A novel G-to-A mutation in the intron-N of the protein S gene leading to abnormal RNA splicing in a patient with protein S deficiency.

M. Margaglione, G. Cibelli, G. Di Minno, 2003, Haematologica.

Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin.

M. Margaglione, E. Grandone, M. Chetta, 2004, Haematologica.

BNT162b2 mRNA COVID-19 Vaccine Does Not Impact the Honeymoon Phase in Type 1 Diabetes: A Case Report

C. Ricordi, A. Feraco, M. Infante, 2022, Vaccines.

A new case of combined factor V and factor VIII deficiency further suggests that the LMAN1 M1T mutation is a frequent cause in Italian patients.

M. Margaglione, R. Santacroce, P. Di Perna, 2007, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin.

M. Margaglione, E. Grandone, R. Santacroce, 2005, Blood.

Identification of six novel mutations in type I antithrombin deficient Italian families.

M. Margaglione, G. D’Andrea, V. Brancaccio, 2004, Haematologica.

Protein Z gene polymorphisms are associated with protein Z plasma levels

M. Margaglione, F. Sessa, R. Santacroce, 2004, Journal of thrombosis and haemostasis : JTH.

High risk for microcarcinoma in thyroid benign diseases. Incidence in a one year period of total thyroidectomies.

M. Carlini, P. Di Perna, M. Passeri, 2005, Journal of experimental & clinical cancer research : CR.

A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin.

M. Margaglione, E. Grandone, R. Santacroce, 2005, Blood.