Glanzmann's thrombasthenia: modulation of clinical phenotype by α2C807T gene polymorphismD'ANDREA, Giovanna; MARGAGLIONE, Maurizio.Haematologica (Roma). 2003, Vol 88, Num 12, pp 1378-1382, issn 0390-6078, 5 p.Article

Oral anticoagulants : Pharmacogenetics Relationship between genetic and non-genetic factorsD'ANDREA, Giovanna; D'AMBROSIO, Rosa; MARGAGLIONE, Maurizio et al.Blood reviews. 2008, Vol 22, Num 3, pp 127-140, issn 0268-960X, 14 p.Article

The factor V (FV) gene ASP79HIS polymorphism modulates FV plasma levels and affects the activated protein C resistance phenotype in the presence of the FV Leiden mutationBOSSONE, Anna; CAPPUCCI, Filomena; D'ANDREA, Giovanna et al.Haematologica (Roma). 2003, Vol 88, Num 3, pp 286-289, issn 0390-6078, 4 p.Article

Interleukin 28B Gene Polymorphisms in Hepatitis C Virus-related Cryoglobulinemic VasculitisSANSONNO, Domenico; RUSSI, Sabino; SERVIDDIO, Gaetano et al.Journal of rheumatology. 2014, Vol 41, Num 1, pp 91-98, issn 0315-162X, 8 p.Article

Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarinD'AMBROSIO, Rosa Lucia; D'ANDREA, Giovanna; CAPPUCCI, Filomena et al.Haematologica (Roma). 2004, Vol 89, Num 12, pp 1510-1516, issn 0390-6078, 7 p.Article

A novel G-to-A mutation in intron-N of the protein S gene leading to abnormal rna splicing in a patient with protein S deficiencyD'ANDREA, Giovanna; DI PERNA, Pasquale; BRANCACCIO, Vincenzo et al.Haematologica (Roma). 2003, Vol 88, Num 4, pp 459-464, issn 0390-6078, 6 p.Article

A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarinD'ANDREA, Giovanna; D'AMBROSIO, Rosa Lucia; DI PERNA, Pasquale et al.Blood. 2005, Vol 105, Num 2, pp 645-649, issn 0006-4971, 5 p.Article

Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domainD'ANDREA, Giovanna; BOSSONE, Anna; LUPONE, Maria Rosaria et al.Haematologica (Roma). 2004, Vol 89, Num 8, pp 979-984, issn 0390-6078, 6 p.Article

High prevalence of thrombophilic genotypes in patients with acute mesenteric vein thrombosisAMITRANO, Lucio; BRANCACCIO, Vincenzo; GUARDASCIONE, Maria Anna et al.The American journal of gastroenterology. 2001, Vol 96, Num 1, pp 146-149, issn 0002-9270Article

A β3 Asp217→Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin αIIBβ3 functionsD'ANDREA, Giovanna; BAFUNNO, Valeria; DEL VECCHIO, Luigi et al.Blood coagulation & fibrinolysis. 2008, Vol 19, Num 7, pp 657-662, issn 0957-5235, 6 p.Article

FV HR2 Haplotype as additional inherited risk Factor for deep vein thrombosis in individuals with a high-risk profileMARGAGLIONE, Maurizio; BOSSONE, Anna; COALIZZO, Donatella et al.Thrombosis and haemostasis. 2002, Vol 87, Num 1, pp 32-36, issn 0340-6245Article

Glanzmann's thrombasthenia: Identification of 19 new mutations in 30 patientsD'ANDREA, Giovanna; COLAIZZO, Donatella; VECCHIONE, Gennaro et al.Thrombosis and haemostasis. 2002, Vol 87, Num 6, pp 1034-1042, issn 0340-6245Article

Genetic modulation of oral anticoagulation with warfarinMARGAGLIONE, Maurizio; COLAIZZO, Donatella; D'ANDREA, Giovanna et al.Thrombosis and haemostasis. 2000, Vol 84, Num 5, pp 775-778, issn 0340-6245Article