New therapy option for chronic immune thrombocytopenic purpura : a breath of fresh airRodeghiero, Francesco.European journal of haematology. Supplementum. 2009, Num 71, issn 0902-4506, 1Vol, 25 p.Book

Short- and long-term risks of splenectomy for benign haematological disorders: should we revisit the indications?RODEGHIERO, Francesco; RUGGERI, Marco.British journal of haematology. 2012, Vol 158, Num 1, pp 16-29, issn 0007-1048, 14 p.Article

Congenital von Willebrand disease type I: definition, phenotypes, clinical and laboratory assessmentRODEGHIERO, Francesco; CASTAMAN, Giancarlo.Baillière's best practice & research. Clinical haematology. 2001, Vol 14, Num 2, pp 321-335, issn 1521-6926Article

Recommended abbreviations for von Willebrand factor and its activities : On behalf of the von Willebrand Factor Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and HaemostasisMAZURIER, Claudine; RODEGHIERO, Francesco.Thrombosis and haemostasis. 2001, Vol 86, Num 2, issn 0340-6245, p. 712Article

Intraindividual consistency of the activated protein C resistance phenotypeTOSETTO, Alberto; SIMIONI, Monica; MADEO, Domenico et al.British journal of haematology. 2004, Vol 126, Num 3, pp 405-409, issn 0007-1048, 5 p.Article

Treatment of von Willebrand diseaseRODEGHIERO, Francesco; CASTAMAN, Giancarlo.Seminars in hematology. 2005, Vol 42, Num 1, pp 29-35, issn 0037-1963, 7 p.Article

Congenital absence of the inferior vena cava : a rare risk factor for idiopathic deep-vein thrombosisRUGGERI, Marco; TOSETTO, Alberto; CASTAMAN, Giancarlo et al.Lancet (British edition). 2001, Vol 357, Num 9254, issn 0140-6736, p. 441Article

Pregnancy and delivery in women with von Willebrand's disease and different von Willebrand factor mutationsCASTAMAN, Giancarlo; TOSETTO, Alberto; RODEGHIERO, Francesco et al.Haematologica (Roma). 2010, Vol 95, Num 6, pp 963-969, issn 0390-6078, 7 p.Article

Immune Thrombocytopenia in Lymphoproliferative DisordersVISCO, Carlo; RODEGHIERO, Francesco.Hematology/oncology clinics of North America. 2009, Vol 23, Num 6, issn 0889-8588, 1261-1274, vii [15 p.]Article

Heterogeneity of terminology and clinical definitions in adult idiopathic thrombocytopenic purpura : a critical appraisal from a systematic review of the literatureRUGGERI, Marco; FORTUNA, Stefania; RODEGHIERO, Francesco et al.Haematologica (Roma). 2008, Vol 93, Num 1, pp 98-103, issn 0390-6078, 6 p.Article

The VITA project : Heritability of resistance to activated protein CTOSETTO, Alberto; CASTAMAN, Giancarlo; CAPPELLARI, Antonio et al.Thrombosis and haemostasis. 2000, Vol 84, Num 5, pp 811-814, issn 0340-6245Article

How I treat von Willebrand diseaseRODEGHIERO, Francesco; CASTAMAN, Giancarlo; TOSETTO, Alberto et al.Blood. 2009, Vol 114, Num 6, pp 1158-1165, issn 0006-4971, 8 p.Article

The rate of progression to polycythemia vera or essential thrombocythemia in patients with erythrocytosis or thrombocytosisRUGGERI, Marco; TOSETTO, Alberto; FREZZATO, Maurizio et al.Annals of internal medicine. 2003, Vol 139, Num 6, pp 470-475, issn 0003-4819, 6 p.Article

Second malignancies in patients with essential thrombocythaemia treated with busulphan and hydroxyurea : long-term follow-up of a randomized clinical trialFINAZZI, Guido; RUGGERI, Marco; RODEGHIERO, Francesco et al.British journal of haematology. 2000, Vol 110, Num 3, pp 577-583, issn 0007-1048Article

Identical IGHV-D-J gene rearrangement may precede the clinical onset of chronic lymphocytic leukemia by several yearsFREZZATO, Maurizio; GIARETTA, Ilaria; MADEO, Domenico et al.American journal of hematology. 2010, Vol 85, Num 11, pp 868-871, issn 0361-8609, 4 p.Article

Assessing bleeding in von Willebrand disease with bleeding scoreTOSETTO, Alberto; CASTAMAN, Giancarlo; RODEGHIERO, Francesco et al.Blood reviews. 2007, Vol 21, Num 2, pp 89-97, issn 0268-960X, 9 p.Article

Epidemiology of von willebrand disease in developing countriesSRIVASTAVA, Alok; RODEGHIERO, Francesco.Seminars in thrombosis and hemostasis. 2005, Vol 31, Num 5, pp 569-576, issn 0094-6176, 8 p.Article

von Willebrand's disease in the year 2003: towards the complete identification of gene defects for correct diagnosis and treatmentCASTAMAN, Giancarlo; FEDERICI, Augusto B; RODEGHIERO, Francesco et al.Haematologica (Roma). 2003, Vol 88, Num 1, pp 94-108, issn 0390-6078, 15 p.Article

Association of plasma fibrinogen, C-reactive protein and G-455>A polymorphism with early atherosclerosis in the VITA Project cohortTOSETTO, Alberto; PRATI, Patrizio; BARACCHINI, Claudio et al.Thrombosis and haemostasis. 2011, Vol 105, Num 2, pp 329-335, issn 0340-6245, 7 p.Article

Recurrence of the 'deep-intronic' FGG IVS6-320A>T mutation causing quantitative fibrinogen deficiency in the Italian population of VenetoPLATE, Manuela; DUGA, Stefano; CASTAMAN, Giancarlo et al.Blood coagulation & fibrinolysis. 2009, Vol 20, Num 5, pp 381-384, issn 0957-5235, 4 p.Article

Bleeding tendency and efficacy of anti-haemorrhagic treatments in patients with type 1 von Willebrand disease and increased von Willebrand factor clearanceCASTAMAN, Giancarlo; TOSETTO, Alberto; FEDERICI, Augusto B et al.Thrombosis and haemostasis. 2011, Vol 105, Num 4, pp 647-654, issn 0340-6245, 8 p.Article

Autoimmune hemolytic anemia in patients with chronic lymphocytic leukemia is associated with IgVH statusVISCO, Carlo; NOVELLA, Elisabetta; PEOTTA, Eleonora et al.Haematologica (Roma). 2010, Vol 95, Num 7, pp 1230-1232, issn 0390-6078, 3 p.Article

Evidence-based diagnosis of type 1 von Willebrand disease : a Bayes theorem approach. CommentaryABBOTT, Diana; DI PAOLA, Jorge; TOSETTO, Alberto et al.Blood. 2008, Vol 111, Num 8, issn 0006-4971, 3919-3920, 3998-4003 [8 p.]Article

A novel family with recessive von Willebrand disease due to compound heterozygosity for a splice site mutation and a missense mutation in the von Willebrand factor geneCASTAMAN, Giancarlo; NOVELLA, Elisabetta; CASTIGLIA, Evelina et al.Thrombosis research. 2002, Vol 105, Num 2, pp 135-138, issn 0049-3848Article

Isolated erythrocytosis: study of 67 patients and identification of three novel germ-line mutations in the prolyl hydroxylase domain protein 2 (PHD2) geneALBIERO, Elena; RUGGERI, Marco; FORTUNA, Stefania et al.Haematologica (Roma). 2012, Vol 97, Num 1, pp 123-127, issn 0390-6078, 5 p.Article