Rare Bleeding DisordersPEYVANDI, Flora.Seminars in thrombosis and hemostasis. 2009, Vol 35, Num 4, issn 0094-6176, 103 p.Serial Issue

Factor V DeficiencyASSELTA, Rosanna; PEYVANDI, Flora.Seminars in thrombosis and hemostasis. 2009, Vol 35, Num 4, pp 382-389, issn 0094-6176, 8 p.Article

Factor X DeficiencyMENEGATTI, Marzia; PEYVANDI, Flora.Seminars in thrombosis and hemostasis. 2009, Vol 35, Num 4, pp 407-415, issn 0094-6176, 9 p.Article

Combined Factor V and Factor VIII DeficiencySPREAFICO, Marta; PEYVANDI, Flora.Seminars in thrombosis and hemostasis. 2009, Vol 35, Num 4, pp 390-399, issn 0094-6176, 10 p.Article

Results of an international, multicentre pharmacokinetic trial in congenital fibrinogen deficiencyPEYVANDI, Flora.Thrombosis research. 2009, Vol 124, issn 0049-3848, S9-S11, SUP2Conference Paper

Introduction: Rare Bleeding Disorders: General Aspects of Clinical Features, Diagnosis, and ManagementPEYVANDI, Flora; PALLA, Roberta; MENEGATTI, Marzia et al.Seminars in thrombosis and hemostasis. 2009, Vol 35, Num 4, pp 349-355, issn 0094-6176, 7 p.Article

Factor XI DeficiencyDUGA, Stefano; SALOMON, Ophira.Seminars in thrombosis and hemostasis. 2009, Vol 35, Num 4, pp 416-425, issn 0094-6176, 10 p.Article

Congenital Prothrombin DeficiencyLANCELLOTTI, Stefano; DE CRISTOFARO, Raimondo.Seminars in thrombosis and hemostasis. 2009, Vol 35, Num 4, pp 367-381, issn 0094-6176, 15 p.Article

Novel aspects of factor XIII deficiencyMUSZBEK, László; BAGOLY, Zsuzsa; CAIRO, Andrea et al.Current opinion in hematology. 2011, Vol 18, Num 5, pp 366-372, issn 1065-6251, 7 p.Article

Carrier detection and prenatal diagnosis of hemophilia in developing countriesPEYVANDI, Flora.Seminars in thrombosis and hemostasis. 2005, Vol 31, Num 5, pp 544-554, issn 0094-6176, 11 p.Article

Factor VII DeficiencyMARIANI, Guglielmo; BERNARDI, Francesco.Seminars in thrombosis and hemostasis. 2009, Vol 35, Num 4, pp 400-406, issn 0094-6176, 7 p.Article

Pitfalls in molecular diagnosis in a family with severe factor VII (FVII) deficiency: misdiagnosis by direct sequence analysis using a PCR productGARAGIOLA, Isabella; PALLA, Roberta; PEYVANDI, Flora et al.Prenatal diagnosis. 2003, Vol 23, Num 9, pp 731-734, issn 0197-3851, 4 p.Article

Congenital Fibrinogen DisordersDE MOERLOOSE, Philippe; NEERMAN-ARBEZ, Marguerite.Seminars in thrombosis and hemostasis. 2009, Vol 35, Num 4, pp 356-366, issn 0094-6176, 11 p.Article

Recessively inherited coagulation disordersMANNUCCI, Pier Mannuccio; DUGA, Stefano; PEYVANDI, Flora et al.Blood. 2004, Vol 104, Num 5, pp 1243-1252, issn 0006-4971, 10 p.Article

Factor XI deficiency in Iranians: Its clinical manifestations in comparison with those of classic hemophiliaPEYVANDI, Flora; LAK, Manueh; MANNUCCI, Pier Mannuccio et al.Haematologica (Roma). 2002, Vol 87, Num 5, pp 512-514, issn 0390-6078Article

Factor XIII DeficiencyKARIMI, Mehran; BERECZKY, Zsuzsanna; COHAN, Nader et al.Seminars in thrombosis and hemostasis. 2009, Vol 35, Num 4, pp 426-438, issn 0094-6176, 13 p.Article

Phenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiencyKARIMI, Mehran; MENEGATTI, Marzia; AFRASIABI, Abdolreza et al.Haematologica (Roma). 2008, Vol 93, Num 6, pp 934-938, issn 0390-6078, 5 p.Article

A rare inherited coagulation disorder: Combined homozygous factor VII and factor X deficiencyMENEGATTI, Marzia; KARIMI, Mehran; GARAGIOLA, Isabella et al.American journal of hematology. 2004, Vol 77, Num 1, pp 90-91, issn 0361-8609, 2 p.Article

Bleeding symptoms in heterozygous carriers of inherited coagulation disorders in southern IranMAHMOODI, Mojtaba; PEYVANDI, Flora; AFRASIABI, Abdolreza et al.Blood coagulation & fibrinolysis. 2011, Vol 22, Num 5, pp 396-401, issn 0957-5235, 6 p.Article

Molecular characterization of an italian patient with plasminogen deficiency and ligneous conjunctivitisSIBONI, Simona M; SPREAFICO, Marta; MENEGATTI, Marzia et al.Blood coagulation & fibrinolysis. 2007, Vol 18, Num 1, pp 81-84, issn 0957-5235, 4 p.Article

Molecular and functional characterization of a natural homozygous Arg67His mutation in the prothrombin gene of a patient with a severe procoagulant defect contrasting with a mild hemorrhagic phenotypeAKHAVAN, Sepideh; DE CRISTOFARO, Raimondo; PEYVANDI, Flora et al.Blood. 2002, Vol 100, Num 4, pp 1347-1353, issn 0006-4971, 7 p.Article

Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in indian families with combined deficiency of factor V and VIIIMOHANTY, Dipika; GHOSH, Kanjaksha; SHETTY, Shrimati et al.American journal of hematology. 2005, Vol 79, Num 4, pp 262-266, issn 0361-8609, 5 p.Article

Thrombosis in inflammatory bowel diseases : Role of inherited thrombophiliaSPINA, Luisa; SAIBENI, Simone; BATTAGLIOLI, Tullia et al.The American journal of gastroenterology. 2005, Vol 100, Num 9, pp 2036-2041, issn 0002-9270, 6 p.Article

Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bβ-chain gene causing activation of cryptic splice sitesSPENA, Silvia; DUGA, Stefano; ASSELTA, Rosanna et al.Blood. 2002, Vol 100, Num 13, pp 4478-4484, issn 0006-4971, 7 p.Article

Discrepancies between ADAMTS13 activity assays in patients with thrombotic microangiopathiesMACKIE, Ian; LANGLEY, Katy; CHITOLIE, Andrew et al.Thrombosis and haemostasis. 2013, Vol 109, Num 3, pp 488-496, issn 0340-6245, 9 p.Article