Sfoglia per Autore
Allele Frequency of CYP2C9 Gene Polymorphisms in Iran
2002 F. Peyvandi, M. Spreafico, M. Karimi, S. Zeinali, P.M. Mannucci
Warfarin and acenocoumarol dose requirements according to CYP2C9 genotyping in North-Italian patients
2003 M. Spreafico, F. Peyvandi, D. Pizzotti, M. Moia, P.M. Mannucci
CYP2C9 genotypes and dose requirements during the induction phase of oral anticoagulant therapy
2004 F. Peyvandi, M. Spreafico, S.M. Siboni, M. Moia, P.M. Mannucci
International Registry of rare bleeding disorders (RBD)
2004 F. Peyvandi, M. Spreafico, M. Menegatti, I.M. Garagiola, L. Tagliabue, P.M. Mannucci
Molecular characterization in an Italian patient with plasminogen deficiency and ligneous conjunctivitis
2005 S.M. Siboni, M. Spreafico, M. Menegatti, I. Martinelli, F. Peyvandi
Relationship between CYP2C9 and VKORC1 polymorphisms and anticoagulant dose requirement
2005 M. Spreafico, F. Peyvandi, C. Lodigiani, P.M. Mannucci
Factor V and combined factor V and VIII deficiencies
2005 F. Peyvandi, M. Spreafico
Relationship between CYP2C9 and VKORC1 polymorphisms and anticoagulant dose requirement
2005 M. Spreafico, F. Peyvandi, R. Lodigiani, P.M. Mannucci
International Rare Bleeding Disorders Database
2005 F. Peyvandi, R. Palla, M. Menegatti, I. Garagiola, S.M. Siboni, P.M. Mannucci, M. Spreafico, L. Tagliabue, S. Lavoretano, A. Cairo
Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII
2005 D. Mohanty, K. Ghosh, S. Shetty, M. Spreafico, I. Garagiola, F. Peyvandi
Molecular characterization in an Italian patient with plasminogen deficiency and ligneous conjunctivitis
2005 S.M. Siboni, M. Spreafico, M. Menegatti, I. Martinelli, F. Peyvandi
Future perspective of international registry on rare inherited bleeding disorder
2006 F. Peyvandi, M. Spreafico, M. Menegatti, R. Palla, S.M. Siboni, P.M. Mannucci
Future perspective of international registry on rare inherited bleeding disorder
2006 F. Peyvandi, M. Spreafico, M. Menegatti, R. Palla, S.M. Siboni, P.M. Mannucci
Rare bleeding disorders
2006 F. Peyvandi, R.J. Kaufman, U. Seligsohn, O. Salomon, P.H. Bolton-Maggs, M. Spreafico, M. Menegatti, R. Palla, S. Siboni, P.M. Mannucci
Genetics of rare bleeding disorders
2006 F. Peyvandi, I.M. Garagiola, S. Lavoretano, M. Menegatti, R. Palla, M. Spreafico, L. Tagliabue, S. Duga, P.M. Mannucci
Genetic diagnosis of haemophilia and other inherited bleeding disorders
2006 F. Peyvandi, G. Jayandharan, M. Chandy, A. Srivastava, S.M. Nakaya, M.J. Johnson, A.R. Thompson, A. Goodeve, I. Garagiola, S. Lavoretano, M. Menegatti, R. Palla, M. Spreafico, L. Tagliabue, R. Asselta, S. Duga, P.M. Mannucci
Coagulation factor V gene analysis in five Indian patients : identification of three novel small deletions
2006 R. Asselta, C. Dall'Osso, S. Duga, M. Spreafico, R. Saxena, M.L. Tenchini
Patients Informative Booklet on the Women with rare bleeding disorders project
2007 F. Peyvandi, M. Spreafico, R. Palla, S. Lavoretano, I. Garagiola, S.M. Siboni
Molecular characterization of an Italian patient with plasminogen deficiency and ligneous conjunctivitis
2007 S.M. Siboni, M. Spreafico, M. Menegatti, I. Martinelli, F. Peyvandi
Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India
2007 G. Jayandharan, M. Spreafico, A. Viswabandya, M. Chandy, A. Srivastava, F. Peyvandi
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