Sfoglia per Autore
Mutant factor V (A19506GIn) in healthy centenarians
1996 P.M. Mannucci, F. Duca, G. Merati, F. Peyvandi, L. Tagliabue, D. Mari
Factor V (Arg 506-->Gln) mutation in young survivors of myocardial infarction
1996 D. Ardissino, F. Peyvandi, P.A. Merlini, E. Colombi, P.M. Mannucci
Autoimmune protein S deficiency and deep vein thrombosis after chickenpox
1996 F. Peyvandi, E. Faioni, G.A. Moroni, A. Rosti, L. Leo, M. Moia
Frequency of factor V Arg506 Gln in Italians
1996 P.M. Mannucci, F. Duca, F. Peyvandi, L. Tagliabue, G. Merati, I. Martinelli, M. Cattaneo
Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiency
1997 F. Peyvandi, P.M. Mannucci, D. Asti, M. Abdoullahi, N. Di Rocco, R. Sharifian
The G1456 to T mutation in the thrombomodulin gene is not frequent in patients with venous thrombosis
1997 E.M. Faioni, G. Merati, F. Peyvandi, P. Bettini, P.M. Mannucci
Gene polymorphisms predicting high plasma levels of coagulation and fibrinolysis proteins. A study in centenarians
1997 P.M. Mannucci, D. Mari, G. Merati, F. Peyvandi, L. Tagliabue, E. Sacchi, F. Taioli, P. Sansoni, S. Bertolini, C. Franceschi
Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients
1998 F. Peyvandi, P.M. Mannucci, M. Lak, M. Abdoullahi, S. Zeinali, R. Sharifian, D. Perry
Symptoms of inherited factor V deficiency in 35 Iranian patients
1998 M. Lak, R. Sharifian, F. Peyvandi, P.M. Mannucci
Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIII
1998 F. Peyvandi, E.G.D.Tuddenham, M. Akhtari, M. Lak, P.M. Mannucci
Characterization of two naturally occurring mutations in the second Epidermal Growth Factor-like domain of factor VII
1999 M. Hunault, A. Arbini, J.C. Carew, F. Peyvandi, K.A. Bauer
Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency. Blood
1999 M. Neerman Arbez, K.M. Johnson, M.A. Morris, J.H. Mcvey, F. Peyvandi, W.C. Nichols, D. Ginsburg, C. Rossier, S.E. Antonarakis, E.G.D. Tuddenham
Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia
1999 M. Lak, M. Keihani, F. Elahi, F. Peyvandi, P.M. Mannucci
Detection of DNA by silver staining
1999 D. Perry, F. Peyvandi
Rare coagulation disorders
1999 F. Peyvandi, P.M. Mannucci
Clinical manifestations and complications of childbirth and replacement therapy in 385 Iranian patients with type 3 von Willebrand disease
2000 M. Lak, F. Peyvandi, P.M. Mannucci
Apparently dominant transmission of a recessive disease: deficiency of factor VII in Iranian Jews
2000 L. Tagliabue, F. Duca, F. Peyvandi
Homozygous 2bp deletion in the human factor VII gene : a non-lethal mutation that is associated with a complete absence of circulating factor VII
2000 F. Peyvandi, P.M. Mannucci, P.V. Jenkins, A. Lee, R. Coppola, D.J. Perry
Molecular characterization and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiency
2000 F. Peyvandi, V.P. Jenkins, P.M. Mannucci, A. Billio, S. Zeinali, S.J. Perkins, D.J. Perry
Molecular characterization of a multiethnic group of 21 patients with type 3 von Willebrand disease
2000 L. Baronciani, G. Cozzi, M.T. Canciani, F. Peyvandi, A. Srivastava, A.B. Federici
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