Sfoglia per Autore
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
A novel polymorphism in intron 1a of the human factor VII gene (G73A): study of a healthy Italian population and of 190 young survivors of myocardial infarction
2000 F. Peyvandi, P.M. Mannucci, P. Bucciarelli, S. Zeinali, S. Akhavan, E. Sacchi, P.A. Merlini, D.J. Perry
Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs
2001 R. Asselta, S. Duga, S. Spena, E. Santagostino, F. Peyvandi, G. Piseddu, R. Targhetta, M. Malcovati, P.M. Mannucci, M.L. Tenchini
Autosomal recessive deficiency of coagulation factors
2001 F. Peyvandi, R. Asselta, P.M. Mannucci
Abnormal secretion and function of recombinant human factor VII as the result of modification to a calcium binding site caused by a 15 base pair insertion in the factor VII gene
2001 F. Peyvandi, J.A. Carew, D.J. Perry, M. Hanault, U. Khanduri, S.J. Perkins, P.M. Mannucci, K.A. Bauer
Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bbeta-chain gene causing activation of cryptic splice sites
2002 S. Spena, S. Duga, R. Asselta, M. Malcovati, F. Peyvandi, M.L. Tenchini
Factor XI deficiency in Iranians: its clinical manifestations in comparison with those of classic hemophilia
2002 F. Peyvandi, M. Lak, P.M. Mannucci
Rare coagulation deficiencies
2002 F. Peyvandi, S. Duga, S. Akhavan, P.M. Mannucci
Short-term exposure to high altitude causes coagulation activation and inhibits fibrinolysis
2002 P.M. Mannucci, A. Gringeri, F. Peyvandi, T. Di Paolantonio, M. Mariani
Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency
2002 F. Peyvandi, M. Menegatti, E. Santagostino, S. Akhavan, J. Uprichard, D.J. Perry, S.J. Perkins, P.M. Mannucci
Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia
2002 R. Asselta, S. Spena, S. Duga, F. Peyvandi, M. Malcovati, P.M. Mannucci, M.L. Tenchini
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 phenotype
2002 S. Akhavan, R. De Cristofaro, F. Peyvandi, S. Lavoretano, R. Landolfi, P.M. Mannucci
Relatively poor performance of clinical laboratories for DNA analyses in the detection of two thrombophilic mutations : a cause for concern
2002 A. Tripodi, F. Peyvandi, V. Chantarangkul, M. Menegatti, P.M. Mannucci
The thrombogram in rare inherited coagulation disorders: its relation to clinical bleeding
2002 R. Al Dieri, F. Peyvandi, E. Santagostino, M. Giansily, P.M. Mannucci, J.F. Schved, S. Beguin, C.H. Hemker
Two Naturally Occurring Mutations on FVII Gene (S363I-W364C) Altering Intrinsic Catalytic Activity
2002 F. Peyvandi, R. De Cristofaro, S. Akhavan, J.A. Carew, R. Landolfi, K.A. Bauer, P.M. Mannucci
Allele Frequency of CYP2C9 Gene Polymorphisms in Iran
2002 F. Peyvandi, M. Spreafico, M. Karimi, S. Zeinali, P.M. Mannucci
Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patients
2003 L. Baronciani, G. Cozzi, M.T. Canciani, F. Peyvandi, A. Srivastava, A.B. Federici, P.M. Mannucci
Patients with localized and disseminated tumors have reduced but measurable levels of ADAMTS-13 (von Willebrand factor cleaving protease)
2003 P.M. Mannucci, M. Karimi, A. Mosalaei, M.T. Canciani, F. Peyvandi
Vagaries of genetic association studies in myocardial infarction
2003 P.M. Mannucci, D. Ardissino, P.A. Merlini, F. Peyvandi
Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency : molecular characterization by expression of the recombinant protein
2003 S. Duga, M.C. Montefusco, R. Asselta, M. Malcovati, F. Peyvandi, E. Santagostino, P.M. Mannucci, M.L. Tenchini
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