Sfoglia per Autore
Two adjacent homozygous mutations on EGF2 domain of factor X (FX) gene lead to severe FX deficiency
2006 M. Menegatti, R. Palla, F. Peyvandi
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
Dalla diagnosi di portatrice di emofilia alla diagnosi prenatale
2007 F. Peyvandi, L. Tagliabue, M. Menegatti, I.M. Garagiola, E. Santagostino
Molecular characterization of an Italian patient with plasminogen deficiency and ligneous conjunctivitis
2007 S.M. Siboni, M. Spreafico, M. Menegatti, I. Martinelli, F. Peyvandi
Database on rare bleeding disorder (RBDS) : phenotype and genotype analysis on 400 affected patients
2007 M. Spreafico, M. Menegatti, I. Garagiola, R. Palla, L. Tagliabue, M. Karimi, M. Lak, A. Srivastava, R. Saxena, S. Shetty, K. Kavakli, M.B. Dolnicar, S. Aronis Vournas, R. Asselta, S. Duga, P.M. Mannucci, F. Peyvandi
Kinetics studies of a naturally occurring mutation on Factor X (FX) gene (G222D)
2007 M. Menegatti, R. Palla, A. Afrasiabi, M. Karimi, R. De Cristofaro, F. Peyvandi
European Network of Rare Bleeding Disorders (EN-RBD)
2007 F. Peyvandi, R. Palla, M. Menegatti, S.M. Siboni, S. Halimeh, B. Faeser, H. Pergantou, H. Platokouki, P. Giangrande, K. Peerlinck, T. Celkan, N. Ozdemir, C. Bidlingmaier, J. Ingerslev, M. GIANSILY BLAIZOT, J.F. Schved, R. Gilmore, A. Gadisseur, M. BENEDIK DOLNICAR, L. Kitanovski, D. Mikovic
Establishment of a European network of rare bleeding disorders
2007 F. Peyvandi, L. Ferrario, M. Menegatti, R. Palla, M. Spreafico, K. Peerlink, T. Celkan, M. Dolnicar, J. Donadieu, S. Aronis, P. Giangrande, C. Bidlingmaier, B. White, J. Ingerslev
Recurrent mutations identified on LMAN1 and coagulation factors VII, X, XIII genes
2008 A. Cairo, M. Spreafico, M. Menegatti, I.M. Garagiola, F. Peyvandi
Phenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiency
2008 M. Karimi, M. Menegatti, A. Afrasiabi, S. Sarikhani, F. Peyvandi
State of the art of rare bleeding disorders database (RBDD)
2008 M. Spreafico, M. Menegatti, R. Palla, I. Garagiola, L. Tagliabue, A. Cairo, S. Lavoretano, R. Asselta, S. Duga, P.M. Mannucci, F. Peyvandi
Report on ten new patients with congenital Factor X deficiency and the associated mutations
2008 M. Menegatti, M. Karimi, A. Afrasiabi, F. Peyvandi
Prevalence of gain-of-function factor V Leiden and prothrombin G20210A in a large cohort of patients with rare bleeding disorders
2008 M. Menegatti, M. Spreafico, M. Karimi, S. Shetty, A. Srivastava, F. Peyvandi
Recurrent mutations identified on LMAN1 and coagulation factors VII, X, XIII genes
2008 A. Cairo, M. Menegatti, M. Spreafico, I. Garagiola, F. Peyvandi
Establishment of a European network of Rare Bleeding Disorders (RBDs)
2008 F. Peyvandi, M. Spreafico, M. Menegatti, R. Palla, A. Rocino, A. Iorio, P.M. Mannucci
Factor X deficiency
2009 M. Menegatti, F. Peyvandi
Introduction. Rare bleeding disorders : general aspects of clinical features, diagnosis, and management
2009 F. Peyvandi, R. Palla, M. Menegatti, P.M. Mannucci
Rare bleeding disorders
2010 F. Peyvandi, M. Menegatti
The role of factor X in blood coagulation : clinical, phenotypic and molecular analysis of a severe rare bleeding disorder
2010 M. Menegatti
European registry of rare bleeding disorders
2010 F. Peyvandi, R. Palla, M. Menegatti
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