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Titolo Data di pubblicazione Autore(i) File
Factor V Leiden is associated with premature myocardial infarction 1-gen-2008 Peyvandi, F.; Spreafico, M.; Foco, L.; Bernardinelli, L.; Duga, S.; Asselta, R.; Ardissino, D.; Kathiresan, S.; Merlini, P. A.; Mannucci, P. M.
Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern 1-gen-2008 Dall'Osso, C.; Guella, I.; Duga, S.; Locatelli, N.; Paraboschi, E. M.; Spreafico, M.; Afrasiabi, A.; Pechlaner, C.; Peyvandi, F.; Tenchini, M. L.; Asselta, R.; Paraboschi, Elvezia Maria
Factor XI gene mutations in factor XI deficient patients of the Czech Republic 1-gen-2008 Castaman, G; Giacomelli, S. H.; Habart, D; Asselta, R; Duga, S; Rodeghiero, F
Severe factor XI deficiency in the Abruzzo region of Italy is associated to different FXI gene mutations 1-gen-2008 Castaman, G.; Giacomelli, S. H.; Dragani, A.; Iuliani, O.; Duga, S.; Rodeghiero, F.
Molecular characterization of six novel mutations causing factor V deficiency 1-gen-2008 Guella, I.; Paraboschi, E.; Duga, S.; Peyvandi, F.; Song, J.; Ciavarella, N.; Mannucci, P. M.; Asselta, R.
Molecular characterization of two novel mutations causing factor XI deficiency : a splicing defect and a missense mutation responsible for a CRM+ defect 1-gen-2008 Guella, I.; Solda', G.; Spena, S.; Asselta, R.; Ghiotto, R.; Tenchini, M. L.; Castaman, G.; Duga, S.
Identification and characterization of 6 novel genetic defects leading to factor V deficiency 1-gen-2008 Guella, I; Paraboschi, Em; Duga, S; Asselta, R
Characterization of productive and unproductive mRNA splicings in F11: identification of a novel coagulation FXI isoform 1-gen-2008 Rimoldi, V; Guella, I; Asselta, R; De Cristofaro, R; Peyvandi, F; Mannucci, Pm; Duga, S
Mutations leading to premature termination codons in the Von Willebrand factor gene are associated with allele-specific mRNAs decay 1-gen-2008 Plate’, M; Duga, S; Baronciani, L; Federici, Ab; Asselta, R
Mutations leading to premature termination codons in the Von Willebrand factor gene are associated with the decay of the mutant mRNAs 1-gen-2008 Plate’, M; Duga, S; Baronciani, L; Federici, Ab; Asselta, R
Identification and characterization of 6 novel genetics defects leading to factor V deficiency 1-gen-2008 Guella, I; Paraboschi, E; Duga, S; Asselta, R
Simultaneous genotyping of coagulation factor XI type II and type III mutations by multiplex real-time polymerase chain reaction to determine their prevalence in healthy and factor XI-deficient Italians 1-gen-2008 Zadra, G.; Asselta, R.; Tenchini, M. L.; Castaman, G.; Seligsohn, U.; Mannucci, P. M.; Duga, S.
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 1-gen-2008 Dall’Osso, C; Rizzo, G; Solda', G; Gemmati, D; Zamboni, P; Benedetti, Md; Salviati, A; Invernizzi, P; Bonissoni, S; Bolognesi, E; Bergamaschi, L; D’Alfonso, S; Duga, S; Tenchini, Ml; Asselta, R.
Factor V Leiden, but not prothrombin G20120A, is associated with premature myocardial infarction 1-gen-2008 Spreafico, M.; Peyvandi, F.; Foco, L.; Bernardinelli, L.; Duga, S.; Asselta, R.; Ardissino, D.; Kathiresan, S.; Merlini, P. A.; Mannucci, P. M.
Functional analysis of missense mutations in the Myocyte Enhancer Factor 2A (MEF2A) gene do not support their causal role in the pathogenesis of myocardial infarction 1-gen-2008 Guella, I; Rimoldi, V; Merlini, Pa; Asselta, R; Paraboschi, Em; Francolini, M; Peyvandi, F; Ardissimo, D; Mannucci, Pm; Duga, S
Reply to: [Factor XI mutation and the origin of Ashkenazi Jews. Haematologica 2008; 93:e59] 1-gen-2008 Zadra, G.; Asselta, R.; Tenchini, M. L.; Castaman, G.; Seligsohn, U.; Mannucci, P. M.; Duga, S.
Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutations 1-gen-2008 Castaman, G.; Giacomelli, S. H.; Duga, S.; Rodeghiero, F.
State of the art of rare bleeding disorders database (RBDD) 1-gen-2008 Spreafico, M.; Menegatti, M.; Palla, R.; Garagiola, I.; Tagliabue, L.; Cairo, A.; Lavoretano, S.; Asselta, R.; Duga, S.; Mannucci, P. M.; Peyvandi, F.
Congenital hypofibrinogenemia : characterization of two missense mutations affecting fibrinogen assembly and secretion 1-gen-2008 Platè, M.; Asselta, R.; Spena, S.; Spreafico, M.; Fagoonee, S.; Peyvandi, F.; Tenchini, M. L.; Duga, S.
Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiency 1-gen-2009 Spena, S.; Asselta, R.; Caccia, S.; Rimoldi, V.; Giacomelli, S. H.; Tagliaferri, A.; Peyvandi, F.; Castaman, G.; Duga, S.
Mostrati risultati da 141 a 160 di 300
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