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Titolo Data di pubblicazione Autore(i) File
Retrospective evaluation of dysfibrinogenaemic patients in a single centre: clinical features and laboratory findings 1-gen-2009 Santoro, C; Leporace, A; Biondo, F; Asselta, R; Duga, S; Menegatti, M; Platè, M; Mazzucconi, M
Molecular characterization of 9 genetic defects responsible for FV deficiency 1-gen-2009 Guella, I; Duga, S; Peyvandi, F; Mannucci, Pm; Asselta, R
Retrospective evaluation of dysifibrinogenemic patients at a single center: clinical features and laboratory findings 1-gen-2009 Santoro, C; Leporace, Ap; Biondo, F; Plate, M; Asselta, R; Peyvandi, F; Menegatti, M; Pignoloni, P; Duga, S; Foa, R; Mazzucconi, Mg
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 1-gen-2009 Asselta, R; Paraboschi, E; Solda, G; Dall’Osso, C; Gemmati, D; Zamboni, P; Benedetti, Md; D’Alfonso, S; Duga, S
Mutational screening of 25 unrelated FV-deficient patients from six countries 1-gen-2009 Guella, I.; Paraboschi, E.; Duga, S.; Peyvandi, F.; Gemmati, D.; Ciavarella, N.; Mannucci, P. M.; Asselta, R.
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 1-gen-2009 Solda, G; Paraboschi, Em; Gemmati, D; Zamboni, P; Duga, S; Asselta, R
Characterization of the genetic basis of FXI deficiency in fourteen unrelated patients 1-gen-2009 Rimoldi, V.; Guella, I.; Spena, S.; Ciavarella, N.; Peyvandi, F.; Asselta, R.; Mannucci, P. M.; Duga, S.
Association and functional analyses of MEF2A as a susceptibility gene for premature myocardial infarction and coronary artery disease 1-gen-2009 Guella, I.; Rimoldi, V.; Asselta, R.; Ardissino, D.; Francolini, M.; Martinelli, N.; Girelli, D.; Peyvandi, F.; Tubaro, M.; Merlini, P. A.; Mannucci, P. M.; Duga, S.
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants 1-gen-2009 Kathiresan, S.; Voight, B. F.; Purcell, S.; Musunuru, K.; Ardissino, D.; Mannucci, P. M.; Anand, S.; Engert, J. C.; Samani, N. J.; Schunkert, H.; Erdmann, J.; Reilly, M. P.; Rader, D. J.; Morgan, T.; Spertus, J. A.; Stoll, M.; Girelli, D.; Mckeown, P. P.; Patterson, C. C.; Siscovick, D. S.; O'Donnell, C. J.; Elosua, R.; Peltonen, L.; Salomaa, V.; Schwartz, S. M.; Melander, O.; Altshuler, D.; Ardissino, D.; Merlini, P. A.; Berzuini, C.; Bernardinelli, L.; Peyvandi, F.; Tubaro, M.; Celli, P.; Ferrario, M.; Fetiveau, R.; Marziliano, N.; Casari, G.; Galli, M.; Ribichini, F.; Rossi, M.; Bernardi, F.; Zonzin, P.; Piazza, A.; Mannucci, P. M.; Schwartz, S. M.; Siscovick, D. S.; Yee, J.; Friedlander, Y.; Elosua, R.; Marrugat, J.; Lucas, G.; Subirana, I.; Sala, J.; Ramos, R.; Kathiresan, S.; Meigs, J. B.; Williams, G.; Nathan, D. M.; Macrae, C. A.; O'Donnell, C. J.; Salomaa, V.; Havulinna, A. S.; Peltonen, L.; Melander, O.; Berglund, G.; Voight, B. F.; Kathiresan, S.; Hirschhorn, J. N.; Asselta, R.; Duga, S.; Spreafico, M.; Musunuru, K.; Daly, M. J.; Purcell, S.; Voight, B. F.; Purcell, S.; Nemesh, J.; Korn, J. M.; Mccarroll, S. A.; Schwartz, S. M.; Yee, J.; Kathiresan, S.; Lucas, G.; Subirana, I.; Elosua, R.; Surti, A.; Guiducci, C.; Gianniny, L.; Mirel, D.; Parkin, M.; Burtt, N.; Gabriel, S. B.; Samani, N. J.; Thompson, J. R.; Braund, P. S.; Wright, B. J.; Balmforth, A. J.; Ball, S. G.; Hall, A. S.; Trust Case Control Consortium, Wellcome; Schunkert, H.; Erdmann, J.; Linsel Nitschke, P.; Lieb, W.; Ziegler, A.; König, I.; Hengstenberg, C.; Fischer, M.; Stark, K.; Grosshennig, A.; Preuss, M.; Wichmann, H. E.; Schreiber, S.; Schunkert, H.; Samani, N. J.; Erdmann, J.; Ouwehand, W.; Hengstenberg, C.; Deloukas, P.; Scholz, M.; Cambien, F.; Reilly, M. P.; Li, M.; Chen, Z.; Wilensky, R.; Matthai, W.; Qasim, A.; Hakonarson, H. H.; Devaney, J.; Burnett, M. S.; Pichard, A. D.; Kent, K. M.; Satler, L.; Lindsay, J. M.; Waksman, W. R.; Knouff, C. W.; Waterworth, D. M.; Walker, M. C.; Mooser, V.; Epstein, S. E.; Rader, D. J.; Scheffold, T.; Berger, K.; Stoll, M.; Huge, A.; Girelli, D.; Martinelli, N.; Olivieri, O.; Corrocher, R.; Morgan, T.; Spertus, J. A.; Mckeown, P.; Patterson, C. C.; Schunkert, H.; Erdmann, E.; Linsel Nitschke, P.; Lieb, W.; Ziegler, A.; König, I. R.; Hengstenberg, C.; Fischer, M.; Stark, K.; Grosshennig, A.; Preuss, M.; Wichmann, H. E.; Schreiber, S.; Hólm, H.; Thorleifsson, G.; Thorsteinsdottir, U.; Stefansson, K.; Engert, J. C.; Do, R.; Xie, C.; Anand, S.; Kathiresan, S.; Ardissino, D.; Mannucci, P. M.; Siscovick, D.; O'Donnell, C. J.; Samani, N. J.; Melander, O.; Elosua, R.; Peltonen, L.; Salomaa, V.; Schwartz, S. M.; Altshuler, D.
Factor XI deficiency 1-gen-2009 Duga, S.; Salomon, O.
RECURRENCE OF THE “DEEP-INTRONIC” FGG IVS6-320A>T MUTATION CAUSING QUANTITATIVE FIBRINOGEN DEFICIENCY IN THE ITALIAN POPULATION OF VENETO 1-gen-2009 Platè, M; Duga, S; Castaman, G; Rodeghiero, F; Asselta, R
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.
Tau and alpha-synuclein and genetic susceptibility to Parkinson Disease in the Italian population 1-gen-2010 Guella, I; Trotta, L; Asselta, R; Solda', G; Zini, M; Zecchinelli, A; Pezzoli, G; Goldwurm, S; Duga, S
Role of the microRNA-183 family in the pathogenesis of hereditary nonsyndromic hearing loss in the Italian population 1-gen-2010 Soldà, G; Oldoni, F; Asselta, R; Primignani, P; Castorina, P; Radaelli, C; Coviello, D; Duga, S
hUPF1 and hUPF2 knockdown by RNA interference in HepG2 cells as a model to study nonsense-mediated mRNA decay modulation of coagulation-gene expression 1-gen-2010 Platè, M; Rimoldi, V; Duga, S; Asselta, R
The double-faced association of the PRKCA gene with multiple sclerosis 1-gen-2010 Paraboschi, E; Solda', G; Rimoldi, V; Dall’Osso, C; Anelli, G; Gemmati, D; Zamboni, P; Benedetti, Md; D’Alfonso, S; Duga, S; Asselta, R
Premature termination codon mutations in the von Willebrand factor gene are associated with allele-specific and position-dependent mRNA decay 1-gen-2010 Platè, M; Duga, S; Baronciani, L; LA MARCA, S; Rubini, V; Mannucci, Pm; Federici, Ab; Asselta, R
The association of factor V Leiden with myocardial infarction is replicated in 1880 patients with premature disease 1-gen-2010 Mannucci, P. M.; Asselta, R.; Duga, S.; Guella, I.; Spreafico, M.; Lotta, L. A.; Merlini, P. A.; Peyvandi, F.; Kathiresan, S.; Ardissino, D.
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA 1-gen-2010 Asselta, R; Rimoldi, V; Guella, I; Solda, G; De Cristofaro, R; Peyvandi, F; Duga, S.
Effects of PCSK9 genetic variants on plasma LDL cholesterol levels and risk of premature myocardial infarction in the Italian population 1-gen-2010 Guella, I.; Asselta, R.; Ardissino, D.; Merlini, P. A.; Peyvandi, F.; Kathiresan, S.; Mannucci, P. M.; Tubaro, M.; Duga, S.
Mostrati risultati da 161 a 180 di 300
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