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Titolo Data di pubblicazione Autore(i) File
Factor structure and reliability of the Italian adaptation of the Hypomania Check List-32, second revision (HCL-32-R2) 1-gen-2015 Fornaro, M; De Berardis, D; Mazza, M; Pino, M; Favarette, E; Bedani, F; Wieser, C; Indelicato, L; Paterno, Vf; Lo Monaco, F; Dugo, F; Ventriglio, A; Mungo, S; Selle, V; Valchera, A; Elassy, M; Martinotti, G; De Bartolomeis, A; Iasevoli, F; Tomasetti, C; Avvisati, L; Tartaglione, S; Perna, G; Cattaneo, Ci; Consoli, G; Romano, A; Del Debbio, A; Martino, M; D'Angelo, E; De Pasquale, C; Koshy, As; Angst, J
Factor structure of the Italian version of the Religious Fundamentalism Scale 1-gen-2013 Carlucci, Leonardo; Tommasi, Marco; Saggino, Aristide
The factor V (FV) gene ASP79HIS polymorphism modulates FV plasma levels and affects the activated protein C resistance phenotype in presence of the FV Leiden mutation 1-gen-2003 Bossone, A.; Cappucci, F.; D'Andrea, Giovanna; Brancaccio, V.; Cibelli, Giuseppe; Iannaccone, L.; Grandone, E.; Margaglione, Maurizio
Factor V Arg2074Cys: a novel missense mutation in the C2 domain of factor V. 1-gen-2002 Bossone, A; Dangelo, F; Santacroce, Rosa; DE LUCIA, D; Margaglione, Maurizio
Factor V Leiden is associated with repeated and recurrent unexplained fetal losses 1-gen-1997 Grandone, E; Margaglione, M; Colaizzo, D; D\'Anedda, M; Cappucci, G; Vecchione, G; Sciannamé, N; Pavone, G; DI MINNO, G
Factor V Leiden is associated with repeated and recurrent unexplained fetal losses. 1-gen-1997 Grandone, E; Margaglione, Maurizio; Colaizzo, D; D’Addedda, M; Cappucci, G; Vecchione, G; Sciannamé, N; Pavone, G; Di Minno, G.
Factor V Leiden is associated with repeated and recurrent unexplained fetal losses. Thromb Haemost 1997; 77: 822-824 1-gen-1997 Grandone, E; Margaglione, M; Colaizzo, D; D’Addedda, M; Cappucci, G; Vecchione, G; Sciannamé, N; Pavone, G; Di Minno, G
FACTOR V LEIDEN, C>T MTHFR POLYMORFISM AND GENETIC SUSCEPTIBILITY TO PREECLAMPSIA 1-gen-1997 Grandone, E; Margaglione, M; Colaizzo, D; Cappucci, G; Paladini, D; Martinelli, P; Montanaro, S; Pavone, G; DI MINNO, G
Factor V Leiden, C>T MTHFR polymorphism and genetic susceptibility to preeclampsia 1-gen-1997 Grandone, E; Margaglione, Maurizio; Colaizzo, D; Cappucci, G; Paladini, D; Martinelli, P; Montanaro, S; Pavone, G; Di Minno, G.
Factor V Leiden, C>T MTHFR polymorphism and genetic susceptibility to preeclampsia. Thromb Haemost 1997; 77: 1052-1054 1-gen-1997 Grandone, E; Margaglione, M; Colaizzo, D; Cappucci, G; Paladini, D; Martinelli, P; Montanaro, S; Pavone, G; Di Minno, G
Factor VII deficiency: a novel missense variant and genotype-phenotype correlation in patients from Southern Italy 1-gen-2017 Tiscia, G; Favuzzi, G; Chinni, E; Colaizzo, D; Fischetti, L; Intrieri, M; Margaglione, M; Grandone, E
Factor VII deficiency: a novel missense variant and genotype-phenotype correlation in patients from Southern Italy 1-gen-2017 Tiscia, MARIA GRAZIA; Favuzzi, G; Chinni, E; Colaizzo, D; Fischetti, L; Intrieri, M; Margaglione, M; Grandone, E.
Factor VII deficiency: a novel missense variant and genotype-phenotype correlation in patients from Southern Italy. 1-gen-2017 Tiscia, MARIA GRAZIA; Favuzzi, G; Chinni, E; Colaizzo, D; Fischetti, L; Intrieri, M; Margaglione, M; Grandone, E.
Factor VIII gene (F8) mutations as predictors of outcome in immune tolerance induction (ITI) of hemophilia A patients with high-responding inhibitors 1-gen-2009 Coppola, A.; Margaglione, Maurizio; Santagostino, E.; Rocino, A.; Grandone, E.; Mannucci, . P. M.; DI MINNO, G.; Santacroce, Rosa
Factor VIII gene (F8) mutations as predictors of outcome in immune tolerance induction of hemophilia A patients with high-responding inhibitors 1-gen-2009 Coppola, A; Margaglione, M; Santagostino, E; Rocino, A; Grandone, E; Mannucci, Pm; Di Minno, G; AICE PROFIT Study, Group
Factor XI deficiency: two novel mutations in asymptomatic Italian patients. 1-gen-2010 Tomaiuolo, M; Favuzzi, G; Cappucci, F; Pisanelli, D; Tiscia, Gl; Musto, P; Scaraggi, Fa; Cincione, RAFFAELE IVAN; Margaglione, Maurizio; Grandone, E.
Factor XI deficiency: two novelmutations in asymptomatic Italian patients 1-gen-2010 Tomaiuolo, M; Favuzzi, G; Cappucci, F; Pisanelli, D; Tiscia, Gl; Musto, P; Scaraggi, Fa; Cincione, Ri; Margaglione, M; Grandone, E
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 1-gen-2017 Tiscia, Giovanni L; Favuzzi, Giovanni; Lupone, Maria R; Cappucci, Filomena; Schiavulli, Michele; Mirabelli, Valentina; D'Andrea, Giovanna; Chinni, Elena; Giuliani, Nicola; Caliandro, Rocco; Grandone, Elvira
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 1-gen-2017 Tiscia, Giovanni L; Favuzzi, Giovanni; Lupone, Maria R; Cappucci, Filomena; Schiavulli, Michele; Mirabelli, Valentina; D'Andrea, Giovanna; Chinni, Elena; Giuliani, Nicola; Caliandro, Rocco; Grandone, Elvira
Factor xiii val34Leu polymorphism and risk of deep vein thrombosis. 1-gen-2000 Margaglione, Maurizio; Bossone, M; Brancaccio, V; Ciampa, A; Di Minno, G.
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