BARONIO, Manuela

BARONIO, Manuela  

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A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. 1-gen-2012 Lougaris, Vassilios; Gallizzi, R; Vitali, Massimiliano; Baronio, Manuela; Salpietro, A; Bergbreiter, A; Salzer, U; Badolato, Raffaele; Plebani, Alessandro
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 1-gen-2015 Lougaris, Vassilios; Faletra, Flavio; Lanzi, Gaetana; Vozzi, Diego; Marcuzzi, Annalisa; Valencic, Erica; Piscianz, Elisa; Bianco, Annamonica; Girardelli, Martina; Baronio, Manuela; Loganes, Claudia; Fasth, Anders; Salvini, Filippo; Trizzino, Antonino; Moratto, Daniele; Facchetti, Fabio; Giliani, Silvia Clara; Plebani, Alessandro; Tommasini, Alberto
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation. 1-gen-2014 Lougaris, Vassilios; Vitali, Massimiliano; Baronio, Manuela; Moratto, D; Tampella, Giacomo; Biasini, A; Badolato, Raffaele; Plebani, Alessandro
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency. 1-gen-2012 Lougaris, Vassilios; Baronio, Manuela; Vitali, Massimiliano; Tampella, Giacomo; Soresina, A; Badolato, Raffaele; Plebani, Alessandro
BAFF-R mutations in Good's syndrome. 1-gen-2014 Lougaris, Vassilios; Vitali, Massimiliano; Baronio, Manuela; Tampella, Giacomo; Plebani, Alessandro
Beta2 integrins are required for follicular helper T cell differentiation in humans 1-gen-2017 Gerosa, Jolanda; Lougaris, Vassilios; Baronio, Manuela; Plebani, Alessandro; Cicalese, Maria Pia; Fousteri, Georgia
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation. 1-gen-2014 Lougaris, Vassilios; Baronio, Manuela; Vitali, Massimiliano; Tampella, Giacomo; Cattalini, Marco; Tassone, L; Soresina, A; Badolato, Raffaele; Plebani, Alessandro
Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency 1-gen-2015 Gualdi, G; Lougaris, Vassilios; Baronio, Manuela; Vitali, Massimiliano; Tampella, Giacomo; Moratto, D; Tanghetti, P; Monari, P; CALZAVARA PINTON, Piergiacomo; Plebani, Alessandro
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis 1-gen-2023 Baronio, Manuela; Gazzurelli, Luisa; Rezzola, Sara; Rossi, Stefano; Tessarin, Giulio; Marinoni, Maddalena; Damiano, Annamaria Salpietro; Fiore, Michele; Moratto, Daniele; Chiarini, Marco; Badolato, Raffaele; Parolini, Silvia; Tabellini, Giovanna; Lougaris, Vassilios
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients 1-gen-2015 Lougaris, Vassilios; Baronio, Manuela; Masneri, Stefania; Lorenzini, Tiziana; Cattivelli, Kim; Tampella, Giacomo; Soresina, Annarosa; Moratto, Daniele; Plebani, Alessandro
CTLA-4 regulates human Natural Killer cell effector functions 1-gen-2018 Lougaris, Vassilios; Tabellini, Giovanna; Baronio, Manuela; Patrizi, Ornella; Gazzurelli, Luisa; Mitsuiki, Noriko; Pozzi, Maria Rosa; Grimbacher, Bodo; Parolini, Silvia; Plebani, Alessandro
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease 1-gen-2015 Lougaris, Vassilios; Tabellini, Giovanna; Vitali, Massimiliano; Baronio, Manuela; Patrizi, Ornella; Tampella, Giacomo; Biasini, Augusto; Moratto, Daniele; Parolini, Silvia; Plebani, Alessandro
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. 1-gen-2012 Lopez Herrera, G.; Tampella, Giacomo; Pan Hammarstrom, Q.; Herholz, P.; Trujillo Vargas, C. M.; Phadwalk, ; Simon, A. K.; Moutschen, M.; Etzioni, A.; Mory, A.; Srugo, I.; Melamed, D.; Hultenby, K.; Liu, C.; Baronio, Manuela; Vitali, Massimiliano; Philippet, P.; Dideberg, V.; Aghamohammadi, A.; Rezaei, N.; Enright, V.; Du, L.; Salzer, U.; Eibel, H.; Pfeifer, D.; Veelken, H.; Stauss, H.; Lougaris, Vassilios; Plebani, Alessandro; Gertz, E. M.; Schaffer, A. A.; Hammarstrom, L.; Grimbacher, B.
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease 1-gen-2016 Lougaris, Vassilios; Moratto, Daniele; Baronio, Manuela; Tampella, Giacomo; van der Meer, Jos W. M; Badolato, Raffaele; Fliegauf, Manfred; Plebani, Alessandro
Espansione di una rara popolazione linfocitaria con fenotipo CD8+CD28-CD11b- in pazienti sieropositivi per HIV. 1-gen-2001 Bonfanti, Carlo; Licenziati, Stefano; Baronio, Manuela; Bozzo, Luisa; Caruso, Arnaldo; Fiorentini, Simona
Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency. 1-gen-2011 Tampella, Giacomo; Baronio, Manuela; Vitali, Massimiliano; Soresina, A; Badolato, Raffaele; Giliani, Silvia Clara; Plebani, Alessandro; Lougaris, Vassilios
From Natural Killer Cell Receptor Discovery to Characterization of Natural Killer Cell Defects in Primary Immunodeficiencies 1-gen-2019 Tabellini, G.; Patrizi, O.; Dobbs, K.; Lougaris, V.; Baronio, M.; Coltrini, D.; Plebani, A.; Badolato, R.; Notarangelo, L. D.; Parolini, S.
HIV-1 matrix protein p17 increases the production of proinflammatory cytokines and counteracts IL-4 activity by binding to a cellular receptor. 1-gen-2002 DE FRANCESCO, Maria Antonia; Baronio, Manuela; Fiorentini, Simona; Signorini, C; Bonfanti, Carlo; Poiesi, C; Popovic, M; Grassi, M; Garrafa, Emirena Michela; Bozzo, L; Lewis, Gk; Licenziati, S; Gallo, Rc; Caruso, Arnaldo
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies 1-gen-2016 Lougaris, Vassilios; Baronio, Manuela; Moratto, Daniele; Cardinale, Fabio; Plebani, Alessandro
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay 1-gen-2018 Lougaris, Vassilios; Chou, Janet; Baronio, Manuela; Gazzurelli, Luisa; Lorenzini, Tiziana; Soresina, Annarosa; Moratto, Daniele; Badolato, Raffaele; Seleman, Michael; Bellettato, Massimo; Geha, Raif S; Plebani, Alessandro