Sfoglia per Autore
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity.
2012-01-01 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.
The significance of duodenal mucosa atrophy in patients with common variable immunodeficiency: a clinical and histopatological study
2012-01-01 Biagi, F; Bianchi, Pi; Zilli, A; Marchese, A; Luinetti, O; Lougaris, Vassilios; Plebani, Alessandro; Villanacci, V; Corazza, G. R.
Expansion of somatically reverted memory CD8+ T cells in X-linked lymphoproliferative disease is due to selective pressure from Epstein Barr virus.
2012-01-01 Palendira, U; Low, C; Bell, Ai; Ma, Cs; Abbott, Rjm; Phan, Tg; Riminton, Ds; Choo, S; Smart, Jm; Lougaris, Vassilios; Giliani, Silvia Clara; Buckley, Rh; Grimbacher, B; Alvaro, F; Klion, Ad; Nichols, Ke; Adelstein, S; Rickinson, Ab; Tangye, Sg
ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID)
2012-01-01 Lougaris, Vassilios; Baronio, M; Vitali, M; Masneri, Stefania; Cattivelli, K; Folsi, V; Tampella, G; Moratto, Daniele; Soresina, A; Badolato, Raffaele; Giliani, Silvia Clara; Plebani, Alessandro
Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors.
2012-01-01 Kreuzaler, M; Rauch, M; Salzer, U; Birmelin, J; Rizzi, M; Grimbacher, B; Plebani, Alessandro; Lougaris, Vassilios; Quinti, I; Thon, V; Litzman, J; Schlesier, M; Warnatz, K; Thiel, J; Rolink, Ag; Eibel, H.
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency.
2012-01-01 Lougaris, Vassilios; Baronio, Manuela; Vitali, Massimiliano; Tampella, Giacomo; Soresina, A; Badolato, Raffaele; Plebani, Alessandro
GENETIC ANALYSIS OF THE TNFRSF13B GENE IN A LARGE ITALIAN CVID COHORT
2012-01-01 Lougaris, Vassilios; Vitali, M; Baronio, M; Tampella, G; Bergbreiter, A; Salzer, U; Soresina, A; Badolato, Raffaele; Giliani, Silvia Clara; Plebani, Alessandro
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family.
2012-01-01 Lougaris, Vassilios; Gallizzi, R; Vitali, Massimiliano; Baronio, Manuela; Salpietro, A; Bergbreiter, A; Salzer, U; Badolato, Raffaele; Plebani, Alessandro
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients.
2013-01-01 Wong, Gk; Goldacker, S; Winterhalter, C; Grimbacher, B; Chapel, H; Lucas, M; Alecsandru, D; Mcewen, D; Quinti, I; Martini, H; Schmidt, Re; Ernst, D; Espanol, T; Vidaller, A; Carbone, J; Fernandez Cruz, E; Lougaris, Vassilios; Plebani, Alessandro; Kutukculer, N; Gonzalez Granado, Li; Contreras, R; Kiani Alikhan, S; Ibrahim, Ma; Litzman, J; Jones, A; Gaspar, Hb; Hammarstrom, L; Baumann, U; Warnatz, K; Huissoon, Ap; Clinical Working Party of the European Society for, Immunodeficiencies
BAFF-R mutations in Good's syndrome.
2014-01-01 Lougaris, Vassilios; Vitali, Massimiliano; Baronio, Manuela; Tampella, Giacomo; Plebani, Alessandro
Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis.
2014-01-01 Sic, H; Kraus, H; Madl, J; Flittner, Ka; von Münchow, Al; Pieper, K; Rizzi, M; Kienzler, Ak; Ayata, K; Rauer, S; Kleuser, B; Salzer, U; Burger, M; Zirlik, K; Lougaris, Vassilios; Plebani, Alessandro; Römer, W; Loeffler, C; Scaramuzza, S; Villa, A; Noguchi, E; Grimbacher, B; Eibel, H.
CONGENITAL CYSTIC LUNG DISEASE: PRENATAL ULTRASOUND AND POSTNATAL MULTIDETECTOR COMPUTER TOMOGRAPHY EVALUATION. CORRELATION WITH SURGICAL AND PATHOLOGICAL DATA
2014-01-01 Bondioni, Maria Pia; Diego, Gatta; Lougaris, Vassilios; Nicoletta, Palai; Marino, Signorelli; Silvia, Michelini; Giuseppe Di, Gaetano; Paola, Tessitore; Lorella, Mascaro; Andrea, Tironi; Giovanni, Boroni; Maroldi, Roberto; Alberti, Daniele
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation.
2014-01-01 Lougaris, Vassilios; Vitali, Massimiliano; Baronio, Manuela; Moratto, D; Tampella, Giacomo; Biasini, A; Badolato, Raffaele; Plebani, Alessandro
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation.
2014-01-01 Lougaris, Vassilios; Baronio, Manuela; Vitali, Massimiliano; Tampella, Giacomo; Cattalini, Marco; Tassone, L; Soresina, A; Badolato, Raffaele; Plebani, Alessandro
Allergen immunotherapy, routes of administration and cytokine networks: An update
2014-01-01 Cuppari, Caterina; Leonardi, Salvatore; Manti, Sara; Filippelli, Martina; Alterio, Tommaso; Spicuzza, Lucia; Rigoli, Luciana; Arrigo, Teresa; Lougaris, Vassilios; Salpietro, Carmelo
A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency
2014-01-01 Kathrin, Pieper; Marta, Rizzi; Matthaios, Speletas; Cristian R., Smulski; Heiko, Sic; Helene, Kraus; Ulrich, Salzer; Gina J., Fiala; Wolfgang W., Schamel; Lougaris, Vassilios; Plebani, Alessandro; Lennart, Hammarstrom; Mike, Recher; Anastasios E., Germenis; Bodo, Grimbacher; Klaus, Warnatz; Antonius G., Rolink; Pascal, Schneider; Luigi D., Notarangelo; Hermann, Eibel
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a.
2014-01-01 Khalili, A; Plebani, Alessandro; Vitali, Massimiliano; Abolhassani, H; Lougaris, Vassilios; Mirminachi, B; Rezaei, N; Aghamohammadi, A.
Expansion of CCR4+ activated T cells is associated with memory B cell reduction in DOCK8-deficient patients.
2014-01-01 Caracciolo, S; Moratto, D; Giacomelli, M; Negri, S; Lougaris, Vassilios; Porta, F; Pajno, G; Salpietro, A; Montin, D; Dinwiddie, Dl; Kingsmore, Sf; Plebani, Alessandro; Badolato, Raffaele
Congenital cystic lung disease: prenatal ultrasound and postnatal multidetector computer tomography evaluation. Correlation with surgical and pathological data
2014-01-01 Bondioni, Maria Pia; Gatta, D; Lougaris, Vassilios; Palai, N; Signorelli, M; Michelini, S; Di Gaetano, G; Tessitore, Paola; Mascaro, L; Tironi, A; Boroni, G; Maroldi, Roberto; Alberti, Daniele
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity
2014-01-01 Giagulli, Cinzia; Caccuri, Francesca; Cignarella, Francesca; Lougaris, Vassilios; Martorelli, D; Bugatti, Antonella; Rusnati, Marco; Dolcetti, R; Vitali, Massimiliano; Plebani, Alessandro; Fiorentini, Simona; Caruso, Arnaldo
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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. | |
| The significance of duodenal mucosa atrophy in patients with common variable immunodeficiency: a clinical and histopatological study | 1-gen-2012 | Biagi, F; Bianchi, Pi; Zilli, A; Marchese, A; Luinetti, O; Lougaris, Vassilios; Plebani, Alessandro; Villanacci, V; Corazza, G. R. | |
| Expansion of somatically reverted memory CD8+ T cells in X-linked lymphoproliferative disease is due to selective pressure from Epstein Barr virus. | 1-gen-2012 | Palendira, U; Low, C; Bell, Ai; Ma, Cs; Abbott, Rjm; Phan, Tg; Riminton, Ds; Choo, S; Smart, Jm; Lougaris, Vassilios; Giliani, Silvia Clara; Buckley, Rh; Grimbacher, B; Alvaro, F; Klion, Ad; Nichols, Ke; Adelstein, S; Rickinson, Ab; Tangye, Sg | |
| ALTERED B AND T LYMPHOCYTE HOMEOSTASIS IN THE BONE MARROW AND THE PERIPHERY CORRELATES WITH CLINICAL FINDINGS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID) | 1-gen-2012 | Lougaris, Vassilios; Baronio, M; Vitali, M; Masneri, Stefania; Cattivelli, K; Folsi, V; Tampella, G; Moratto, Daniele; Soresina, A; Badolato, Raffaele; Giliani, Silvia Clara; Plebani, Alessandro | |
| Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors. | 1-gen-2012 | Kreuzaler, M; Rauch, M; Salzer, U; Birmelin, J; Rizzi, M; Grimbacher, B; Plebani, Alessandro; Lougaris, Vassilios; Quinti, I; Thon, V; Litzman, J; Schlesier, M; Warnatz, K; Thiel, J; Rolink, Ag; Eibel, H. | |
| 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 | |
| GENETIC ANALYSIS OF THE TNFRSF13B GENE IN A LARGE ITALIAN CVID COHORT | 1-gen-2012 | Lougaris, Vassilios; Vitali, M; Baronio, M; Tampella, G; Bergbreiter, A; Salzer, U; Soresina, A; Badolato, Raffaele; Giliani, Silvia Clara; Plebani, Alessandro | |
| 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 | |
| Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients. | 1-gen-2013 | Wong, Gk; Goldacker, S; Winterhalter, C; Grimbacher, B; Chapel, H; Lucas, M; Alecsandru, D; Mcewen, D; Quinti, I; Martini, H; Schmidt, Re; Ernst, D; Espanol, T; Vidaller, A; Carbone, J; Fernandez Cruz, E; Lougaris, Vassilios; Plebani, Alessandro; Kutukculer, N; Gonzalez Granado, Li; Contreras, R; Kiani Alikhan, S; Ibrahim, Ma; Litzman, J; Jones, A; Gaspar, Hb; Hammarstrom, L; Baumann, U; Warnatz, K; Huissoon, Ap; Clinical Working Party of the European Society for, Immunodeficiencies | |
| BAFF-R mutations in Good's syndrome. | 1-gen-2014 | Lougaris, Vassilios; Vitali, Massimiliano; Baronio, Manuela; Tampella, Giacomo; Plebani, Alessandro | |
| Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis. | 1-gen-2014 | Sic, H; Kraus, H; Madl, J; Flittner, Ka; von Münchow, Al; Pieper, K; Rizzi, M; Kienzler, Ak; Ayata, K; Rauer, S; Kleuser, B; Salzer, U; Burger, M; Zirlik, K; Lougaris, Vassilios; Plebani, Alessandro; Römer, W; Loeffler, C; Scaramuzza, S; Villa, A; Noguchi, E; Grimbacher, B; Eibel, H. | |
| CONGENITAL CYSTIC LUNG DISEASE: PRENATAL ULTRASOUND AND POSTNATAL MULTIDETECTOR COMPUTER TOMOGRAPHY EVALUATION. CORRELATION WITH SURGICAL AND PATHOLOGICAL DATA | 1-gen-2014 | Bondioni, Maria Pia; Diego, Gatta; Lougaris, Vassilios; Nicoletta, Palai; Marino, Signorelli; Silvia, Michelini; Giuseppe Di, Gaetano; Paola, Tessitore; Lorella, Mascaro; Andrea, Tironi; Giovanni, Boroni; Maroldi, Roberto; Alberti, Daniele | |
| 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 | |
| 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 | |
| Allergen immunotherapy, routes of administration and cytokine networks: An update | 1-gen-2014 | Cuppari, Caterina; Leonardi, Salvatore; Manti, Sara; Filippelli, Martina; Alterio, Tommaso; Spicuzza, Lucia; Rigoli, Luciana; Arrigo, Teresa; Lougaris, Vassilios; Salpietro, Carmelo | |
| A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency | 1-gen-2014 | Kathrin, Pieper; Marta, Rizzi; Matthaios, Speletas; Cristian R., Smulski; Heiko, Sic; Helene, Kraus; Ulrich, Salzer; Gina J., Fiala; Wolfgang W., Schamel; Lougaris, Vassilios; Plebani, Alessandro; Lennart, Hammarstrom; Mike, Recher; Anastasios E., Germenis; Bodo, Grimbacher; Klaus, Warnatz; Antonius G., Rolink; Pascal, Schneider; Luigi D., Notarangelo; Hermann, Eibel | |
| Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. | 1-gen-2014 | Khalili, A; Plebani, Alessandro; Vitali, Massimiliano; Abolhassani, H; Lougaris, Vassilios; Mirminachi, B; Rezaei, N; Aghamohammadi, A. | |
| Expansion of CCR4+ activated T cells is associated with memory B cell reduction in DOCK8-deficient patients. | 1-gen-2014 | Caracciolo, S; Moratto, D; Giacomelli, M; Negri, S; Lougaris, Vassilios; Porta, F; Pajno, G; Salpietro, A; Montin, D; Dinwiddie, Dl; Kingsmore, Sf; Plebani, Alessandro; Badolato, Raffaele | |
| Congenital cystic lung disease: prenatal ultrasound and postnatal multidetector computer tomography evaluation. Correlation with surgical and pathological data | 1-gen-2014 | Bondioni, Maria Pia; Gatta, D; Lougaris, Vassilios; Palai, N; Signorelli, M; Michelini, S; Di Gaetano, G; Tessitore, Paola; Mascaro, L; Tironi, A; Boroni, G; Maroldi, Roberto; Alberti, Daniele | |
| A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity | 1-gen-2014 | Giagulli, Cinzia; Caccuri, Francesca; Cignarella, Francesca; Lougaris, Vassilios; Martorelli, D; Bugatti, Antonella; Rusnati, Marco; Dolcetti, R; Vitali, Massimiliano; Plebani, Alessandro; Fiorentini, Simona; Caruso, Arnaldo |
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