PLEBANI, Alessandro
PLEBANI, Alessandro
A case of lymphoproliferative disease presenting with a clinical and immunological phenotype of common variable immunodeficiency.
2002-01-01 Soresina, A; Insalaco, A; Giliani, Silvia Clara; Castagna, M; Forino, C; Arrighetti, A; Lougaris, V; Plebani, Alessandro
A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling “Nijmegen breakage syndrome” phenotype
2007-01-01 Berardinelli, F; DI MASI, A; Salvatore, M; Banerjee, S; Myung, K; DE VILLARTY, Jp; Soresina, A; Plebani, Alessandro; Taruscio, D; Tanzarella, C; Antoccia, A.
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
A comparison of secretory antibodies in breast-fed and formula-fed infants over the first six months of life.
1992-01-01 Avanzini, M. A.; Plebani, Alessandro; Monafo, V.; Pasinetti, G.; Teani, M.; Colombo, A.; Mellander, L.; Carlsson, B.; Hanson, L. A.; Ugazio, Alberto Giovanni; Burgio, G. R.
A CVID-associated variant in the ciliogenesis protein CCDC28B disrupts immune synapse assembly
2021-01-01 Capitani, N.; Onnis, A.; Finetti, F.; Cassioli, C.; Plebani, A.; Brunetti, J.; Troilo, A.; D'Elios, S.; Baronio, M.; Gazzurelli, L.; Della Bella, C.; Billadeau, D. D.; D'Elios, M. M.; Lougaris, V.; Baldari, C. T.
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
A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy.
2018-01-01 Lougaris, V; Baronio, M; Gazzurelli, L; Lorenzini, T; Fuoti, M; Moratto, D; Bozzola, A; Ricci, C; Bondioni, Mp; Ravelli, A; Villanacci, V; Plebani, A.
A homozygous CARD9 mutation in a family with susceptibility to fungal infections.
2009-01-01 Glocker, Eo; Hennigs, A; Nabavi, M; Schaffer, Aa; Woellner, C; Salzer, U; Pfeifer, D; Veelken, H; Warnatz, K; Tahami, F; Jamal, S; Manguiat, A; Rezaei, N; Amirzargar, Aa; Plebani, Alessandro; Hannesschlager, N; Gross, O; Ruland, J; Grimbacher, B.
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency
2019-01-01 Lougaris, Vassilios; Chou, Janet; Beano, Abdallah; Wallace, Jacqueline G.; Baronio, Manuela; Gazzurelli, Luisa; Lorenzini, Tiziana; Moratto, Daniele; Tabellini, Giovanna; Parolini, Silvia; Seleman, Michael; Stafstrom, Kelsey; Xu, Haiming; Harris, Chad; Geha, Raif S.; Plebani, Alessandro
A new immunoperoxidase assay for lolium perenne-specific IgE in serum based on the biotin/avidin system (BAS).
1984-01-01 Plebani, Alessandro; Notarangelo, Luigi Daniele; Monafo, V.; Nespoli, L.; Ugazio, Alberto Giovanni
A novel activation-induced cytidine deaminase gene mutation in a Tunisian family with hyper IgM syndrome.
2004-01-01 Fiorini, Claudia; Jilani, S; Losi, Claretta Gioia; Silini, Antonietta; Giliani, Silvia Clara; Ferrari, S; Notarangelo, Luigi Daniele; Plebani, Alessandro; Sfar, T; Helal, A.
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
A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG
2007-01-01 Plebani, Alessandro; Lougaris, Vassilios; Soresina, A; Meini, A; Zunino, F; Losi, Cg; Gatta, R; Cattaneo, G; Nespoli, L; Marinoni, M; Capolunghi, F; Vivarelli, M; Quinti, I; Carsetti, R.
A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1)
2019-01-01 Lougaris, Vassilios; Baronio, Manuela; Moratto, Daniele; Tampella, Giacomo; Gazzurelli, Luisa; Facchetti, Mattia; Martire, Baldassarre; Cardinale, Fabio; Lanzarotto, Francesco; Bondioni, Maria Pia; Villanacci, Vincenzo; Grimbacher, Bodo; Plebani, Alessandro
A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP
2012-01-01 Lanzi, Gaetana; Moratto, Daniele; Vairo, Donatella; Masneri, Stefania; Delmonte, Ottavia; Paganini, Tiziana; Parolini, Silvia; Tabellini, Giovanna; Mazza, Cinzia; Savoldi, Gianfranco; Montin, Davide; Martino, Silvana; Tovo, Pierangelo; Pessach, Itai M.; Massaad, Michel J.; Ramesh, Narayanaswamy; Porta, Fulvio; Plebani, Alessandro; Notarangelo, Luigi D.; Geha, Raif S.; Giliani, Silvia Clara
A possible role for B cells in COVID-19? Lesson from patients with agammaglobulinemia
2020-01-01 Quinti, Isabella; Lougaris, Vassilios; Milito, Cinzia; Cinetto, Francesco; Pecoraro, Antonio; Mezzaroma, Ivano; Mastroianni, Claudio Maria; Turriziani, Ombretta; Bondioni, Maria Pia; Filippini, Matteo; Soresina, Annarosa; Spadaro, Giuseppe; Agostini, Carlo; Carsetti, Rita; Plebani, Alessandro
A prospective study on children with initial diagnosis of transient hypogammaglobulinemia of infancy: results from the Italian Primari Immunodeficiency Network.
2008-01-01 Moschese, V; Graziani, S; Avanzini, Ma; Carsetti, R; Marconi, M; LA ROCCA, M; Chini, L; Pignata, C; Soresina, A; Consolini, R; Bossi, G; Trizzino, A; Martino, S; Cardinale, F; Bertolini, P; Marseglia, Gl; Zecca, M; DI CESARE, S; Quinti, I; Rondelli, R; Pietrogrande, Mc; Rossi, P; Plebani, Alessandro; WITHIN THE, Ipinet
A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia
2012-01-01 Zannolli, R; Buoni, S; Betti, G; Salvucci, S; Plebani, Alessandro; Soresina, A; Pietrogrande, Mc; Martino, S; Leuzzi, V; Finocchi, A; Micheli, R; Rossi, Ln; Brusco, A; Misiani, F; Fois, A; Hayek, J; Kelly, C; Chessa, L.
A video densitometric analysis of viral burden and follicular dendritic cell damage in lymph nodes in the latency phase of HIV infection
2000-01-01 Zannini, C; Favre, A; Ciccone, E; Plebani, Alessandro; Duse, M; Grossi, Ce; Pesce, C.
Acquired immune deficiency syndrome in childhood: impaired production of interleukin-2 by HIV (LAV/HTLV III) infected patients.
1987-01-01 Maccario, R.; Aricò, M.; Ugazio, Alberto Giovanni; Plebani, Alessandro; Montagna, D.; Avanzini, A.; Marseglia, G.; Caselli, D.; Burgio, G. R.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A case of lymphoproliferative disease presenting with a clinical and immunological phenotype of common variable immunodeficiency. | 1-gen-2002 | Soresina, A; Insalaco, A; Giliani, Silvia Clara; Castagna, M; Forino, C; Arrighetti, A; Lougaris, V; Plebani, Alessandro | |
| A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling “Nijmegen breakage syndrome” phenotype | 1-gen-2007 | Berardinelli, F; DI MASI, A; Salvatore, M; Banerjee, S; Myung, K; DE VILLARTY, Jp; Soresina, A; Plebani, Alessandro; Taruscio, D; Tanzarella, C; Antoccia, A. | |
| 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 | |
| A comparison of secretory antibodies in breast-fed and formula-fed infants over the first six months of life. | 1-gen-1992 | Avanzini, M. A.; Plebani, Alessandro; Monafo, V.; Pasinetti, G.; Teani, M.; Colombo, A.; Mellander, L.; Carlsson, B.; Hanson, L. A.; Ugazio, Alberto Giovanni; Burgio, G. R. | |
| A CVID-associated variant in the ciliogenesis protein CCDC28B disrupts immune synapse assembly | 1-gen-2021 | Capitani, N.; Onnis, A.; Finetti, F.; Cassioli, C.; Plebani, A.; Brunetti, J.; Troilo, A.; D'Elios, S.; Baronio, M.; Gazzurelli, L.; Della Bella, C.; Billadeau, D. D.; D'Elios, M. M.; Lougaris, V.; Baldari, C. T. | |
| 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 | |
| A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy. | 1-gen-2018 | Lougaris, V; Baronio, M; Gazzurelli, L; Lorenzini, T; Fuoti, M; Moratto, D; Bozzola, A; Ricci, C; Bondioni, Mp; Ravelli, A; Villanacci, V; Plebani, A. | |
| A homozygous CARD9 mutation in a family with susceptibility to fungal infections. | 1-gen-2009 | Glocker, Eo; Hennigs, A; Nabavi, M; Schaffer, Aa; Woellner, C; Salzer, U; Pfeifer, D; Veelken, H; Warnatz, K; Tahami, F; Jamal, S; Manguiat, A; Rezaei, N; Amirzargar, Aa; Plebani, Alessandro; Hannesschlager, N; Gross, O; Ruland, J; Grimbacher, B. | |
| A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency | 1-gen-2019 | Lougaris, Vassilios; Chou, Janet; Beano, Abdallah; Wallace, Jacqueline G.; Baronio, Manuela; Gazzurelli, Luisa; Lorenzini, Tiziana; Moratto, Daniele; Tabellini, Giovanna; Parolini, Silvia; Seleman, Michael; Stafstrom, Kelsey; Xu, Haiming; Harris, Chad; Geha, Raif S.; Plebani, Alessandro | |
| A new immunoperoxidase assay for lolium perenne-specific IgE in serum based on the biotin/avidin system (BAS). | 1-gen-1984 | Plebani, Alessandro; Notarangelo, Luigi Daniele; Monafo, V.; Nespoli, L.; Ugazio, Alberto Giovanni | |
| A novel activation-induced cytidine deaminase gene mutation in a Tunisian family with hyper IgM syndrome. | 1-gen-2004 | Fiorini, Claudia; Jilani, S; Losi, Claretta Gioia; Silini, Antonietta; Giliani, Silvia Clara; Ferrari, S; Notarangelo, Luigi Daniele; Plebani, Alessandro; Sfar, T; Helal, A. | |
| 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 | |
| A novel immunodeficiency characterized by the exclusive presence of transitional B cells unresponsive to CpG | 1-gen-2007 | Plebani, Alessandro; Lougaris, Vassilios; Soresina, A; Meini, A; Zunino, F; Losi, Cg; Gatta, R; Cattaneo, G; Nespoli, L; Marinoni, M; Capolunghi, F; Vivarelli, M; Quinti, I; Carsetti, R. | |
| A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1) | 1-gen-2019 | Lougaris, Vassilios; Baronio, Manuela; Moratto, Daniele; Tampella, Giacomo; Gazzurelli, Luisa; Facchetti, Mattia; Martire, Baldassarre; Cardinale, Fabio; Lanzarotto, Francesco; Bondioni, Maria Pia; Villanacci, Vincenzo; Grimbacher, Bodo; Plebani, Alessandro | |
| A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP | 1-gen-2012 | Lanzi, Gaetana; Moratto, Daniele; Vairo, Donatella; Masneri, Stefania; Delmonte, Ottavia; Paganini, Tiziana; Parolini, Silvia; Tabellini, Giovanna; Mazza, Cinzia; Savoldi, Gianfranco; Montin, Davide; Martino, Silvana; Tovo, Pierangelo; Pessach, Itai M.; Massaad, Michel J.; Ramesh, Narayanaswamy; Porta, Fulvio; Plebani, Alessandro; Notarangelo, Luigi D.; Geha, Raif S.; Giliani, Silvia Clara | |
| A possible role for B cells in COVID-19? Lesson from patients with agammaglobulinemia | 1-gen-2020 | Quinti, Isabella; Lougaris, Vassilios; Milito, Cinzia; Cinetto, Francesco; Pecoraro, Antonio; Mezzaroma, Ivano; Mastroianni, Claudio Maria; Turriziani, Ombretta; Bondioni, Maria Pia; Filippini, Matteo; Soresina, Annarosa; Spadaro, Giuseppe; Agostini, Carlo; Carsetti, Rita; Plebani, Alessandro | |
| A prospective study on children with initial diagnosis of transient hypogammaglobulinemia of infancy: results from the Italian Primari Immunodeficiency Network. | 1-gen-2008 | Moschese, V; Graziani, S; Avanzini, Ma; Carsetti, R; Marconi, M; LA ROCCA, M; Chini, L; Pignata, C; Soresina, A; Consolini, R; Bossi, G; Trizzino, A; Martino, S; Cardinale, F; Bertolini, P; Marseglia, Gl; Zecca, M; DI CESARE, S; Quinti, I; Rondelli, R; Pietrogrande, Mc; Rossi, P; Plebani, Alessandro; WITHIN THE, Ipinet | |
| A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia | 1-gen-2012 | Zannolli, R; Buoni, S; Betti, G; Salvucci, S; Plebani, Alessandro; Soresina, A; Pietrogrande, Mc; Martino, S; Leuzzi, V; Finocchi, A; Micheli, R; Rossi, Ln; Brusco, A; Misiani, F; Fois, A; Hayek, J; Kelly, C; Chessa, L. | |
| A video densitometric analysis of viral burden and follicular dendritic cell damage in lymph nodes in the latency phase of HIV infection | 1-gen-2000 | Zannini, C; Favre, A; Ciccone, E; Plebani, Alessandro; Duse, M; Grossi, Ce; Pesce, C. | |
| Acquired immune deficiency syndrome in childhood: impaired production of interleukin-2 by HIV (LAV/HTLV III) infected patients. | 1-gen-1987 | Maccario, R.; Aricò, M.; Ugazio, Alberto Giovanni; Plebani, Alessandro; Montagna, D.; Avanzini, A.; Marseglia, G.; Caselli, D.; Burgio, G. R. |