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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
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 |
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Opzioni
Scopri
Tipologia
- 1 Contributo su Rivista 338
- 1 Contributo su Rivista::1.1 Arti... 322
- 1 Contributo su Rivista::1.5 Abst... 16
Data di pubblicazione
- 2020 - 2024 31
- 2010 - 2019 130
- 2000 - 2009 102
- 1990 - 1999 44
- 1980 - 1989 28
- 1978 - 1979 3
Editore
- Elsevier Science Incorporated / N... 8
- American Association of Immunolog... 5
- American Society of Hematology:19... 5
- Lippincott, Williams & Wilkins:53... 5
- Cell Press:1100 Massachusetts Ave... 4
- Springer Verlag Germany:Tiergarte... 4
- Mosby Year Book Incorporated:6277... 3
- Ospedaletto : Pacini Editore 3
- Plenum Press:Book Customer Servic... 3
- American Society for Clinical Inv... 2
Rivista
- CLINICAL IMMUNOLOGY 37
- JOURNAL OF CLINICAL IMMUNOLOGY 25
- JOURNAL OF ALLERGY AND CLINICAL I... 21
- BLOOD 14
- JOURNAL OF IMMUNOLOGY 10
- CLINICAL AND EXPERIMENTAL IMMUNOLOGY 8
- FRONTIERS IN IMMUNOLOGY 6
- EUROPEAN JOURNAL OF PEDIATRICS 5
- JOURNAL OF ALLERGY AND CLINICAL I... 5
- THE ITALIAN JOURNAL OF PEDIATRICS 5
Keyword
- Immunology 23
- Immunology and Allergy 23
- common variable immunodeficiency 17
- Humans 13
- B cells 10
- agammaglobulinemia 9
- Male 9
- Child 8
- Female 7
- immunodeficiency 7
Lingua
- eng 327
- ita 3
- fre 1
Accesso al fulltext
- no fulltext 313
- open 10
- reserved 8
- restricted 7