LORENZINI, TIZIANA
LORENZINI, TIZIANA
Dipartimento di Scienze Cliniche e Sperimentali
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 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
Autosomal-dominant hyper-IgE syndrome is associated with appearance of infections early in life and/or neonatal rash: Evidence from the Italian cohort of 61 patients with elevated IgE
2019-01-01 Lorenzini, T.; Giacomelli, M.; Scomodon, O.; Cortesi, M.; Rivellini, V.; Dotta, L.; Soresina, A.; Dellepiane, R. M.; Carrabba, M.; Cossu, F.; Cancrini, C.; Specchia, F.; Giardino, G.; Pignata, C.; Plebani, A.; Pietrogrande, M. C.; Badolato, R.
Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study
2019-01-01 Lougaris, V.; Sorlini, A.; Monfredini, Chiara; Ingrasciotta, Giulia; Caravaggio, A.; Lorenzini, T.; Baronio, M.; Cattalini, M.; Meini, A.; Ruggeri, L.; Salpietro, A.; Pilotta, A.; Grazzani, Livia; Prandi, Elena; Felappi, B.; Gualdi, G.; Fabiano, A.; Fuoti, M.; Ravelli, A.; Villanacci, V.; Soresina, A.; Badolato, R.; Plebani, A.
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients
2015-01-01 Lougaris, Vassilios; Baronio, Manuela; Masneri, Stefania; Lorenzini, Tiziana; Cattivelli, Kim; Tampella, Giacomo; Soresina, Annarosa; Moratto, Daniele; Plebani, Alessandro
Corrigendum to: “Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET)” [Vaccine 36 (2018) Pages 3541–3542](S0264410X1830121X)(10.1016/j.vaccine.2018.01.061)
2018-01-01 Martire, B.; Azzari, C.; Badolato, R.; Canessa, C.; Cirillo, E.; Gallo, V.; Graziani, S.; Lorenzini, T.; Milito, C.; Panza, R.; Moschese, V.
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity.
2019-01-01 Lougaris, V; Moratto, D; Baronio, M; Lorenzini, T; Rossi, S; Gazzurelli, L; Bondioni, Mp; Plebani, A.
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay
2018-01-01 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
Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency
2018-01-01 Lougaris, Vassilios; Lanzi, Gaetana; Baronio, Manuela; Gazzurelli, Luisa; Vairo, Donatella; Lorenzini, Tiziana; Badolato, Raffaele; Notarangelo, Lucia Dora; Boschi, Andrea; Moratto, Daniele; Plebani, Alessandro
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome
2016-01-01 Lougaris, Vassilios; Facchini, Elena; Baronio, Manuela; Lorenzini, Tiziana; Moratto, Daniele; Specchia, Fernando; Plebani, Alessandro
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions
2016-01-01 Giacomelli, Mauro Simone; Kumar, Rajesh; Soresina, Annarosa; Tamassia, Nicola; Lorenzini, Tiziana; Moratto, Daniele; Gasperini, Sara; Cassatella, Marco; Plebani, Alessandro; Lougaris, Vassilios; Badolato, Raffaele
STAT mutations as program switchers: Turning primary immunodeficiencies into autoimmune diseases
2017-01-01 Lorenzini, Tiziana; Dotta, Laura; Giacomelli, Mauro; Vairo, Donatella; Badolato, Raffaele
Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET)
2018-01-01 Martire, Baldassarre; Azzari, Chiara; Badolato, Raffaele; Canessa, Clementina; Cirillo, Emilia; Gallo, Vera; Graziani, Simona; Lorenzini, Tiziana; Milito, Cinzia; Panza, Raffaella; Moschese, Viviana
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 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 | |
| Autosomal-dominant hyper-IgE syndrome is associated with appearance of infections early in life and/or neonatal rash: Evidence from the Italian cohort of 61 patients with elevated IgE | 1-gen-2019 | Lorenzini, T.; Giacomelli, M.; Scomodon, O.; Cortesi, M.; Rivellini, V.; Dotta, L.; Soresina, A.; Dellepiane, R. M.; Carrabba, M.; Cossu, F.; Cancrini, C.; Specchia, F.; Giardino, G.; Pignata, C.; Plebani, A.; Pietrogrande, M. C.; Badolato, R. | |
| Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study | 1-gen-2019 | Lougaris, V.; Sorlini, A.; Monfredini, Chiara; Ingrasciotta, Giulia; Caravaggio, A.; Lorenzini, T.; Baronio, M.; Cattalini, M.; Meini, A.; Ruggeri, L.; Salpietro, A.; Pilotta, A.; Grazzani, Livia; Prandi, Elena; Felappi, B.; Gualdi, G.; Fabiano, A.; Fuoti, M.; Ravelli, A.; Villanacci, V.; Soresina, A.; Badolato, R.; Plebani, A. | |
| 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 | |
| Corrigendum to: “Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET)” [Vaccine 36 (2018) Pages 3541–3542](S0264410X1830121X)(10.1016/j.vaccine.2018.01.061) | 1-gen-2018 | Martire, B.; Azzari, C.; Badolato, R.; Canessa, C.; Cirillo, E.; Gallo, V.; Graziani, S.; Lorenzini, T.; Milito, C.; Panza, R.; Moschese, V. | |
| Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity. | 1-gen-2019 | Lougaris, V; Moratto, D; Baronio, M; Lorenzini, T; Rossi, S; Gazzurelli, L; Bondioni, Mp; Plebani, A. | |
| 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 | |
| Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency | 1-gen-2018 | Lougaris, Vassilios; Lanzi, Gaetana; Baronio, Manuela; Gazzurelli, Luisa; Vairo, Donatella; Lorenzini, Tiziana; Badolato, Raffaele; Notarangelo, Lucia Dora; Boschi, Andrea; Moratto, Daniele; Plebani, Alessandro | |
| Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome | 1-gen-2016 | Lougaris, Vassilios; Facchini, Elena; Baronio, Manuela; Lorenzini, Tiziana; Moratto, Daniele; Specchia, Fernando; Plebani, Alessandro | |
| Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions | 1-gen-2016 | Giacomelli, Mauro Simone; Kumar, Rajesh; Soresina, Annarosa; Tamassia, Nicola; Lorenzini, Tiziana; Moratto, Daniele; Gasperini, Sara; Cassatella, Marco; Plebani, Alessandro; Lougaris, Vassilios; Badolato, Raffaele | |
| STAT mutations as program switchers: Turning primary immunodeficiencies into autoimmune diseases | 1-gen-2017 | Lorenzini, Tiziana; Dotta, Laura; Giacomelli, Mauro; Vairo, Donatella; Badolato, Raffaele | |
| Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET) | 1-gen-2018 | Martire, Baldassarre; Azzari, Chiara; Badolato, Raffaele; Canessa, Clementina; Cirillo, Emilia; Gallo, Vera; Graziani, Simona; Lorenzini, Tiziana; Milito, Cinzia; Panza, Raffaella; Moschese, Viviana |