MORATTO, Daniele
MORATTO, Daniele
Dipartimento di Medicina Molecolare e Traslazionale
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 distinct human cell type expressing MHCII and RORγt with dual characteristics of dendritic cells and type 3 innate lymphoid cells
2023-01-01 Ulezko Antonova, Alina; Lonardi, Silvia; Monti, Matilde; Missale, Francesco; Fan, Changxu; Coates, Matthew L; Bugatti, Mattia; Jaeger, Natalia; Fernandes Rodrigues, Patrick; Brioschi, Simone; Trsan, Tihana; Fachi, José L; Nguyen, Khai M; Nunley, Ryan M; Moratto, Daniele; Zini, Stefania; Kong, Lingjia; Deguine, Jacques; Peeples, Mark E; Xavier, Ramnik J; Clatworthy, Menna R; Wang, Ting; Cella, Marina; Vermi, William; Colonna, Marco
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 novel EP300 mutation associated with Rubinstein-Taybi syndrome type 2 presenting as combined immunodeficiency
2018-01-01 Saettini, Francesco; Moratto, Daniele; Grioni, Andrea; Maitz, Silvia; Iascone, MARIA ROSARIA; Rizzari, Carmelo; Pavan, Fabio; Spinelli, Marco; Bettini, Laura Rachele; Biondi, Andrea; Badolato, Raffaele
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
Abnormal B-Cell Maturation and Increased Transitional B Cells in CBL Syndrome
2022-01-01 Saettini, F.; Coliva, T. A.; Vendemini, F.; Galbiati, M.; Bugarin, C.; Masetti, R.; Moratto, D.; Chiarini, M.; Guerra, F.; Iascone, M.; Badolato, R.; Cazzaniga, G.; Niemeyer, C.; Flotho, C.; Biondi, A.
Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency
2021-01-01 Saettini, F.; Poli, C.; Vengoechea, J.; Bonanomi, S.; Orellana, J. C.; Fazio, G.; Rodriguez III, F. H.; Noguera, L. P.; Booth, C.; Jarur-Chamy, V.; Shams, M.; Iascone, M.; Vukic, M.; Gasperini, S.; Quadri, M.; Seijas, A. B.; Rivers, E.; Mauri, M.; Badolato, R.; Cazzaniga, G.; Bugarin, C.; Gaipa, G.; Kroes, W. G. M.; Moratto, D.; van Oostaijen-Ten Dam, M. M.; Baas, F.; van der Maarel, S.; Piazza, R.; Coban-Akdemir, Z. H.; Lupski, J. R.; Yuan, B.; Chinn, I. K.; Daxinger, L.; Biondi, A.
Aicardi Goutieres Syndrome: New Insights on a Novel Set of Inborn Errors of Immunity
2014-01-01 Vairo, Donatella; Ferraro, R. M.; Moratto, Daniele; Pizzi, S.; Cattalini, Marco; Orcesi, S.; Tincani, Angela; Facchetti, Fabio; Galli, Jessica; Plebani, Alessandro; Crow, Y.; Notarangelo, L. D.; Plevani, P.; Fazzi, Elisa Maria; Giliani, Silvia Clara
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
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype
2015-01-01 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
Application of common recommendations for diagnosis and treatment of Wiskott-Aldrich syndrome and X-recessive piastrinopenia: clinical and immunological characteristics of 65 patients with WAS/XLT
2008-01-01 Soresina, Sa; Mazzolari, E; Notarangelo, Ld; Ventura, A; Locatelli, F; Dufour, C; Galanello, R; Zanesco, L; Izzi, G; De Mattia, D; Azzari, C; Cornelli, Pe; Rossi, P; Mazza, Cinzia; Moratto, Daniele; Giliani, Silvia Clara; Rondelli, R; Pession, A; Ugazio, Ag; Plebani, Alessandro
Atypical presentation of autoimmune lymphoproliferative syndrome due to CASP10 mutation
2016-01-01 Tripodi, Serena Ilaria; Mazza, Cinzia; Moratto, Daniele; Ramenghi, Ugo; Caorsi, Roberta; Gattorno, Marco; Badolato, Raffaele
Autologous Stem Cell Transplantation before Lymphocyte Apheresis for CAR-T Cells Therapy Negatively Impacts on T-Cells Fitness and NK Cell Levels in DLBCL Patients
2023-01-01 Farina, Mirko; Chiarini, Marco; Galvagni, Anna; Accorsi Buttini, Eugenia; Radici, Vera; Ferrari, Emilio; Bianchetti, Andrea; Beghin, Alessandra; Zuccalà, Francesco; Piva, Simone; Poli, Loris; Pilotto, Andrea; Leoni, Alessandro; Campisi, Giovanni; Re, Federica; Bernardi, Simona; Polverelli, Nicola; Morello, Enrico; Cattaneo, Chiara; Moratto, Daniele; Padovani, Alessandro; Lanfranchi, Arnalda; Almici, Camillo; Brugnoni, Duilio; Tucci, Alessandra; Malagola, Michele; Re, Alessandro; Russo, Domenico
Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia
2015-01-01 Crestani, Elena; Volpi, Stefano; Candotti, Fabio; Giliani, Silvia Clara; Notarangelo, Lucia Dora; Chu, Julia; Aldave Becerra, Juan Carlos; Buchbinder, David; Chou, Janet; Geha, Raif S.; Kanariou, Maria; King, Alejandra; Mazza, Cinzia; Moratto, Daniele; Sokolic, Robert; Garabedian, Elizabeth; Porta, Fulvio; Putti, Maria Caterina; Wakim, Rima H.; Tsitsikov, Erdyni; Pai, Sung Yun; Notarangelo, Luigi D.
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis
2023-01-01 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
Case Report: A Case of X-Linked Agammaglobulinemia With High Serum IgE Levels and Allergic Rhinitis
2020-01-01 Cinicola, B.; Uva, A.; Leonardi, L.; Moratto, D.; Giliani, S.; Carsetti, R.; Ferrari, S.; Zicari, A. M.; Duse, M.
Case Report: Analysis of Inflammatory Cytokines IL-6, CCL2/MCP1, CCL5/RANTES, CXCL9/MIG, and CXCL10/IP10 in a Cystic Fibrosis Patient Cohort During the First Wave of the COVID-19 Pandemic
2021-01-01 Baresi, G.; Giacomelli, M.; Moratto, D.; Chiarini, M.; Conforti, I. C.; Padoan, R.; Poli, P.; Timpano, S.; Caldarale, F.; Badolato, R.
Case Report: Hypomorphic Function and Somatic Reversion in DOCK8 Deficiency in One Patient With Two Novel Variants and Sclerosing Cholangitis
2021-01-01 Saettini, Francesco; Fazio, Grazia; Moratto, Daniele; Galbiati, Marta; Zucchini, Nicola; Ippolito, Davide; Dinelli, Marco Emilio; Imberti, Luisa; Mauri, Mario; Melzi, Maria Luisa; Bonanomi, Sonia; Gerussi, Alessio; Pinelli, Marinella; Barisani, Chiara; Bugarin, Cristina; Chiarini, Marco; Giacomelli, Mauro; Piazza, Rocco; Cazzaniga, Giovanni; Invernizzi, Pietro; Giliani, Silvia Clara; Badolato, Raffaele; Biondi, Andrea
CASE REPORT: IDENTIFICATION OF A PATIENT WITH FAMILIAR MUTATIONS AFFECTING BOTH WASP AND FOXP3 GENES
2012-01-01 Mazza, Cinzia; Moratto, Daniele; Masneri, Stefania; Vairo, Donatella; Plebani, Alessandro; Rovelli, A; Balduzzi, A; Corti, P; Giliani, Silvia Clara
Clinical and transcriptomic characteristics of a novel SMARCD2 mutation that disrupts neutrophil maturation and function
2023-01-01 Dotta, L.; Baresi, G.; Tamassia, N.; Calzetti, F.; Bianchetto-Aguilera, F.; Gasperini, S.; Gardiman, E.; Chiarini, M.; Moratto, D.; Martellosio, G.; Serana, F.; Micheletti, M.; Tregambe, D.; Pintabona, V.; Soncini, E.; Meini, A.; Girelli, M. F.; Beghin, A.; Lanfranchi, A.; Bugatti, M.; Brugnoni, D.; Soresina, A.; Plebani, A.; Cassatella, M.; Vermi, W.; Porta, F.; Badolato, R.
| 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 distinct human cell type expressing MHCII and RORγt with dual characteristics of dendritic cells and type 3 innate lymphoid cells | 1-gen-2023 | Ulezko Antonova, Alina; Lonardi, Silvia; Monti, Matilde; Missale, Francesco; Fan, Changxu; Coates, Matthew L; Bugatti, Mattia; Jaeger, Natalia; Fernandes Rodrigues, Patrick; Brioschi, Simone; Trsan, Tihana; Fachi, José L; Nguyen, Khai M; Nunley, Ryan M; Moratto, Daniele; Zini, Stefania; Kong, Lingjia; Deguine, Jacques; Peeples, Mark E; Xavier, Ramnik J; Clatworthy, Menna R; Wang, Ting; Cella, Marina; Vermi, William; Colonna, Marco | |
| 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 novel EP300 mutation associated with Rubinstein-Taybi syndrome type 2 presenting as combined immunodeficiency | 1-gen-2018 | Saettini, Francesco; Moratto, Daniele; Grioni, Andrea; Maitz, Silvia; Iascone, MARIA ROSARIA; Rizzari, Carmelo; Pavan, Fabio; Spinelli, Marco; Bettini, Laura Rachele; Biondi, Andrea; Badolato, Raffaele | |
| 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 | |
| Abnormal B-Cell Maturation and Increased Transitional B Cells in CBL Syndrome | 1-gen-2022 | Saettini, F.; Coliva, T. A.; Vendemini, F.; Galbiati, M.; Bugarin, C.; Masetti, R.; Moratto, D.; Chiarini, M.; Guerra, F.; Iascone, M.; Badolato, R.; Cazzaniga, G.; Niemeyer, C.; Flotho, C.; Biondi, A. | |
| Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency | 1-gen-2021 | Saettini, F.; Poli, C.; Vengoechea, J.; Bonanomi, S.; Orellana, J. C.; Fazio, G.; Rodriguez III, F. H.; Noguera, L. P.; Booth, C.; Jarur-Chamy, V.; Shams, M.; Iascone, M.; Vukic, M.; Gasperini, S.; Quadri, M.; Seijas, A. B.; Rivers, E.; Mauri, M.; Badolato, R.; Cazzaniga, G.; Bugarin, C.; Gaipa, G.; Kroes, W. G. M.; Moratto, D.; van Oostaijen-Ten Dam, M. M.; Baas, F.; van der Maarel, S.; Piazza, R.; Coban-Akdemir, Z. H.; Lupski, J. R.; Yuan, B.; Chinn, I. K.; Daxinger, L.; Biondi, A. | |
| Aicardi Goutieres Syndrome: New Insights on a Novel Set of Inborn Errors of Immunity | 1-gen-2014 | Vairo, Donatella; Ferraro, R. M.; Moratto, Daniele; Pizzi, S.; Cattalini, Marco; Orcesi, S.; Tincani, Angela; Facchetti, Fabio; Galli, Jessica; Plebani, Alessandro; Crow, Y.; Notarangelo, L. D.; Plevani, P.; Fazzi, Elisa Maria; Giliani, Silvia Clara | |
| 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 | |
| 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 | |
| Application of common recommendations for diagnosis and treatment of Wiskott-Aldrich syndrome and X-recessive piastrinopenia: clinical and immunological characteristics of 65 patients with WAS/XLT | 1-gen-2008 | Soresina, Sa; Mazzolari, E; Notarangelo, Ld; Ventura, A; Locatelli, F; Dufour, C; Galanello, R; Zanesco, L; Izzi, G; De Mattia, D; Azzari, C; Cornelli, Pe; Rossi, P; Mazza, Cinzia; Moratto, Daniele; Giliani, Silvia Clara; Rondelli, R; Pession, A; Ugazio, Ag; Plebani, Alessandro | |
| Atypical presentation of autoimmune lymphoproliferative syndrome due to CASP10 mutation | 1-gen-2016 | Tripodi, Serena Ilaria; Mazza, Cinzia; Moratto, Daniele; Ramenghi, Ugo; Caorsi, Roberta; Gattorno, Marco; Badolato, Raffaele | |
| Autologous Stem Cell Transplantation before Lymphocyte Apheresis for CAR-T Cells Therapy Negatively Impacts on T-Cells Fitness and NK Cell Levels in DLBCL Patients | 1-gen-2023 | Farina, Mirko; Chiarini, Marco; Galvagni, Anna; Accorsi Buttini, Eugenia; Radici, Vera; Ferrari, Emilio; Bianchetti, Andrea; Beghin, Alessandra; Zuccalà, Francesco; Piva, Simone; Poli, Loris; Pilotto, Andrea; Leoni, Alessandro; Campisi, Giovanni; Re, Federica; Bernardi, Simona; Polverelli, Nicola; Morello, Enrico; Cattaneo, Chiara; Moratto, Daniele; Padovani, Alessandro; Lanfranchi, Arnalda; Almici, Camillo; Brugnoni, Duilio; Tucci, Alessandra; Malagola, Michele; Re, Alessandro; Russo, Domenico | |
| Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia | 1-gen-2015 | Crestani, Elena; Volpi, Stefano; Candotti, Fabio; Giliani, Silvia Clara; Notarangelo, Lucia Dora; Chu, Julia; Aldave Becerra, Juan Carlos; Buchbinder, David; Chou, Janet; Geha, Raif S.; Kanariou, Maria; King, Alejandra; Mazza, Cinzia; Moratto, Daniele; Sokolic, Robert; Garabedian, Elizabeth; Porta, Fulvio; Putti, Maria Caterina; Wakim, Rima H.; Tsitsikov, Erdyni; Pai, Sung Yun; Notarangelo, Luigi D. | |
| 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 | |
| Case Report: A Case of X-Linked Agammaglobulinemia With High Serum IgE Levels and Allergic Rhinitis | 1-gen-2020 | Cinicola, B.; Uva, A.; Leonardi, L.; Moratto, D.; Giliani, S.; Carsetti, R.; Ferrari, S.; Zicari, A. M.; Duse, M. | |
| Case Report: Analysis of Inflammatory Cytokines IL-6, CCL2/MCP1, CCL5/RANTES, CXCL9/MIG, and CXCL10/IP10 in a Cystic Fibrosis Patient Cohort During the First Wave of the COVID-19 Pandemic | 1-gen-2021 | Baresi, G.; Giacomelli, M.; Moratto, D.; Chiarini, M.; Conforti, I. C.; Padoan, R.; Poli, P.; Timpano, S.; Caldarale, F.; Badolato, R. | |
| Case Report: Hypomorphic Function and Somatic Reversion in DOCK8 Deficiency in One Patient With Two Novel Variants and Sclerosing Cholangitis | 1-gen-2021 | Saettini, Francesco; Fazio, Grazia; Moratto, Daniele; Galbiati, Marta; Zucchini, Nicola; Ippolito, Davide; Dinelli, Marco Emilio; Imberti, Luisa; Mauri, Mario; Melzi, Maria Luisa; Bonanomi, Sonia; Gerussi, Alessio; Pinelli, Marinella; Barisani, Chiara; Bugarin, Cristina; Chiarini, Marco; Giacomelli, Mauro; Piazza, Rocco; Cazzaniga, Giovanni; Invernizzi, Pietro; Giliani, Silvia Clara; Badolato, Raffaele; Biondi, Andrea | |
| CASE REPORT: IDENTIFICATION OF A PATIENT WITH FAMILIAR MUTATIONS AFFECTING BOTH WASP AND FOXP3 GENES | 1-gen-2012 | Mazza, Cinzia; Moratto, Daniele; Masneri, Stefania; Vairo, Donatella; Plebani, Alessandro; Rovelli, A; Balduzzi, A; Corti, P; Giliani, Silvia Clara | |
| Clinical and transcriptomic characteristics of a novel SMARCD2 mutation that disrupts neutrophil maturation and function | 1-gen-2023 | Dotta, L.; Baresi, G.; Tamassia, N.; Calzetti, F.; Bianchetto-Aguilera, F.; Gasperini, S.; Gardiman, E.; Chiarini, M.; Moratto, D.; Martellosio, G.; Serana, F.; Micheletti, M.; Tregambe, D.; Pintabona, V.; Soncini, E.; Meini, A.; Girelli, M. F.; Beghin, A.; Lanfranchi, A.; Bugatti, M.; Brugnoni, D.; Soresina, A.; Plebani, A.; Cassatella, M.; Vermi, W.; Porta, F.; Badolato, R. |