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 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
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
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: 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
Collapse of the Plasmacytoid Dendritic Cells compartment in advanced cutaneous melanomas by components of the tumor cell secretome
2019-01-01 Vescovi, Raffaella; Monti, Matilde; Moratto, Daniele; Paolini, Lucia; Consoli, Francesca; Benerini Gatta, Luisa; Melocchi, Laura; Calza, Stefano; Chiudinelli, Mariella; Rossi, Giulio; Bugatti, Mattia; Maio, Michele; Fonsatti, Ester; Farisoglio, Camillo; Simbolo, Michele; Almici, Camillo; Verardi, Rosanna; Scarpa, Aldo; Bergese, Paolo; Manganoni, Ausilia; Facchetti, Fabio; Vermi, William
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in 3 brothers with diarrhea, eczema, and infections
2013-01-01 Dinwiddie, D. L.; Kingsmore, S. F.; Caracciolo, S.; Rossi, G.; Moratto, D.; Mazza, C.; Sabelli, C.; Bacchetta, R.; Passerini, L.; Magri, C.; Bell, C. J.; Miller, N. A.; Hateley, S. L.; Saunders, C. J.; Zhang, L.; Schroth, G. P.; Barlati, S.; Badolato, R.
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in three brothers with diarrhea, eczema and infections.
2013-01-01 Darrell L., Dinwiddie; Stephen F., Kingsmore; Sonia, Caracciolo; Giuseppe, Rossi; Moratto, Daniele; Cinzia, Mazza; Cristiano, Sabelli; Rosa, Bacchetta; Laura, Passerini; Magri, Chiara; Callum J., Bell; Neil A., Miller; Shannon L., Hateley; Carol J., Saunders; Lu, Zhang; Gary P., Schroth; Barlati, Sergio; Badolato, Raffaele
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
Defective migration of monocyte-derived dendritic cells in LAD-1 immunodeficiency.
2002-01-01 Fiorini, Maurilia; Vermi, William; Facchetti, Fabio; Moratto, Daniele; Alessandri, Giulio; Notarangelo, L.; Caruso, Arnaldo; Grigolato, Pier Giovanni; Ugazio, Alberto Giovanni; Notarangelo, Luigi Daniele; Badolato, Raffaele
| 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 | |
| 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 | |
| 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 | |
| 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: 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 | |
| Collapse of the Plasmacytoid Dendritic Cells compartment in advanced cutaneous melanomas by components of the tumor cell secretome | 1-gen-2019 | Vescovi, Raffaella; Monti, Matilde; Moratto, Daniele; Paolini, Lucia; Consoli, Francesca; Benerini Gatta, Luisa; Melocchi, Laura; Calza, Stefano; Chiudinelli, Mariella; Rossi, Giulio; Bugatti, Mattia; Maio, Michele; Fonsatti, Ester; Farisoglio, Camillo; Simbolo, Michele; Almici, Camillo; Verardi, Rosanna; Scarpa, Aldo; Bergese, Paolo; Manganoni, Ausilia; Facchetti, Fabio; Vermi, William | |
| Combined DOCK8 and CLEC7A mutations causing immunodeficiency in 3 brothers with diarrhea, eczema, and infections | 1-gen-2013 | Dinwiddie, D. L.; Kingsmore, S. F.; Caracciolo, S.; Rossi, G.; Moratto, D.; Mazza, C.; Sabelli, C.; Bacchetta, R.; Passerini, L.; Magri, C.; Bell, C. J.; Miller, N. A.; Hateley, S. L.; Saunders, C. J.; Zhang, L.; Schroth, G. P.; Barlati, S.; Badolato, R. | |
| Combined DOCK8 and CLEC7A mutations causing immunodeficiency in three brothers with diarrhea, eczema and infections. | 1-gen-2013 | Darrell L., Dinwiddie; Stephen F., Kingsmore; Sonia, Caracciolo; Giuseppe, Rossi; Moratto, Daniele; Cinzia, Mazza; Cristiano, Sabelli; Rosa, Bacchetta; Laura, Passerini; Magri, Chiara; Callum J., Bell; Neil A., Miller; Shannon L., Hateley; Carol J., Saunders; Lu, Zhang; Gary P., Schroth; Barlati, Sergio; Badolato, Raffaele | |
| 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 | |
| Defective migration of monocyte-derived dendritic cells in LAD-1 immunodeficiency. | 1-gen-2002 | Fiorini, Maurilia; Vermi, William; Facchetti, Fabio; Moratto, Daniele; Alessandri, Giulio; Notarangelo, L.; Caruso, Arnaldo; Grigolato, Pier Giovanni; Ugazio, Alberto Giovanni; Notarangelo, Luigi Daniele; Badolato, Raffaele |