Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Cirillo, Emilia"'
Autor:
Martire, Baldassarre, Azzari, Chiara, Badolato, Raffaele, Canessa, Clementina, Cirillo, Emilia, Gallo, Vera, Graziani, Simona, Lorenzini, Tiziana, Milito, Cinzia, Panza, Raffaella, Moschese, Viviana, Pignata, Claudio, Martire, B, Lassandro, G, Panza, R, Vacca, A, Marasco, C, Cardinale, F, Sisto, C, Pession, A, Ricci, G, Rondelli, R, Specchia, F, Plebani, A, Badolato, R, Lougaris, V, Soresina, A, Miniero, R, Anastasio, E, Paganelli, R, Dilizia, Sperli, D, Carpino, L, Cirillo, E, Gallo, V, Giardino, G, Spadaro, G, Pecoraro, A ), Putti, Mc, Agostini, C, Cinetto, F, Trizzino, A, Bertolini, P), Arlotta, A, Marseglia, Gl, Bossi, G, Consolini, R, Et, Al.
Publikováno v:
Vaccine. 36:7753
Autor:
Claudio Pignata, Maria Vittoria Barone, Emilia Cirillo, Giulia Scalia, Rosaria Prencipe, Mauro Magnani, Michele Menotta, Loredana Palamaro, Luigi Del Vecchio, Vera Gallo, Giuliana Giardino
Publikováno v:
Immunological investigations. 50(2-3)
Ataxia-Telangiectasia (A-T) is characterized by cerebellar neurodegeneration and immunodeficiency. Recent studies suggest that very low glucocorticoids (GCs) doses may help improve A-T neurological phenotype in some patients. Interestingly, in GCs st
Autor:
Claudio Pignata, Giuliana Giardino, Carol J Saunders, Antonio Leonardi, Rosaria Prencipe, Anne Durandy, Emilia Cirillo, Vincenzo Martinelli, Viviana Moschese, Alessio Lepore, Gigliola Di Matteo, Luigi Del Vecchio, Giulia Scalia, Vera Gallo
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 3, p 818 (2020)
Journal of Clinical Medicine
Volume 9
Issue 3
Journal of Clinical Medicine
Volume 9
Issue 3
Very high IgM levels represent the hallmark of hyper IgM (HIGM) syndromes, a group of primary immunodeficiencies (PIDs) characterized by susceptibility to infections and malignancies. Other PIDs not fulfilling the diagnostic criteria for HIGM syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de0092bbf788e84648eeff417f3ec37b
http://hdl.handle.net/2108/241084
http://hdl.handle.net/2108/241084
Autor:
Baldassarre Martire, Luciana Chessa, Alessandro Plebani, Francesca Conti, Andrea Finocchi, Francesca Ferrua, Laura Dotta, Clementina Canessa, Vassilios Lougaris, Donato Amodio, Emilia Cirillo, Davide Montin, Federica Barzaghi, Franco Locatelli, Alberto Tommasini, Viviana Moschese, Maria Pia Cicalese, Rosa Maria Dellepiane, Andrea Pession, Chiara Azzari, Lucia Augusta Baselli, Caterina Cancrini, Maria Caterina Putti, Raffaele Badolato, Alessandro Aiuti, Claudio Pignata, Annarosa Soresina, Roberta Romano, Silvia Ricci, Agata Polizzi, Antonio Marzollo, Giuliana Giardino
Medical advances have dramatically improved the long-term prognosis of children and adolescents with inborn errors of immunity (IEIs). Transfer of the medical care of individuals with pediatric IEIs to adult facilities is also a complex task because
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db8ead20b8d96f7d30d7b6edbf1edef8
https://hdl.handle.net/10807/229753
https://hdl.handle.net/10807/229753
Autor:
Maria Caterina Putti, Fernando Specchia, Andrea Pession, Alberto Tommasini, Paolo Rossi, Alessandro Aiuti, Andrea Finocchi, Emilia Cirillo, Federica Barzaghi, Caterina Cancrini, Alessandro Plebani, Davide Montin, Irene D'Alba, Baldassarre Martire, Silvana Martino, Raffaele Badolato, Rita Consolini, Gigliola Di Matteo, Franco Locatelli, Paolo Pierani, Federica Esposito, Chiara Azzari, Enrico Attardi, Claudio Pignata, Antonio Marzollo, Silvia Giliani, Samuele Naviglio, Maria Pia Cicalese, Giuliana Giardino, Giuseppe Quaremba, Vassilios Lougaris, Rosaria Prencipe, Alessia Scarselli, Silvia Ricci, Fiorentino Grasso
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Frontiers in Immunology
Frontiers in Immunology
Severe combined immunodeficiencies (SCIDs) are a group of inborn errors of the immune system, usually associated with severe or life-threatening infections. Due to the variability of clinical phenotypes, the diagnostic complexity and the heterogeneit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bfc66a3d3260ea7d2625404b6240f20
http://hdl.handle.net/2158/1174238
http://hdl.handle.net/2158/1174238
Autor:
Giuseppe Quaremba, Vincenzo Graziano, Fiorentino Grasso, Vera Gallo, Sergio Motta, Emilia Cirillo, Claudio Pignata, Carmine Botta, Letizia Cruoglio
Otorhinolaryngologic manifestations are common in 22q11.2 deletion syndrome (22q11.2DS), but poorly described. This study aimed to better define the ear-nose-throat (ENT) phenotype of 22q11.2DS patients, in the attempt to best detect subjects requiri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0b5c3f52be80ba11f4e8befe8e5dd8b
http://hdl.handle.net/11588/719896
http://hdl.handle.net/11588/719896
Autor:
Giuliana Giardino, Maia De Luca, Emilia Cirillo, Paolo Palma, Roberta Romano, Massimiliano Valeriani, Laura Papetti, Carol Saunders, Caterina Cancrini, Claudio Pignata
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Vol 8 (2017)
Frontiers in Immunology, Vol 8 (2017)
Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal hyperinflammatory condition. Variants in different genes have been associated with the familial forms of the syndrome (FHL), usually presenting within the first 2 years of life. Due to i
Autor:
Vera Gallo, Rosaria Prencipe, Donatella Capalbo, Giovanni Gaudino, Chiara Di Giacomo, Roberta Romano, Giuliana Giardino, Claudio Pignata, Marco De Cataldis, Paola Lorello, Loredana Palamaro, Emilia Cirillo, Roberta D'Assante
Publikováno v:
Frontiers in Pediatrics
Frontiers in Pediatrics, Vol 4 (2016)
Frontiers in Pediatrics, Vol 4 (2016)
Increased risk of developing autoimmune manifestations has been identified in different primary immunodeficiencies (PID). In such conditions, autoimmunity and immune deficiency represent intertwined phenomena that reflect inadequate immune function.
Autor:
Tiziana Esposito, Claudio Pignata, Vera Gallo, Emilia Cirillo, Giuliana Giardino, Roberta Naddei, Filomena Maio, Fiorentino Grasso
Publikováno v:
Scandinavian Journal of Gastroenterology. 49:274-279
Objective. Enteropathy is a very common feature in patients with primary immunodeficiencies. In patients with Del22 gastrointestinal (GI) alterations, including feeding disorders and congenital abnormalities have been often reported, mostly in the fi
Autor:
Valentina Rubino, Matilde Valeria Ursini, Giuliana Giardino, Raffaele Badolato, Giuseppina Ruggiero, Anne Puel, Donatella Vairo, Emilia Cirillo, Domenico Somma, Rita Carsetti, Claudio Pignata, Antonio Leonardi, Giuseppe Terrazzano
Publikováno v:
Pediatric allergy and immunology 27 (2016): 220–223. doi:10.1111/pai.12496
info:cnr-pdr/source/autori:Giardino, Giuliana; Somma, Domenico; Cirillo, Emilia; Ruggiero, Giuseppina; Terrazzano, Giuseppe; Rubino, Valentina; Ursini, Matilde Valeria; Vairo, Donatella; Badolato, Raffaele; Carsetti, Rita; Leonardi, Antonio; Puel, Anne; Pignata, Claudio/titolo:Novel STAT1 gain-of-function mutation and suppurative infections/doi:10.1111%2Fpai.12496/rivista:Pediatric allergy and immunology/anno:2016/pagina_da:220/pagina_a:223/intervallo_pagine:220–223/volume:27
info:cnr-pdr/source/autori:Giardino, Giuliana; Somma, Domenico; Cirillo, Emilia; Ruggiero, Giuseppina; Terrazzano, Giuseppe; Rubino, Valentina; Ursini, Matilde Valeria; Vairo, Donatella; Badolato, Raffaele; Carsetti, Rita; Leonardi, Antonio; Puel, Anne; Pignata, Claudio/titolo:Novel STAT1 gain-of-function mutation and suppurative infections/doi:10.1111%2Fpai.12496/rivista:Pediatric allergy and immunology/anno:2016/pagina_da:220/pagina_a:223/intervallo_pagine:220–223/volume:27
Chronic mucocutaneous candidiasis (CMCC) is a heterogeneous group of disorders characterized by non-invasive persistent Candida species infections of the skin, nails, and mucous membranes. Heterozygous dominant gain-of-function (GOF) mutations in sig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d25495fe4465ae307f0bf250b7841ee
http://hdl.handle.net/11588/614597
http://hdl.handle.net/11588/614597