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Eleonora Gambineri

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Chemicals & Drugs

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Kevin Goudy; Silvana Martino; Sven Olek; Maurilio Ponzoni; Maria Grazia Roncarolo; Alberto Tommasini; Marina Vignoli; Sara Ciullini Mannurita; Alessandro Aiuti; Andrea Assanelli; Didem Aydin; Federica Barzaghi; Immacolata Brigida; Maria Pia Cicalese; Fabio Ciceri; Rosa Maria Dellepiane; Claudio Doglioni; Eleonora Gambineri; Rosa Bacchetta
Human IL2RA null mutation mediates immunodeficiency with lymphoproliferation and autoimmunity.
F Barzaghi; Caterina Cancrini; M Cecconi; Y H Choe; R Ciccocioppo; S Ciullini Mannurita; T Cornu; S Corrente; V Discepolo; Eleonora Gambineri; A Ikinciogullari; E S Kang; S Olek; Laura Passerini; Maria-Grazia Roncarolo; Claudia Sartirana; J Schmidtko; G Zuin; alessandro ambrosi; Rosa Bacchetta
Demethylation analysis of the FOXP3 locus shows quantitative defects of regulatory T cells in IPEX-like syndrome.
Francesca Fioredda; Eleonora Gambineri; Roberta Ghilardi; Marina Lanciotti; Baldassarre Martire; Giuseppe Menna; Giovanni Palazzi; Marta Pillon; Anna Pusiol; Ugo Ramenghi; Daniela Renga; Fabio Tucci; Angelica Barone; Sonia Bonanomi; Michaela Calvillo; Gabriella Casazza; Tiziana Coliva; Piero Farruggia; Carlo Dufour
Congenital and acquired neutropenias consensus guidelines on therapy and follow-up in childhood from the Neutropenia Committee of the Marrow Failure Syndrome Group of the AIEOP (Associazione Italiana Emato-Oncologia Pediatrica).

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All Publications

2013: Kevin Goudy; Silvana Martino; Sven Olek; Maurilio Ponzoni; Maria Grazia Roncarolo; Alberto Tommasini; Marina Vignoli; Sara Ciullini Mannurita; Alessandro Aiuti; Andrea Assanelli; Didem Aydin; Federica Barzaghi; Immacolata Brigida; Maria Pia Cicalese; Fabio Ciceri; Rosa Maria Dellepiane; Claudio Doglioni; Eleonora Gambineri; Rosa Bacchetta
Human IL2RA null mutation mediates immunodeficiency with lymphoproliferation and autoimmunity.
Clinical immunology (Orlando, Fla.) 2013;146(3):248-61.
2012: F Barzaghi; Caterina Cancrini; M Cecconi; Y H Choe; R Ciccocioppo; S Ciullini Mannurita; T Cornu; S Corrente; V Discepolo; Eleonora Gambineri; A Ikinciogullari; E S Kang; S Olek; Laura Passerini; Maria-Grazia Roncarolo; Claudia Sartirana; J Schmidtko; G Zuin; alessandro ambrosi; Rosa Bacchetta
Demethylation analysis of the FOXP3 locus shows quantitative defects of regulatory T cells in IPEX-like syndrome.
Journal of autoimmunity 2012;38(1):49-58.
2012: Francesca Fioredda; Eleonora Gambineri; Roberta Ghilardi; Marina Lanciotti; Baldassarre Martire; Giuseppe Menna; Giovanni Palazzi; Marta Pillon; Anna Pusiol; Ugo Ramenghi; Daniela Renga; Fabio Tucci; Angelica Barone; Sonia Bonanomi; Michaela Calvillo; Gabriella Casazza; Tiziana Coliva; Piero Farruggia; Carlo Dufour
Congenital and acquired neutropenias consensus guidelines on therapy and follow-up in childhood from the Neutropenia Committee of the Marrow Failure Syndrome Group of the AIEOP (Associazione Italiana Emato-Oncologia Pediatrica).
American journal of hematology 2012;87(2):238-43.
2012: D Zennaro; D Pomponi; G Russo; Enrico Scala; Diego Arcelli; Elisabetta Caprini; Eleonora Gambineri; A Mari
Proteomics plus genomics approaches in primary immunodeficiency: the case of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome.
Clinical and experimental immunology 2012;167(1):120-8.
2011: Laura Passerini; Sara Di Nunzio; Silvia Gregori; Eleonora Gambineri; Massimiliano Cecconi; Markus G Seidel; Giantonio Cazzola; Lucia Perroni; Alberto Tommasini; Silvia Vignola; Luisa Guidi; Maria-Grazia Roncarolo; Rosa Bacchetta
Functional type 1 regulatory T cells develop regardless of FOXP3 mutations in patients with IPEX syndrome.
European journal of immunology 2011;41(4):1120-31.
2010: Stefano Stagi; Elisabetta Lapi; Eleonora Gambineri; Cristina Manoni; Maurizio Genuardi; Gloria Colarusso; Camilla Conti; Francesco Chiarelli; Maurizio de Martino; Chiara Azzari
Bone density and metabolism in subjects with microdeletion of chromosome 22q11 (del22q11).
European journal of endocrinology / European Federation of Endocrine Societies 2010;163(2):329-37.
2010: Stefano Stagi; Elisabetta Lapi; Eleonora Gambineri; Roberto Salti; Maurizio Genuardi; Gloria Colarusso; Camilla Conti; Rita Jenuso; Francesco Chiarelli; Chiara Azzari; Maurizio de Martino
Thyroid function and morphology in subjects with microdeletion of chromosome 22q11 (del(22)(q11)).
Clinical endocrinology 2010;72(6):839-44.
2010: Gloria Colarusso; Eleonora Gambineri; Elisabetta Lapi; Tommaso Casini; Fabio Tucci; Francesca Lippi; Chiara Azzari
Evans syndrome and antibody deficiency: an atypical presentation of chromosome 22q11.2 deletion syndrome.
Pediatric reports 2010;2(2):e13.
2010: Biagio Olivito; Andrea Taddio; Gabriele Simonini; Cristina Massai; Sara Ciullini; Eleonora Gambineri; Maurizio de Martino; Chiara Azzari; Rolando Cimaz
Defective FOXP3 expression in patients with acute Kawasaki disease and restoration by intravenous immunoglobulin therapy.
Clinical and experimental rheumatology 2010;28(1 Suppl 57):93-7.
2009: Biagio Olivito; Gabriele Simonini; Sara Ciullini; Maria Moriondo; Letizia Betti; Eleonora Gambineri; Luca Cantarini; Maurizio de Martino; Chiara Azzari; Rolando Cimaz
Th17 transcription factor RORC2 is inversely correlated with FOXP3 expression in the joints of children with juvenile idiopathic arthritis.
The Journal of rheumatology 2009;36(9):2017-24.
2008: Chiara Azzari; Maria Moriondo; Giuseppe Indolfi; Letizia Betti; Eleonora Gambineri; Maurizio de Martino; Massimo Resti
Higher risk of hepatitis C virus perinatal transmission from drug user mothers is mediated by peripheral blood mononuclear cell infection.
Journal of medical virology 2008;80(1):65-71.
2007: Rosa Bacchetta; Eleonora Gambineri; Maria-Grazia Roncarolo
Role of regulatory T cells and FOXP3 in human diseases.
The Journal of allergy and clinical immunology 2007;120(2):227-35; quiz 236-7.
2007: Troy R Torgerson; Avriel Linane; Nicolette Moes; Stephanie Anover; Véronique Mateo; Frédéric Rieux-Laucat; Olivier Hermine; Shashi Vijay; Eleonora Gambineri; Nadine Cerf-Bensussan; Alain Fischer; Hans D Ochs; Olivier Goulet; Frank M Ruemmele
Severe food allergy as a variant of IPEX syndrome caused by a deletion in a noncoding region of the FOXP3 gene.
Gastroenterology 2007;132(5):1705-17.
2007: Hans D Ochs; Eleonora Gambineri; Troy R Torgerson
IPEX, FOXP3 and regulatory T-cells: a model for autoimmunity.
Immunologic research 2007;38(1-3):112-21.
2006: Rosa Bacchetta; Laura Passerini; Eleonora Gambineri; Minyue Dai; Sarah E Allan; Lucia Perroni; Franca Dagna Bricarelli; Claudia Sartirana; Susanne Matthes-Martin; Anita Lawitschka; Chiara Azzari; Steven F Ziegler; Megan K Levings; Maria-Grazia Roncarolo
Defective regulatory and effector T cell functions in patients with FOXP3 mutations.
The Journal of clinical investigation 2006;116(6):1713-22.
2005: Chiara Azzari; Eleonora Gambineri; Massimo Resti; Maria Moriondo; Letizia Betti; Lucien Rojas Saldias; Anna M G Gelli; Alberto Vierucci
Safety and immunogenicity of measles-mumps-rubella vaccine in children with congenital immunodeficiency (DiGeorge syndrome).
Vaccine 2005;23(14):1668-71.
2003: Wen-I Lee; Quli Zhu; Eleonora Gambineri; Yinzhu Jin; Andrew A Welcher; Hans D Ochs
Inducible CO-stimulator molecule, a candidate gene for defective isotype switching, is normal in patients with hyper-IgM syndrome of unknown molecular diagnosis.
The Journal of allergy and clinical immunology 2003;112(5):958-64.
2003: Eleonora Gambineri; Troy R Torgerson; Hans D Ochs
Immune dysregulation, polyendocrinopathy, enteropathy, and X-linked inheritance (IPEX), a syndrome of systemic autoimmunity caused by mutations of FOXP3, a critical regulator of T-cell homeostasis.
Current opinion in rheumatology 2003;15(4):430-5.
2001: Chiara Azzari; Massimo Resti; Maria Moriondo; Eleonora Gambineri; ME Rossi; Elio Novembre; Alberto Vierucci
Lack of transmission of TT virus through immunoglobulins.
Transfusion 2001;41(12):1505-8.