GAMBINERI, ELEONORA
GAMBINERI, ELEONORA
Neuroscienze, Psicologia, Area del Farmaco e Salute del Bambino (NEUROFARBA)
A case of antibody deficiency: CVID or XLA?
2005 E. GAMBINERI
A case of isolated CD4+ T cell deficiency and recurrent parotitis.
2008 CATANIA P; BERTI L; GELLI AMG; BACCINI A; RESTI M; DE MARTINO M; AZZARI C; GAMBINERI E.
A case of recurrent lower respiratory infections
2008 Colarusso, G.; Lippi, F.; Gambineri E, Lombardi, E.; Bianchi, L.; Gelli, A. M. G.; Azzari, C.
A Nationwide Study of GATA2 Deficiency in Italy Reveals Novel Symptoms and Genotype–phenotype Association
2023 Roncareggi, Samuele; Girardi, Katia; Fioredda, Francesca; Pedace, Lucia; Arcuri, Luca; Badolato, Raffaele; Bonanomi, Sonia; Borlenghi, Erika; Cirillo, Emilia; Coliva, Tiziana; Consonni, Filippo; Conti, Francesca; Farruggia, Piero; Gambineri, Eleonora; Guerra, Fabiola; Locatelli, Franco; Mancuso, Gaia; Marzollo, Antonio; Masetti, Riccardo; Micalizzi, Concetta; Onofrillo, Daniela; Piccini, Matteo; Pignata, Claudio; Raddi, Marco Gabriele; Santini, Valeria; Vendemini, Francesca; Biondi, Andrea; Saettini, Francesco
A NEW CASE OF IPEX RECEIVING BONE MARROW TRANSPLANTATION.
2005 E. MAZZOLARI;C. FIORINO; M. FONTANA;C. D'IPPOLITO; A. LANFRANCHI; E. GAMBINERI; H. OCHS; R. BADOLATO; L.D. NOTARANGELO
A patient affected by SCN with long term CSF3R acquired mutation and no progression in MDS/AML
2008 Giunti, L.; Gambineri E; Casini, T.; Arico, M.; Tucci, F.
A silent FOXP3 mutation (c.543C > T, S181S) possibly responsible of atypical IPEX phenotype
2008 Gambineri E, Bianchi, L.; Giunti, L.; Mannurita, Ciullini S.; Azzari, C.
Allogeneic Hematopoietic Stem Cell Transplantation for Congenital Immune Dysregulatory Disorders
2019 Shahrzad Bakhtiar, Julia Fekadu, Markus G SeideL, Eleonora Gambineri
ALPS, FAS, and beyond: from inborn errors of immunity to acquired immunodeficiencies
2022 Consonni F.; Gambineri E.; Favre C.
AN ATYPICAL CASE OF IPEX SINDROME WITH MULTIPLE FOXP3 MUTATIONS
2004 E. GAMBINERI; L. BIANCHI; A. ET
Anti-infective prophylaxis for primary immunodeficiencies: what is done in Italian Primary Immunodeficiency Network centers (IPINet) and review of the literature.
2013 Moschese V;Martire B;Soresina A;Chini L;Graziani S;Monteferrario E;Bacchetta R;Cancrini C;Fiorilli M;Gambineri E;Pession A;Pignata C;Quinti I;Rondelli R;Rossi P;Ugazio AG;Plebani A;Pietrogrande MC
Atypical Presentations of IPEX: Expect the Unexpected
2021 Consonni F.; Ciullini Mannurita S.; Gambineri E.
Autoimmune Cytopenias and Dysregulated Immunophenotype Act as Warning Signs of Inborn Errors of Immunity: Results From a Prospective Study
2022 Schiavo E.; Martini B.; Attardi E.; Consonni F.; Ciullini Mannurita S.; Coniglio M.L.; Tellini M.; Chiocca E.; Fotzi I.; Luti L.; D'Alba I.; Veltroni M.; Favre C.; Gambineri E.
Bone density and metabolism in subjects with microdeletion of chromosome 22q11 (del22q11)
2010 Stagi S.; Lapi E.; Gambineri E.; Manoni C.; Genuardi M.; Colarusso G.; Conti C.; Chiarelli F.; de Martino M.; Azzari C.
CACP syndrome: identification of five novel mutations and of the first case of UPD in the largest European cohort
2013 Sara Ciullini Mannurita;Marina Vignoli;Lucia Bianchi;Anuela Kondi;Valeria Gerloni;Luciana Breda;Rebecca ten Cate;Maria Alessio;Angelo Ravelli;Fernanda Falcini;Eleonora Gambineri
Case Report: A Novel Pathogenic Missense Mutation in FAS: A Multi-Generational Case Series of Autoimmune Lymphoproliferative Syndrome
2021 Gaefke C.L.; Metts J.; Imanirad D.; Nieves D.; Terranova P.; Dell'Orso G.; Gambineri E.; Miano M.; Lockey R.F.; Walter J.E.; Westermann-Clark E.
Case Report: Signal Transducer and Activator of Transcription 3 Gain-of-Function and Spectrin Deficiency: A Life-Threatening Case of Severe Hemolytic Anemia
2021 Ciullini Mannurita S.; Goda R.; Schiavo E.; Coniglio M.L.; Azzali A.; Fotzi I.; Tondo A.; Tintori V.; Frenos S.; Sanvito M.C.; Vignoli M.; Luceri C.; Bigagli E.; Grassi A.; D'Elios M.M.; Favre C.; Gambineri E.
CD25 deficiency: A new conformational mutation prevents the receptor expression on cell surface
2019 Vignoli M.; Ciullini Mannurita S.; Fioravanti A.; Tumino M.; Grassi A.; Guariso G.; Favre C.; D'Elios M.M.; Gambineri E.
CD4+CD25+Foxp3+T regulatory cells expression in peripheral blood can not be induced by oral desensitisation
2007 Francesca, M.; Li, G. Gel; Bianchi, L.; Gambineri E.; Pucci, N.; Bernardini, R.; Rossi, M.; Azzari, C.; Novembre, E.
Chronic granulomatous disease in two adolescent males: uncommon mild presentation
2005 Baccini A; Azzari C; Carbonella R; Gambineri E; Lippi F; Vierucci A; Indolfi G; de Martino M.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A case of antibody deficiency: CVID or XLA? | 2005 | E. GAMBINERI | |
| A case of isolated CD4+ T cell deficiency and recurrent parotitis. | 2008 | CATANIA P; BERTI L; GELLI AMG; BACCINI A; RESTI M; DE MARTINO M; AZZARI C; GAMBINERI E. | |
| A case of recurrent lower respiratory infections | 2008 | Colarusso, G.; Lippi, F.; Gambineri E, Lombardi, E.; Bianchi, L.; Gelli, A. M. G.; Azzari, C. | |
| A Nationwide Study of GATA2 Deficiency in Italy Reveals Novel Symptoms and Genotype–phenotype Association | 2023 | Roncareggi, Samuele; Girardi, Katia; Fioredda, Francesca; Pedace, Lucia; Arcuri, Luca; Badolato, Raffaele; Bonanomi, Sonia; Borlenghi, Erika; Cirillo, Emilia; Coliva, Tiziana; Consonni, Filippo; Conti, Francesca; Farruggia, Piero; Gambineri, Eleonora; Guerra, Fabiola; Locatelli, Franco; Mancuso, Gaia; Marzollo, Antonio; Masetti, Riccardo; Micalizzi, Concetta; Onofrillo, Daniela; Piccini, Matteo; Pignata, Claudio; Raddi, Marco Gabriele; Santini, Valeria; Vendemini, Francesca; Biondi, Andrea; Saettini, Francesco | |
| A NEW CASE OF IPEX RECEIVING BONE MARROW TRANSPLANTATION. | 2005 | E. MAZZOLARI;C. FIORINO; M. FONTANA;C. D'IPPOLITO; A. LANFRANCHI; E. GAMBINERI; H. OCHS; R. BADOLATO; L.D. NOTARANGELO | |
| A patient affected by SCN with long term CSF3R acquired mutation and no progression in MDS/AML | 2008 | Giunti, L.; Gambineri E; Casini, T.; Arico, M.; Tucci, F. | |
| A silent FOXP3 mutation (c.543C > T, S181S) possibly responsible of atypical IPEX phenotype | 2008 | Gambineri E, Bianchi, L.; Giunti, L.; Mannurita, Ciullini S.; Azzari, C. | |
| Allogeneic Hematopoietic Stem Cell Transplantation for Congenital Immune Dysregulatory Disorders | 2019 | Shahrzad Bakhtiar, Julia Fekadu, Markus G SeideL, Eleonora Gambineri | |
| ALPS, FAS, and beyond: from inborn errors of immunity to acquired immunodeficiencies | 2022 | Consonni F.; Gambineri E.; Favre C. | |
| AN ATYPICAL CASE OF IPEX SINDROME WITH MULTIPLE FOXP3 MUTATIONS | 2004 | E. GAMBINERI; L. BIANCHI; A. ET | |
| Anti-infective prophylaxis for primary immunodeficiencies: what is done in Italian Primary Immunodeficiency Network centers (IPINet) and review of the literature. | 2013 | Moschese V;Martire B;Soresina A;Chini L;Graziani S;Monteferrario E;Bacchetta R;Cancrini C;Fiorilli M;Gambineri E;Pession A;Pignata C;Quinti I;Rondelli R;Rossi P;Ugazio AG;Plebani A;Pietrogrande MC | |
| Atypical Presentations of IPEX: Expect the Unexpected | 2021 | Consonni F.; Ciullini Mannurita S.; Gambineri E. | |
| Autoimmune Cytopenias and Dysregulated Immunophenotype Act as Warning Signs of Inborn Errors of Immunity: Results From a Prospective Study | 2022 | Schiavo E.; Martini B.; Attardi E.; Consonni F.; Ciullini Mannurita S.; Coniglio M.L.; Tellini M.; Chiocca E.; Fotzi I.; Luti L.; D'Alba I.; Veltroni M.; Favre C.; Gambineri E. | |
| Bone density and metabolism in subjects with microdeletion of chromosome 22q11 (del22q11) | 2010 | Stagi S.; Lapi E.; Gambineri E.; Manoni C.; Genuardi M.; Colarusso G.; Conti C.; Chiarelli F.; de Martino M.; Azzari C. | |
| CACP syndrome: identification of five novel mutations and of the first case of UPD in the largest European cohort | 2013 | Sara Ciullini Mannurita;Marina Vignoli;Lucia Bianchi;Anuela Kondi;Valeria Gerloni;Luciana Breda;Rebecca ten Cate;Maria Alessio;Angelo Ravelli;Fernanda Falcini;Eleonora Gambineri | |
| Case Report: A Novel Pathogenic Missense Mutation in FAS: A Multi-Generational Case Series of Autoimmune Lymphoproliferative Syndrome | 2021 | Gaefke C.L.; Metts J.; Imanirad D.; Nieves D.; Terranova P.; Dell'Orso G.; Gambineri E.; Miano M.; Lockey R.F.; Walter J.E.; Westermann-Clark E. | |
| Case Report: Signal Transducer and Activator of Transcription 3 Gain-of-Function and Spectrin Deficiency: A Life-Threatening Case of Severe Hemolytic Anemia | 2021 | Ciullini Mannurita S.; Goda R.; Schiavo E.; Coniglio M.L.; Azzali A.; Fotzi I.; Tondo A.; Tintori V.; Frenos S.; Sanvito M.C.; Vignoli M.; Luceri C.; Bigagli E.; Grassi A.; D'Elios M.M.; Favre C.; Gambineri E. | |
| CD25 deficiency: A new conformational mutation prevents the receptor expression on cell surface | 2019 | Vignoli M.; Ciullini Mannurita S.; Fioravanti A.; Tumino M.; Grassi A.; Guariso G.; Favre C.; D'Elios M.M.; Gambineri E. | |
| CD4+CD25+Foxp3+T regulatory cells expression in peripheral blood can not be induced by oral desensitisation | 2007 | Francesca, M.; Li, G. Gel; Bianchi, L.; Gambineri E.; Pucci, N.; Bernardini, R.; Rossi, M.; Azzari, C.; Novembre, E. | |
| Chronic granulomatous disease in two adolescent males: uncommon mild presentation | 2005 | Baccini A; Azzari C; Carbonella R; Gambineri E; Lippi F; Vierucci A; Indolfi G; de Martino M. |