GALLO, VERA
GALLO, VERA
Intergenerational familial phenotipic variability in 22Q11.2 subjects: a multicenter study within the italian primary immunodeficiencies network (IPINET)
2012 Cirillo, Emilia; Giardino, Giuliana; Gallo, Vera; Puliafito, P.; Ariganello, P.; Azzari, C.; Cardinale, F.; Consolini, R.; Martino, S.; Plebani, A.; Scarano, G.; Soresina, A. R.; Cancrini, C.; Digilio, M. C.; Pignata, Claudio
Evaluation of executive functions in subjects affected with 22Q11.2 deletion syndrome: a neuroanatomical hypothesis
2012 Marino, M.; Riccio, M. P.; Tiano, C.; Cirillo, Emilia; Maio, F.; Gallo, Vera; Esposito, T.; Roberta, N.; Pignata, Claudio; Bravaccio, Carmela
Retrospective analysis of 21 pediatric patients affected with hemophagocytic syndrome of unknown genetic cause: clinical features and outcome
2012 Veropalumbo, C.; Giardino, Giuliana; Cirillo, Emilia; Gallo, Vera; Maio, F.; Esposito, T.; Naddei, R.; Grasso, F.; Poggi, V.; De Fusco, C.; Pignata, Claudio
Elevated IgM levels in a patient with a de novo 13Q12.3Q14.11 deletion, mimicking an A-T like phenotype
2012 Cirillo, Emilia; Romano, R.; Giardino, Giuliana; Anne, D.; Maio, F.; Gallo, Vera; Di Gregorio, E.; Cavalieri, S.; Abate, G.; DEL VECCHIO, Luigi; Brusco, A.; Pignata, Claudio
FOXN1: a master regulator gene of thymic epithelial development program
2013 Romano, Rosa; Palamaro, Loredana; Fusco, Anna; Giardino, Giuliana; Gallo, Vera; DEL VECCHIO, Luigi; Pignata, Claudio
Immunodeficienze primitive: cosa c’è di nuovo
2013 Cirillo, Emilia; Gallo, Vera; Giardino, Giuliana; Pignata, Claudio
FOXN1 in cell development and human diseases
2014 Palamaro, Loredana; Romano, Rosa; Fusco, A.; Giardino, Giuliana; Gallo, Vera; Pignata, Claudio
DiGeorge-like syndrome in a child with a 3p12.3 deletion involving miRNA-4273 born to a diabetic mother
2014 Cirillo, Emilia; Gallo, Vera; Giardino, Giuliana; Galasso, G.; Romano, R.; D'Assante, Roberta; Genesio, R.; Baldini, A.; Nitsch, Lucio; Pignata, Claudio
TLR9 signaling in patients with ectodermal dysplasia and immunodeficiency associated with Nuclear Factor Essential Modulator (NEMO) mutations
2014 Giardino, Giuliana; Naddei, Roberta; Cirillo, Emilia; Gallo, Vera; Esposito, T.; Fusco, F.; Quinti, I.; Ursini, M. V.; Carsetti, R.; Pignata, Claudio
Intrathecal amphotericin B therapy in a patient with X-linked chronic granulomatous disease and refractory cerebral invasive aspergillosis
2014 Gallo, Vera; Cirillo, Emilia; Giardino, Giuliana; D'Assante, Roberta; Spennato, P.; Cinalli, G.; Pignata, Claudio
Gastrointestinal involvement in patients affected with 22q11.2 deletion syndrome
2014 Giardino, Giuliana; Cirillo, Emilia; Maio, F.; Gallo, Vera; Esposito, T.; Naddei, Roberta; Grasso, F.; Pignata, Claudio
Chronic mucocutaneous candidiasis, recurrent herpetic infections and suppurative eyelid infections in a patient carrying a novel gain-of-function mutation in the STAT1 DNA-binding domain
2014 Giardino, Giuliana; Cirillo, Emilia; Gallo, Vera; D'Assante, Roberta; Paciolla, M.; Ruggiero, Giuseppina; Ursini, M. V.; Carsetti, R.; Puel, A.; Pignata, Claudio
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects
2014 Cirillo, Emilia; Giardino, Giuliana; Gallo, Vera; Puliafito, P.; Azzari, C.; Bacchetta, R.; Cardinale, F.; Cicalese, M. P.; Consolini, R.; Martino, S.; Martire, B.; Molinatto, C.; Plebani, A.; Scarano, G.; Soresina, A.; Cancrini, C.; Rossi, P.; Digilio, M. C.; Pignata, Claudio
Targeted next-generation sequencing revealed MYD88 deficiency in a child with chronic yersiniosis and granulomatous lymphadenitis
2015 Giardino, Giuliana; Gallo, Vera; Somma, Domenico; Farrow, Emily G; Thiffault, Isabelle; D'Assante, Roberta; Donofrio, Vittoria; Paciolla, Mariateresa; Ursini, Matilde Valeria; Leonardi, Antonio; Saunders, Carol J; Pignata, Claudio
Diagnostics of Primary immunodeficiencies through next-generation sequencing
2016 Gallo, Vera; Dotta, Laura; Giardino, Giuliana; Cirillo, Emilia; Lougaris, Vassilios; D'Assante, Roberta; Prandini, Alberto; Consolini, Rita; Farrow, Emily G.; Thiffault, Isabelle; Saunders, Carol J.; Leonardi, Antonio; Plebani, Alessandro; Badolato, Raffaele; Pignata, Claudio
A Bronchovascular Anomaly in a Patient With 22q11.2 Deletion Syndrome
2016 Romano, R; Cirillo, Emilia; Giardino, Giuliana; Gallo, Vera; Mollica, C; Pignata, Claudio
Phenotypic characterization and outcome of paediatric patients affected with haemophagocytic syndrome of unknown genetic cause.
2013 Giardino, Giuliana; Veropalumbo, C; Ruggiero, Giuseppina; Naddei, R; Rubino, Valentina; Udhayachandran, A; Cirillo, Emilia; Gallo, Vera; Poggi, V; De Fusco, C; Pignata, Claudio
FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
2017 Gallo, Vera; Cirillo, Emilia; Giardino, Giuliana; Pignata, Claudio
DiGeorge-like Syndrome in a Child with a 3p12.3 Deletion Involving MIR4273 Gene Born to a Mother with Gestational Diabetes Mellitus
2017 Cirillo, Emilia; Giardino, Giuliana; Gallo, Vera; Galasso, Giovanni; Romano, Roberta; D'Assante, Roberta; Scalia, Giulia; Vecchio, Luigi Del; Nitsch, Lucio; Genesio, Rita; Pignata, Claudio
Severe combined immunodeficiency-an update
2015 Cirillo, Emilia; Giardino, Giuliana; Gallo, Vera; D'Assante, Roberta; Grasso, Fiorentino; Romano, Roberta; Di Lillo, Cristina; Galasso, Giovanni; Pignata, Claudio
| Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|---|
| Intergenerational familial phenotipic variability in 22Q11.2 subjects: a multicenter study within the italian primary immunodeficiencies network (IPINET) | 1.5 Abstract in rivista | 2012 | Cirillo, Emilia; Giardino, Giuliana; Gallo, Vera; Puliafito, P.; Ariganello, P.; Azzari, C.; Cardinale, F.; Consolini, R.; Martino, S.; Plebani, A.; Scarano, G.; Soresina, A. R.; Cancrini, C.; Digilio, M. C.; Pignata, Claudio | |
| Evaluation of executive functions in subjects affected with 22Q11.2 deletion syndrome: a neuroanatomical hypothesis | 1.5 Abstract in rivista | 2012 | Marino, M.; Riccio, M. P.; Tiano, C.; Cirillo, Emilia; Maio, F.; Gallo, Vera; Esposito, T.; Roberta, N.; Pignata, Claudio; Bravaccio, Carmela | |
| Retrospective analysis of 21 pediatric patients affected with hemophagocytic syndrome of unknown genetic cause: clinical features and outcome | 1.5 Abstract in rivista | 2012 | Veropalumbo, C.; Giardino, Giuliana; Cirillo, Emilia; Gallo, Vera; Maio, F.; Esposito, T.; Naddei, R.; Grasso, F.; Poggi, V.; De Fusco, C.; Pignata, Claudio | |
| Elevated IgM levels in a patient with a de novo 13Q12.3Q14.11 deletion, mimicking an A-T like phenotype | 1.5 Abstract in rivista | 2012 | Cirillo, Emilia; Romano, R.; Giardino, Giuliana; Anne, D.; Maio, F.; Gallo, Vera; Di Gregorio, E.; Cavalieri, S.; Abate, G.; DEL VECCHIO, Luigi; Brusco, A.; Pignata, Claudio | |
| FOXN1: a master regulator gene of thymic epithelial development program | 1.1 Articolo in rivista | 2013 | Romano, Rosa; Palamaro, Loredana; Fusco, Anna; Giardino, Giuliana; Gallo, Vera; DEL VECCHIO, Luigi; Pignata, Claudio | |
| Immunodeficienze primitive: cosa c’è di nuovo | 1.1 Articolo in rivista | 2013 | Cirillo, Emilia; Gallo, Vera; Giardino, Giuliana; Pignata, Claudio | |
| FOXN1 in cell development and human diseases | 1.1 Articolo in rivista | 2014 | Palamaro, Loredana; Romano, Rosa; Fusco, A.; Giardino, Giuliana; Gallo, Vera; Pignata, Claudio | |
| DiGeorge-like syndrome in a child with a 3p12.3 deletion involving miRNA-4273 born to a diabetic mother | 1.5 Abstract in rivista | 2014 | Cirillo, Emilia; Gallo, Vera; Giardino, Giuliana; Galasso, G.; Romano, R.; D'Assante, Roberta; Genesio, R.; Baldini, A.; Nitsch, Lucio; Pignata, Claudio | |
| TLR9 signaling in patients with ectodermal dysplasia and immunodeficiency associated with Nuclear Factor Essential Modulator (NEMO) mutations | 1.5 Abstract in rivista | 2014 | Giardino, Giuliana; Naddei, Roberta; Cirillo, Emilia; Gallo, Vera; Esposito, T.; Fusco, F.; Quinti, I.; Ursini, M. V.; Carsetti, R.; Pignata, Claudio | |
| Intrathecal amphotericin B therapy in a patient with X-linked chronic granulomatous disease and refractory cerebral invasive aspergillosis | 1.5 Abstract in rivista | 2014 | Gallo, Vera; Cirillo, Emilia; Giardino, Giuliana; D'Assante, Roberta; Spennato, P.; Cinalli, G.; Pignata, Claudio | |
| Gastrointestinal involvement in patients affected with 22q11.2 deletion syndrome | 1.1 Articolo in rivista | 2014 | Giardino, Giuliana; Cirillo, Emilia; Maio, F.; Gallo, Vera; Esposito, T.; Naddei, Roberta; Grasso, F.; Pignata, Claudio | |
| Chronic mucocutaneous candidiasis, recurrent herpetic infections and suppurative eyelid infections in a patient carrying a novel gain-of-function mutation in the STAT1 DNA-binding domain | 1.5 Abstract in rivista | 2014 | Giardino, Giuliana; Cirillo, Emilia; Gallo, Vera; D'Assante, Roberta; Paciolla, M.; Ruggiero, Giuseppina; Ursini, M. V.; Carsetti, R.; Puel, A.; Pignata, Claudio | |
| Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects | 1.1 Articolo in rivista | 2014 | Cirillo, Emilia; Giardino, Giuliana; Gallo, Vera; Puliafito, P.; Azzari, C.; Bacchetta, R.; Cardinale, F.; Cicalese, M. P.; Consolini, R.; Martino, S.; Martire, B.; Molinatto, C.; Plebani, A.; Scarano, G.; Soresina, A.; Cancrini, C.; Rossi, P.; Digilio, M. C.; Pignata, Claudio | |
| Targeted next-generation sequencing revealed MYD88 deficiency in a child with chronic yersiniosis and granulomatous lymphadenitis | 1.1 Articolo in rivista | 2015 | Giardino, Giuliana; Gallo, Vera; Somma, Domenico; Farrow, Emily G; Thiffault, Isabelle; D'Assante, Roberta; Donofrio, Vittoria; Paciolla, Mariateresa; Ursini, Matilde Valeria; Leonardi, Antonio; Saunders, Carol J; Pignata, Claudio | |
| Diagnostics of Primary immunodeficiencies through next-generation sequencing | 1.1 Articolo in rivista | 2016 | Gallo, Vera; Dotta, Laura; Giardino, Giuliana; Cirillo, Emilia; Lougaris, Vassilios; D'Assante, Roberta; Prandini, Alberto; Consolini, Rita; Farrow, Emily G.; Thiffault, Isabelle; Saunders, Carol J.; Leonardi, Antonio; Plebani, Alessandro; Badolato, Raffaele; Pignata, Claudio | |
| A Bronchovascular Anomaly in a Patient With 22q11.2 Deletion Syndrome | 1.1 Articolo in rivista | 2016 | Romano, R; Cirillo, Emilia; Giardino, Giuliana; Gallo, Vera; Mollica, C; Pignata, Claudio | |
| Phenotypic characterization and outcome of paediatric patients affected with haemophagocytic syndrome of unknown genetic cause. | 1.1 Articolo in rivista | 2013 | Giardino, Giuliana; Veropalumbo, C; Ruggiero, Giuseppina; Naddei, R; Rubino, Valentina; Udhayachandran, A; Cirillo, Emilia; Gallo, Vera; Poggi, V; De Fusco, C; Pignata, Claudio | |
| FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches | 1.1 Articolo in rivista | 2017 | Gallo, Vera; Cirillo, Emilia; Giardino, Giuliana; Pignata, Claudio | |
| DiGeorge-like Syndrome in a Child with a 3p12.3 Deletion Involving MIR4273 Gene Born to a Mother with Gestational Diabetes Mellitus | 1.1 Articolo in rivista | 2017 | Cirillo, Emilia; Giardino, Giuliana; Gallo, Vera; Galasso, Giovanni; Romano, Roberta; D'Assante, Roberta; Scalia, Giulia; Vecchio, Luigi Del; Nitsch, Lucio; Genesio, Rita; Pignata, Claudio | |
| Severe combined immunodeficiency-an update | 1.1 Articolo in rivista | 2015 | Cirillo, Emilia; Giardino, Giuliana; Gallo, Vera; D'Assante, Roberta; Grasso, Fiorentino; Romano, Roberta; Di Lillo, Cristina; Galasso, Giovanni; Pignata, Claudio |