SCHETTINI, Federico
SCHETTINI, Federico
DIPARTIMENTO INTERDISCIPLINARE DI MEDICINA
14q13 distal microdeletion encompassing NKX2-1 and PAX9: Patient report and refinement of the associated phenotype
2016-01-01 Gentile, Mattia; DE MATTIA, Delia; Pansini, Angela; Schettini, Federico; Buonadonna, Antonia Lucia; Capozza, Manuela; Ficarella, Romina; Laforgia, Nicola
A case of fetal midgut volvulus and jejunal atresia: nutritional support and maintenance of mucosal function and integrity
2008-01-01 Baldassarre, Maria Elisabetta; Laneve, A; Rizzo, A; DI LEO, Alfredo; Schettini, Federico; Filannino, A; Laforgia, Nicola
Abdominal aorta vascular wall changes in healthy term neonates induced by their own and mothers cardiovascular risk factors
2012-01-01 Ciccone, Marco Matteo; P., Scicchitano; M., Gesualdo; F., Fornarelli; Zito, Annapaola; F., Giardinelli; F., Pini; DI MAURO, Antonio; F., Schettini; Laforgia, Nicola
Afibrinogenemia congenita associata a deficit di PC K-dipendente
1991-01-01 De Mattia, D; Regina, G; Giordano, Paola; Del Vecchio, G; Altomare, Maria; Schettini, F.
Afibrinogenemia congenita associata a deficit di PC K-dipendente
1991-01-01 De Mattia, D; Regina, G; Giordano, Paola; Del Vecchio, Gc; Altomare, Maria; Schettini, F.
Age and dose related urinary iron excretion by subcutaneous infusions of deferoxamine in thalassemia major children
1979-01-01 Schettini, F; Mautone, A; Marvulli, E; Altomare, Maria; Licciulli, M; Vurro, F.
Alterazioni immunologiche in bambini con emofilia
1984-01-01 De Mattia, D; Trupo, S; Ciavarella, G; Altomare, Maria; Ciavarella, N; Parato, M; Valori, Vm; Carotenuto, M; Schettini, F.
ALTERAZIONI ORO-FACCIALI NELLA TALASSEMIA MAJOR
1995-01-01 DE MATTIA, D.; Pettini, P. SABATO V.; Rubini, Giuseppe; Laforgia, Alessandra; Schettini, F.
Analysis of cyclin-dependent kinase inhibitor genes (CDKN2A, CDKN2B, and CDKN2C) in childhood rhabdomyosarcoma
1996-01-01 Iolascon, A; Faienza, Maria Felicia; Coppola, B; Rosolen, A; Basso, G; Della Ragione, F; Schettini, F.
Aorta structural alterations in term neonates: the role of birth and maternal characteristics.
2013-01-01 Ciccone, Marco Matteo; Scicchitano, Pietro; Salerno, C; Gesualdo, Michele; Fornarelli, Fara; Zito, Annapaola; Filippucci, L; Riccardi, R; Cortese, Francesca; Pini, F; Angrisani, L; DI MAURO, Antonio; Schettini, Federico; Laforgia, Nicola
APC resistance in thalassemic patients
1997-01-01 Giordano, Paola; Sabato, V; Del Vecchio, Gc; Altomare, Maria; Coppola, I; Iolascon, A; Schettini, F; De Mattia, D.
APC Resistance in thalassemic patients and under-lying cause of thrombosis
1997-01-01 DE MATTIA, D; Giordano, Paola; DEL VECCHIO, Gc; Schettini, Federico; Coppola, I; Altomare, Maria; Schettini, F.
APC resistance in thalassemic patients:an under-lying cause of thrombosis
1997-01-01 De Mattia, D; Giordano, Paola; Sabato, V; Schettini F., Jr; Coppola, I; Altomare, Maria; Schettini, F.
Association of congenital afibrinogenemia and k-dependent protein C deficiency - a case report
1993-01-01 De Mattia, D; Regina, G; Giordano, Paola; Del Vecchio, Gc; Altomare, Maria; Schettini, F.
Benign lymphoproliferation syndrome, autoimmune neutropenia and thrombocytopenia in partial Di George syndrome: efficacy of rh G-CSF and prednisone
2001-01-01 Martire, B; Burattini, Mg; DE SANTIS, A; Schettini, Federico; DE MATTIA, D.
Benign lymphoproliferation syndrome, autoimmune neutropenia and thrombocytopenia in partial Di George syndrome: efficacy of rh G-CSF and prednisone
2001-01-01 Martire, B; Burattini, M G; De Santis, A; Schettini, F; De Mattia, D
Bone marrow transplantation for chronic granulomatous disease associated with cytochrome b deficiency
1987-01-01 F., Schettini; D., DE MATTIA; M. M., Manzionna; R. A., Seger; Fumarulo, Ruggiero; G., Torlontano; A., Iacone
Cellular and plasmatic anomalies of the coagulation system and fibrinolysis in children with lymphomas and influence of cytostatic treatment
1993-01-01 De Mattia, D; Giordano, Paola; Montemurro, Pasqualina; Santoro, N; Colucci, Mario; Semeraro, N; Schettini, F.
CGD associated with cytochrome b deficiency: granulocyte function tests 25 months after bone marrow transplantation
1988-01-01 M. M., Manzionna; D., DE MATTIA; Fumarulo, Ruggiero; G., Torlontano; F., Schettini
Chronic cough and bronchial hyper-reactivity in children with mycoplasma and chlamidia pneumoniae infection
1999-01-01 Mappa, L; Loiodice, A; Nigro, A; Mangione, M; Schettini, Federico; Camedoca, R; Rigillo, N
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 14q13 distal microdeletion encompassing NKX2-1 and PAX9: Patient report and refinement of the associated phenotype | 1-gen-2016 | Gentile, Mattia; DE MATTIA, Delia; Pansini, Angela; Schettini, Federico; Buonadonna, Antonia Lucia; Capozza, Manuela; Ficarella, Romina; Laforgia, Nicola | |
| A case of fetal midgut volvulus and jejunal atresia: nutritional support and maintenance of mucosal function and integrity | 1-gen-2008 | Baldassarre, Maria Elisabetta; Laneve, A; Rizzo, A; DI LEO, Alfredo; Schettini, Federico; Filannino, A; Laforgia, Nicola | |
| Abdominal aorta vascular wall changes in healthy term neonates induced by their own and mothers cardiovascular risk factors | 1-gen-2012 | Ciccone, Marco Matteo; P., Scicchitano; M., Gesualdo; F., Fornarelli; Zito, Annapaola; F., Giardinelli; F., Pini; DI MAURO, Antonio; F., Schettini; Laforgia, Nicola | |
| Afibrinogenemia congenita associata a deficit di PC K-dipendente | 1-gen-1991 | De Mattia, D; Regina, G; Giordano, Paola; Del Vecchio, G; Altomare, Maria; Schettini, F. | |
| Afibrinogenemia congenita associata a deficit di PC K-dipendente | 1-gen-1991 | De Mattia, D; Regina, G; Giordano, Paola; Del Vecchio, Gc; Altomare, Maria; Schettini, F. | |
| Age and dose related urinary iron excretion by subcutaneous infusions of deferoxamine in thalassemia major children | 1-gen-1979 | Schettini, F; Mautone, A; Marvulli, E; Altomare, Maria; Licciulli, M; Vurro, F. | |
| Alterazioni immunologiche in bambini con emofilia | 1-gen-1984 | De Mattia, D; Trupo, S; Ciavarella, G; Altomare, Maria; Ciavarella, N; Parato, M; Valori, Vm; Carotenuto, M; Schettini, F. | |
| ALTERAZIONI ORO-FACCIALI NELLA TALASSEMIA MAJOR | 1-gen-1995 | DE MATTIA, D.; Pettini, P. SABATO V.; Rubini, Giuseppe; Laforgia, Alessandra; Schettini, F. | |
| Analysis of cyclin-dependent kinase inhibitor genes (CDKN2A, CDKN2B, and CDKN2C) in childhood rhabdomyosarcoma | 1-gen-1996 | Iolascon, A; Faienza, Maria Felicia; Coppola, B; Rosolen, A; Basso, G; Della Ragione, F; Schettini, F. | |
| Aorta structural alterations in term neonates: the role of birth and maternal characteristics. | 1-gen-2013 | Ciccone, Marco Matteo; Scicchitano, Pietro; Salerno, C; Gesualdo, Michele; Fornarelli, Fara; Zito, Annapaola; Filippucci, L; Riccardi, R; Cortese, Francesca; Pini, F; Angrisani, L; DI MAURO, Antonio; Schettini, Federico; Laforgia, Nicola | |
| APC resistance in thalassemic patients | 1-gen-1997 | Giordano, Paola; Sabato, V; Del Vecchio, Gc; Altomare, Maria; Coppola, I; Iolascon, A; Schettini, F; De Mattia, D. | |
| APC Resistance in thalassemic patients and under-lying cause of thrombosis | 1-gen-1997 | DE MATTIA, D; Giordano, Paola; DEL VECCHIO, Gc; Schettini, Federico; Coppola, I; Altomare, Maria; Schettini, F. | |
| APC resistance in thalassemic patients:an under-lying cause of thrombosis | 1-gen-1997 | De Mattia, D; Giordano, Paola; Sabato, V; Schettini F., Jr; Coppola, I; Altomare, Maria; Schettini, F. | |
| Association of congenital afibrinogenemia and k-dependent protein C deficiency - a case report | 1-gen-1993 | De Mattia, D; Regina, G; Giordano, Paola; Del Vecchio, Gc; Altomare, Maria; Schettini, F. | |
| Benign lymphoproliferation syndrome, autoimmune neutropenia and thrombocytopenia in partial Di George syndrome: efficacy of rh G-CSF and prednisone | 1-gen-2001 | Martire, B; Burattini, Mg; DE SANTIS, A; Schettini, Federico; DE MATTIA, D. | |
| Benign lymphoproliferation syndrome, autoimmune neutropenia and thrombocytopenia in partial Di George syndrome: efficacy of rh G-CSF and prednisone | 1-gen-2001 | Martire, B; Burattini, M G; De Santis, A; Schettini, F; De Mattia, D | |
| Bone marrow transplantation for chronic granulomatous disease associated with cytochrome b deficiency | 1-gen-1987 | F., Schettini; D., DE MATTIA; M. M., Manzionna; R. A., Seger; Fumarulo, Ruggiero; G., Torlontano; A., Iacone | |
| Cellular and plasmatic anomalies of the coagulation system and fibrinolysis in children with lymphomas and influence of cytostatic treatment | 1-gen-1993 | De Mattia, D; Giordano, Paola; Montemurro, Pasqualina; Santoro, N; Colucci, Mario; Semeraro, N; Schettini, F. | |
| CGD associated with cytochrome b deficiency: granulocyte function tests 25 months after bone marrow transplantation | 1-gen-1988 | M. M., Manzionna; D., DE MATTIA; Fumarulo, Ruggiero; G., Torlontano; F., Schettini | |
| Chronic cough and bronchial hyper-reactivity in children with mycoplasma and chlamidia pneumoniae infection | 1-gen-1999 | Mappa, L; Loiodice, A; Nigro, A; Mangione, M; Schettini, Federico; Camedoca, R; Rigillo, N |