Sfoglia per ???browse.type.metadata.subjectIsicrui??? Pediatria
WALKER'S PEDIATRIC GASTROINTESTINAL DISEASE, 6TH
2017-01-01 Nobili, V; Iasevoli, S; Villani, A
Waning of vaccine-induced immunity to measles in kidney transplanted children
2016-01-01 Rocca, S; Santilli, V; Cotugno, N; Concato, C; Manno, E; Nocentini, G; Macchiarulo, G; Cancrini, C; Finocchi, A; Guzzo, I; Strologo, L; Palma, P
When an induced illness looks like a rare disease.
2015-01-01 Rabbone, I; Galderisi, A; Tinti, D; Ignaccolo, M; Barbetti, F; Cerutti, F
Whole exome sequencing approach to childhood onset familial erythrodermic psoriasis unravels a novel mutation of CARD14 requiring unusual high doses of ustekinumab
2019-01-01 Signa, S; Campione, E; Rusmini, M; Chiesa, S; Grossi, A; Omenetti, A; Caorsi, R; Viglizzo, Gm; Galluzzo, M; Bianchi, L; Talamonti, M; Orlandi, A; Martini, A; Ceccherini, I; Gattorno, M
Williams syndrome and growth hormone deficiency
1983-01-01 Spadoni, G; Colloridi, V; Finocchi, G; MANCA BITTI, Ml; Chini, L; Boscherini, B
X-chromosome inactivation and mutation pattern in the Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinemia. Italian XLA Collaborative Group
2000-02-01 Moschese, V; Orlandi, P; Plebani, A; Arvanitidis, K; Fiorini, M; Speletas, M; Mella, P; Ritis, K; Sideras, P; Finocchi, A; Livadiotti, S; Rossi, P
X-linked agammaglobulinemia (XLA): An Italian Multicenter Clinical Study
1998-01-01 Plebani, A; Baldassarre, M; Cardinale, F; Cazzola, G; De Mattia, D; Duse, M; Flore, M; Martino, S; Masi, M; Monafo, V; Pietrogrande, C; Pignata, C; Quinti, I; Ragno, V; Rossi, P; Stabile, A; Moschese, V
| Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 1-gen-2017 | WALKER'S PEDIATRIC GASTROINTESTINAL DISEASE, 6TH | Nobili, V; Iasevoli, S; Villani, A | Contributo in libro | |
| 1-gen-2016 | Waning of vaccine-induced immunity to measles in kidney transplanted children | Rocca, S; Santilli, V; Cotugno, N; Concato, C; Manno, E; Nocentini, G; Macchiarulo, G; Cancrini, C; Finocchi, A; Guzzo, I; Strologo, L; Palma, P | Articolo su rivista | |
| 1-gen-2015 | When an induced illness looks like a rare disease. | Rabbone, I; Galderisi, A; Tinti, D; Ignaccolo, M; Barbetti, F; Cerutti, F | Articolo su rivista | |
| 1-gen-2019 | Whole exome sequencing approach to childhood onset familial erythrodermic psoriasis unravels a novel mutation of CARD14 requiring unusual high doses of ustekinumab | Signa, S; Campione, E; Rusmini, M; Chiesa, S; Grossi, A; Omenetti, A; Caorsi, R; Viglizzo, Gm; Galluzzo, M; Bianchi, L; Talamonti, M; Orlandi, A; Martini, A; Ceccherini, I; Gattorno, M | Articolo su rivista | |
| 1-gen-1983 | Williams syndrome and growth hormone deficiency | Spadoni, G; Colloridi, V; Finocchi, G; MANCA BITTI, Ml; Chini, L; Boscherini, B | Articolo su rivista | |
| 1-feb-2000 | X-chromosome inactivation and mutation pattern in the Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinemia. Italian XLA Collaborative Group | Moschese, V; Orlandi, P; Plebani, A; Arvanitidis, K; Fiorini, M; Speletas, M; Mella, P; Ritis, K; Sideras, P; Finocchi, A; Livadiotti, S; Rossi, P | Articolo su rivista | |
| 1-gen-1998 | X-linked agammaglobulinemia (XLA): An Italian Multicenter Clinical Study | Plebani, A; Baldassarre, M; Cardinale, F; Cazzola, G; De Mattia, D; Duse, M; Flore, M; Martino, S; Masi, M; Monafo, V; Pietrogrande, C; Pignata, C; Quinti, I; Ragno, V; Rossi, P; Stabile, A; Moschese, V | Articolo su rivista |
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