Sfoglia per Autore
Congenital dyserythropoietic anemia type II: exclusion of seven candidate genes.
2003-01-01 Lanzara, C; Ficarella, R; Totaro, A; Chen, X; Roberto, R; Perrotta, S; Lasalandra, C; Gasparini, P; Iolascon, Achille; Carella, M.
Inheredited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle piastrine
2003-01-01 Balduini, C; Cattaneo, M; Fabris, F; Gresele, P; Iolascon, Achille; Pulcinelli, F; Savoia, A.
Anemia diseritopoietica congenitas
2003-01-01 Iolascon, Achille
Incidence and outcome of hospital acquired malnutrition in children.
2003-01-01 Campanozzi, A; Tummolo, A; Rutigliano, I; Nigro, A; Alberghini, V; D'Ademo, D; Romondia, A; Iolascon, A
Red blood cell membrane defects Rev.
2003-01-01 Iolascon, Achille; PERROTTA S., AND GW STEWART
Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1.
2005-01-01 Bruce, Lj; Robinson, Hc; Guizouarn, H; Borgese, F; Harrison, P; King, Mj; Goede, Js; Coles, Se; Gore, Dm; Lutz, Hu; Ficarella, R; Layton, Dm; Iolascon, Achille; Ellory, Jc; Stewart, Gw
Spectrum of UGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlation.
2005-01-01 Servedio, V; D'Apolito, M; Maiorano, N; Minuti, B; Torricelli, F; Ronchi, F; Zancan, L; Perrotta, S; P., Vajro; Boschetto, L; Iolascon, Achille
Erythroid membrane proteomic
2005-01-01 Orrù, S.; Caterino, M.; Ruoppolo, M.; Savoia, M.; Perrotta, S.; Salvatore, F.; Iolascon, Achille
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Congenital dyserythropoietic anemia type II: exclusion of seven candidate genes. | 1-gen-2003 | Lanzara, C; Ficarella, R; Totaro, A; Chen, X; Roberto, R; Perrotta, S; Lasalandra, C; Gasparini, P; Iolascon, Achille; Carella, M. | |
| Inheredited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle piastrine | 1-gen-2003 | Balduini, C; Cattaneo, M; Fabris, F; Gresele, P; Iolascon, Achille; Pulcinelli, F; Savoia, A. | |
| Anemia diseritopoietica congenitas | 1-gen-2003 | Iolascon, Achille | |
| Incidence and outcome of hospital acquired malnutrition in children. | 1-gen-2003 | Campanozzi, A; Tummolo, A; Rutigliano, I; Nigro, A; Alberghini, V; D'Ademo, D; Romondia, A; Iolascon, A | |
| Red blood cell membrane defects Rev. | 1-gen-2003 | Iolascon, Achille; PERROTTA S., AND GW STEWART | |
| Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1. | 1-gen-2005 | Bruce, Lj; Robinson, Hc; Guizouarn, H; Borgese, F; Harrison, P; King, Mj; Goede, Js; Coles, Se; Gore, Dm; Lutz, Hu; Ficarella, R; Layton, Dm; Iolascon, Achille; Ellory, Jc; Stewart, Gw | |
| Spectrum of UGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlation. | 1-gen-2005 | Servedio, V; D'Apolito, M; Maiorano, N; Minuti, B; Torricelli, F; Ronchi, F; Zancan, L; Perrotta, S; P., Vajro; Boschetto, L; Iolascon, Achille | |
| Erythroid membrane proteomic | 1-gen-2005 | Orrù, S.; Caterino, M.; Ruoppolo, M.; Savoia, M.; Perrotta, S.; Salvatore, F.; Iolascon, Achille |
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