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Developmental changes in HbA2 and HbF on neocytes and gerocytes in normal infants during the first year of life 1-gen-1983 Iolascon, A; Pinto, L; Nobili, Bruno; Cutillo, S.
Campylobacter enteritis: an emerging disease 1-gen-1983 Pinto, L; Alagia, I; Imparato, P; Iolascon, A; Iolascon, Giovanni; Nappi, R; Nobili, Bruno
Clinical and biochemical study of thalassemia intermedia in Campania (southern Italy) 1-gen-1987 Iolascon, A; Pinto, L; Nobili, Bruno; Lania, A; Iafusco, Dario; MIRAGLIA DEL GIUDICE, Emanuele; Matarese, Sm; Salvati, P; Cutillo, S.
A modification of the 'pink test' may improve the diagnosis of hereditary spherocytosis 1-gen-1989 Pinto, L; Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Nobili, Bruno
Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases 1-gen-1991 Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Camaschella, C; Pinto, L; Nobili, Bruno; Perrotta, Silverio; Cutillo, S.
Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis 1-gen-1992 Cutillo, S; Pinto, L; Nobili, Bruno; MIRAGLIA DEL GIUDICE, Emanuele; Iolascon, A.
Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotype 1-gen-1993 MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Nobili, Bruno; Pinto, L; Cutillo, L; Iolascon, A.
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis 1-gen-1994 MIRAGLIA DEL GIUDICE, Emanuele; Iolascon, A; Pinto, L; Nobili, Bruno; Perrotta, Silverio
La prevenzione dell’anemia mediterranea in Campania: stato attuale e prospettive 1-gen-1994 Carestia, C; De Angioletti, M; Lacerra, G; Fioretti, G; Pagano, L; De Rosa, C; Di Girolamo, R; Sciorio, A; De Biase, R; Mastrullo, L; Colella, R; Vaccaro, E; Friggino, M; Rinaldi, C; Di Lonardo, A; Nobili, Bruno; Francese, M; Danise, P; Amendola, G; Guastafierro, Salvatore; D’Onofrio, R.
Molecular heterogeneity of hereditary elliptocytosis in Italy 1-gen-1994 MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Sannino, E; DE ANGELIS, F; Nobili, Bruno; Iolascon, A.
A trial of high-dose dexamethasone therapy for chronic idiopathic thrombocytopenic purpura in childhood 1-gen-1997 BORGNA PIGNATTI, C; Rugolotto, S; Nobili, Bruno; Amendola, G; DE STEFANO, P; Maccario, R; Locatelli, F.
Diamond-Blackfan anemia: expansion of erythroid progenitors in vitro by IL-9, but exclusion of a significant pathogenetic role for the IL-9 gene and the hematopoietic gene cluster on chromosome 5q 1-gen-1997 Dianzani, I; Garelli, E; Crescenzio, N; Timeus, F; Mori, Pg; Varotto, S; Nobili, Bruno; Brandalise, S; Olivieri, Nf; Gabutti, V; Ramenghi, U.
Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele 1-gen-1997 MIRAGLIA DEL GIUDICE, Emanuele; Francese, M; Polito, R; Nobili, Bruno; Iolascon, A; Perrotta, Silverio
High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis 1-gen-1998 MIRAGLIA DEL GIUDICE, Emanuele; Francese, M; Nobili, Bruno; Morle, L; Cutillo, S; Delaunay, J; Perrotta, Silverio
Terapia con rHu Epo in un caso di diabete mellito “early onset” ed anemia aplastica normocitica 1-gen-1998 Nobili, Bruno; Prisco, F; Stoppoloni, O; Iafusco, Dario; Matarese, Smr; D’Urzo, G.
Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency 1-gen-1998 MIRAGLIA DEL GIUDICE, Emanuele; Lombardi, C; Francese, M; Nobili, Bruno; Conte, Ml; Amendola, G; Cutillo, S; Iolascon, A; Perrotta, Silverio
Diamond-Blackfan anaemia in the Italian population 1-gen-1999 Ramenghi, U; Garelli, E; Valtolina, S; Campagnoli, Mf; Timeus, F; Crescenzio, N; Mair, M; Varotto, S; D'Avanzo, M; Nobili, Bruno; Massolo, F; Mori, Pg; Locatelli, F; Gustavsson, P; Dahl, N; Dianzani, I.
Hereditary spherocytosis due to a novel frameshift mutation in AE1 cytoplasmic COOH terminal tail: band 3 Vesuvio 1-gen-1999 Perrotta, Silverio; Polito, F; Cone, Ml; Nobili, Bruno; Cutillo, S; Nigro, Vincenzo; Iolascon, A; Amendola, G; MIRAGLIA DEL GIUDICE, Emanuele
COINHERITANCE OF GILBERT SYNDROME INCREASES THE RISK FOR DEVELOPING GALLSTONES IN PATIENTS WITH HEREDITARY SPHEROCYTOSIS 1-gen-1999 MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Nobili, Bruno; Specchia, C; D'Urzo, G; Iolascon, A.
Le anemie diseritropoietiche 1-gen-1999 Iolascon, A; Servedio, V; Moretti, A; Carbone, R; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Nobili, Bruno; Gasparini, P.
Mostrati risultati da 21 a 40 di 120
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