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p16INK4 gene deletions in childhood acute lymphoblastic leukemias 1-gen-1995 Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Russo, Gl; Oliva, Adriana; Mercurio, C; DELLA RAGIONE, Fulvio
Congenital dyserythropoietic anemia type II associated with G6PD Seattle in a Sicilian child 1-gen-1995 Gangarossa, S; Romano, V; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Iolascon, A; Schiliro, G.
Spectrin Anastasia (alpha I/78): a new spectrin variant (alpha 45 Arg-->Thr) with moderate elliptocytogenic potential 1-gen-1995 Perrotta, Silverio; Iolascon, A; DE ANGELIS, F; Pagano, L; Colonna, G; Cutillo, S; MIRAGLIA DEL GIUDICE, Emanuele
The Italian survey on hereditary spherocytosis 1-gen-1995 Pinto, L; Iolascon, A.; MIRAGLIA DEL GIUDICE, Emanuele; Matarese, S. M. R.; Nobili, B; Perrotta, S.
Ankyrin Napoli: a de novo deletional frameshift mutation in exon 16 of ankyrin gene (ANK1) associated with spherocytosis 1-gen-1996 MIRAGLIA DEL GIUDICE, Emanuele; Hayette, S; Bozon, M; Perrotta, Silverio; Alloisio, N; Vallier, A; Iolascon, A; Delaunay, J; Morlé, L.
The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulum 1-gen-1996 Alloisio, N; Texier, P; Denoroy, L; Berger, C; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Iolascon, A; Gilsanz, F; Berger, G; Guichard, J.
P16INK4A gene homozygous deletions in human acute leukaemias with alterations of chromosome 9 1-gen-1996 Faienza, Mf; DELLA RAGIONE, Fulvio; Basso, G; Coppola, B; MIRAGLIA DEL GIUDICE, Emanuele; Schettini, F; Iolascon, A.
Cytoskeletal behaviour in spectrin and in band 3 deficient spherocytic red cells: Evidence for a differentiated splenic conditioning role 1-gen-1996 Ingrosso, Diego; D'Angelo, S.; Perrotta, Silverio; D'Urzo, G.; Iolascon, A.; Perna, Alessandra; Galletti, P.; Zappia, V.; MIRAGLIA DEL GIUDICE, Emanuele
Congenital dyserythropoietic anemia type II: molecular basis and clinical aspects 1-gen-1996 Iolascon, A; D'Agostaro, G; Perrotta, Silverio; Izzo, P; Tavano, R; MIRAGLIA DEL GIUDICE, Emanuele
Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: effects of different membrane protein defects 1-gen-1997 DE FRANCESCHI, L; Olivieri, O; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Sabato, V; Corrocher, R; Iolascon, A.
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
Increased membrane protein phosphorylation and anion transport activity in chorea-acanthocytosis 1-gen-1997 Olivieri, O; DE FRANCESCHI, L; Bordin, L; Manfredi, M; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; DE VIVO, M; Guarini, P; Corrocher, R.
LOCALIZATION OF THE CONGENITAL DYSERYTHROPOIETIC ANEMIA II LOCUS TO CHROMOSOME 20Q11.2 BY GENOMEWIDE SEARCH 1-gen-1997 Gasparini, P; MIRAGLIA DEL GIUDICE, Emanuele; Delaunay, J; Totaro, A; Granatiero, M; Melchionda, S; Zelante, L; Iolascon, A.
Novel band 3 variants (bands 3 Foggia, Napoli I and Napoli II) associated with hereditary spherocytosis and band 3 deficiency: status of the D38A polymorphism within the EPB3 locus 1-gen-1997 MIRAGLIA DEL GIUDICE, Emanuele; Vallier, A; Maillet, P; Perrotta, Silverio; Cutillo, S; Iolascon, A; Tanner, Mj; Delaunay, J; Alloisio, N.
Frequent de novo mutations of the ANK1 gene mimic a recessive mode of transmission in hereditary spherocytosis: three new ANK1 variants: ankyrins Bari, Napoli II and Anzio 1-gen-1997 Randon, J; MIRAGLIA DEL GIUDICE, Emanuele; Bozon, M; Perrotta, Silverio; DE VIVO, M; Iolascon, A; Delaunay, J; Morle, L.
Exclusion of three candidate genes as determinants of congenital dyserythropoietic anemia type II (CDA-II) 1-gen-1997 Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Granatiero, M; Zelante, L; Gasparini, P.
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
Obesità nell'età evolutiva: ruolo della leptina 1-gen-1998 Perrone, Laura; MIRAGLIA DEL GIUDICE, Emanuele; DI TORO, R.
UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis 1-gen-1998 Iolascon, A; Faienza, Mf; Moretti, A; Perrotta, Silverio; MIRAGLIA DEL GIUDICE, Emanuele
DECISION MAKING AT THE BEDSIDE: DIAGNOSIS OF HEREDITARY SPHEROCYTOSIS IN A TRANSFUSED INFANT 1-gen-1998 MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Lombardi, C; Iolascon, A.
Mostrati risultati da 21 a 40 di 419
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