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Analysis of N-ras gene mutations in medulloblastomas by polymerase chain reaction and oligonucleotide probes in formalin-fixed, paraffin-embedded tissues 1-gen-1991 Iolascon, A; Lania, A; Badiali, M; Pession, A; Saglio, G; Giangaspero, F; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Cutillo, S.
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.
Hereditary spherocytosis characterized by increased spectrin/band 3 ratio 1-gen-1992 MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Pinto, L; Cappellini, Md; Fiorelli, G; Cutillo, S; Iolascon, A.
Alpha I/65 hereditary elliptocytosis in southern Italy: evidence for an African origin 1-gen-1992 MIRAGLIA DEL GIUDICE, Emanuele; Ducluzeau, Mt; Alloisio, N; Wilmotte, R; Delaunay, J; Perrotta, Silverio; Cutillo, S; Iolascon, A.
Hereditary spherocytosis (HS) due to loss of anion exchange transporter 1-gen-1992 Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Pinto, L; Fiorelli, G; Cappellini, Dm; Vasseur, C; Bursaux, E; Cutillo, S.
Severe poikilocytosis associated with a de novo alpha 28 Arg-->Cys mutation in spectrin 1-gen-1993 Lorenzo, F; MIRAGLIA DEL GIUDICE, Emanuele; Alloisio, N; Morle, L; Forissier, A; Perrotta, Silverio; Sciarratta, G; Iolascon, A; Delaunay, J.
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.
A rapid method for the detection of alpha I/65 hereditary elliptocytosis 1-gen-1993 Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Pinto, L; Cutillo, S.
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
Glucose 6-phosphate dehydrogenase deficiency and red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemia 1-gen-1994 Alfinito, F; Calabro, V; Cappellini, Md; Fiorelli, G; Filosa, S; Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Migliorati, R; Vallone, D.
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 deletional frameshift mutation in spectrin beta-gene associated with hereditary elliptocytosis in spectrin Napoli 1-gen-1994 Wilmotte, R; MIRAGLIA DEL GIUDICE, Emanuele; Marechal, J; Perrotta, Silverio; DE MATTIA, D; Delaunay, J; Iolascon, A.
Mild elliptocytosis associated with the alpha 34 Arg-->Trp mutation in spectrin Genova (alpha I/74) 1-gen-1994 Perrotta, Silverio; MIRAGLIA DEL GIUDICE, Emanuele; Alloisio, N; Sciarratta, G; Pinto, L; Delaunay, J; Cutillo, S; Iolascon, A.
Rapid detection of medium chain acyl-CoA dehydrogenase gene mutations by non-radioactive, single strand conformation polymorphism minigels 1-gen-1994 Iolascon, A; Parrella, T; Perrotta, Silverio; Guardamagna, O; Coates, Pm; Sartore, M; Surrey, S; Fortina, P.
Increased Membrane‐Protein Methylation in Hereditary Spherocytosis: A Marker of Cytoskeletal Disarray 1-gen-1995 Ingrosso, Diego; D'Angelo, S.; Perna, Alessandra; Iolascon, A.; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Zappia, V.; Galletti, P.
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.
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.
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
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
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