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Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis) 1-gen-1999 Iolascon, A; Stewart, Gw; Ajetunmobi, Jf; Perrotta, Silverio; Delaunay, J; Carella, M; Zelante, L; Gasparini, P.
Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndrome 1-gen-1999 Iolascon, A; Faienza, Mf; Giordani, L; Perrotta, Silverio; Ruggiu, G; Meloni, Gf; MIRAGLIA DEL GIUDICE, Emanuele
4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosis [3] 1-gen-1999 Perrotta, Silverio; Iolascon, A; Polito, R; D'Urzo, G; Conte, Ml; MIRAGLIA DEL GIUDICE, Emanuele
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
An autosomal dominant thrombocytopenia gene maps to chromosomal region 10p 1-gen-1999 Savoia, A; DEL VECCHIO, M; Totaro, A; Perrotta, Silverio; Amendola, G; Moretti, A; Zelante, L; Iolascon, A.
OSTEOPOROSIS IN THALASSEMIA MAJOR: EVALUATION OF GENETIC FACTORS 1-gen-1999 A., Iolascon; Iolascon, Giovanni; V., Servidio; Perrotta, Silverio; L., D'Agruma; P., Gasparini; C., DE ROSA; M. C., Siciliano; L., Danesi; M. D., Cappellini
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.
Osteoporosis in thalassema major: Evaluation of genetic factors. 1-gen-1999 Iolascon, A; Iolascon, Giovanni; Servidio, V; Perrotta, Silverio; D'Agruma, L; Gasparini, P; De Rosa, C; Siciliano, Mc; Danesi, L; Cappellini, Md
Familial dominant thrombocytopenia: clinical, biologic, and molecular studies 1-gen-1999 Iolascon, A; Perrotta, Silverio; Amendola, G; Altomare, M; Bagnara, Gp; DEL VECCHIO, Me; Savoia, 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.
Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II) 1-gen-2000 Perrotta, Silverio; DEL GIUDICE, Em; Carbone, R; Servedio, V; SCHETTINI F., Jr; Nobili, Bruno; Iolascon, A.
L1 effects on reactive oxygen (ROS) and nitrogen species (RNS) release, hemoglobin oxidation, low molecular weight antioxidants, and antioxidant enzyme activities in red and white blood cells of thalassemic patients 1-gen-2000 Korkina, L; DE LUCA, C; Deeva, I; Perrotta, Silverio; Nobili, Bruno; Passi, S; Puddu, P.
GILBERT'S SYNDROME ACCOUNTS FOR THE PHENOTYPIC VARIABILITY OF CDA-II 1-gen-2000 Perrotta, Silverio; MIRAGLIA DEL GIUDICE, Emanuele; Carbone, R.; Servedio, V.; Schettini, F.; Nobili, Bruno; Iolascon, A.
Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis 1-gen-2000 Tchernia, G; Delhommeau, F; Perrotta, Silverio; Cynober, T; BADER MEUNIER, B; Nobili, Bruno; Rohrlich, P; Salomon, Jl; SAGOT BEVENOT, S; DEL GIUDICE, Em; Delaunay, J; Demattia, D; Schischmanoff, Po; Mohandas, N; Iolascon, A; ESPHI WORKING GROUP ON HEMOLYTIC, Anemias
Geographic distribution of CDA-II: did a founder effect operate in Southern Italy? 1-gen-2000 Iolascon, A; Servedio, V; Carbone, R; Totaro, A; Carella, M; Perrotta, Silverio; Wickramasinghe, Sn; Delaunay, J; Heimpel, H; Gasparini, P.
ESPHI working group on hemolytic anemias. Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis 1-gen-2000 Tchernia, G; Delhommeau, F; Perrotta, Silverio; Cynober, T; BADER MEUNIER, B; Nobili, Bruno; Rohrlich, P; Salomon, Jl; SAGOT BEVENOT, S; MIRAGLIA DEL GIUDICE, Emanuele; Delaunay, J; Demattia, D; Schischmanoff, Po; Mohandas, N; Iolascon, A.
FREQUENCY OF GILBERT'S SYNDROME ASSOCIATED WITH UGTA1 (TA)(7) POLYMORPHISM IN SOUTHERN ITALY 1-gen-2000 Iolascon, A; Perrotta, Silverio; Coppola, B; Carbone, R; MIRAGLIA DEL GIUDICE, Emanuele
Osteoporosis in beta-thalassaemia major patients: analysis of the genetic background 1-gen-2000 Perrotta, Silverio; Cappellini, Md; Bertoldo, F; Servedio, V; Iolascon, Giovanni; D'Agruma, L; Gasparini, P; Siciliani, Mc; Iolascon, A.
Heavy transfusions and presence of an anti-protein 4.2 antibody in 4. 2(-) hereditary spherocytosis (949delG) 1-gen-2000 BEAUCHAMP NICOUD, A; Morle, L; Lutz, Hu; Stammler, P; Agulles, O; PETERMANN KHDER, R; Iolascon, A; Perrotta, Silverio; Cynober, T; Tchernia, G; Delaunay, J; BAUDIN CREUZA, V.
Clinical and molecular evaluation of non-dominant hereditary spherocytosis 1-gen-2001 MIRAGLIA DEL GIUDICE, Emanuele; Nobili, Bruno; Francese, M; D'Urso, L; Iolascon, A; Eber, S; Perrotta, Silverio
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