IRIS

Sfoglia per Autore  

Opzioni
Mostrati risultati da 41 a 60 di 419
Titolo Data di pubblicazione Autore(i) File
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
Hereditary spherocytosis: from clinical to molecular defects 1-gen-1998 Iolascon, A; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Alloisio, N; Morlé, L; Delaunay, J.
Leptin level and structure in Italian obese children 1-gen-1998 Perrone, Laura; Carbone, Mt; Marotta, A; Palombo, G; Francese, M; Cioffi, Michele; MIRAGLIA DEL GIUDICE, Emanuele
Decreased band 3 anion transport activity and band 3 clusterization in congenital dyserythropoietic anemia type II 1-gen-1998 DE FRANCESCHI, L; Turrini, F; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Olivieri, O; Corrocher, R; Mannu, F; Iolascon, A.
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
Le anemie diseritropoietiche 1-gen-1999 Iolascon, A; Servedio, V; Moretti, A; Carbone, R; MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Nobili, Bruno; Gasparini, P.
Evaluation of leptin protein levels in patients with Cooley's anaemia 1-gen-1999 MIRAGLIA DEL GIUDICE, Emanuele; Perrotta, Silverio; Carbone, Mt; Calabro, C; Esposito, L; DE ROSA, C; Saviano, A; DI TORO, R; Perrone, Laura
uppression of CDA II expression in a homozygote 1-gen-1999 BEAUCHAMP NICOUD, A; Schischmanoff, Po; Alloisio, N; Boivin, P; Parsons, Sf; Mielot, F; Tchernia, G; Legrand, A; MIRAGLIA DEL GIUDICE, Emanuele; Gasparini, P; Iolascon, A; Wickramasinghe, Sn; Delaunay, J
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.
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
Gilbert's syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonates 1-gen-1999 Iolascon, A; Faienza, Mf; Perrotta, Silverio; Meloni, Gf; Ruggiu, G; MIRAGLIA DEL GIUDICE, Emanuele
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
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.
Mutazioni delle regioni core-promoter e pre-core di HBV in pazienti con pregressa malattia oncologica affetti da epatite cronica B prima, durante e dopo trattamento con interferone 1-gen-2000 Zampino, Rosa; Marrone, Aldo; G., Cirillo; MIRAGLIA DEL GIUDICE, Emanuele; P., Bellopede; A., Andreana; M., Marracino; Utili, Riccardo; P., Karayannis; G., Ruggiero
Sequential analysis of HBV core promoter and precore regions in cancer survivor patients with chronic hepatitis B before, during and after interferon treatment. 1-gen-2000 Zampino, Rosa; Marrone, Aldo; Cirillo, G; MIRAGLIA DEL GIUDICE, Emanuele; Bellopede, P; Andreana, A; Marracino, M; Utili, Riccardo; Karayiannis, P; Ruggiero, G.
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
Linkage study of early-onset obesity to leptin receptor gene in Italian children 1-gen-2000 MIRAGLIA DEL GIUDICE, Emanuele; Perrone, Laura; Carbone, Mt; Di Toro, R.
Benign familial neonatal convulsions (BFNC) resulting from mutation of the KCNQ2 voltage sensor 1-gen-2000 MIRAGLIA DEL GIUDICE, Emanuele; Coppola, G; Scuccimarra, G; Cirillo, G; Bellini, Giulia; Pascotto, Antonio
Mostrati risultati da 41 a 60 di 419
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile