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Haematologica|May 1, 1997
Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) alleleE Miraglia del Giudice, M Francese, R Polito, et al.
British Journal of Haematology|February 13, 2001
Clinical and molecular evaluation of non-dominant hereditary spherocytosisE Miraglia del Giudice, B Nobili, M Francese, et al.
European Journal of Biochemistry|September 1, 1983
Increased methyl esterification of membrane proteins in aged red-blood cells. Preferential esterification of ankyrin and band-4.1 cytoskeletal proteinsP Galletti, D Ingrosso, A Nappi, et al.
British Journal of Haematology|September 1, 1994
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosisE Miraglia del Giudice, A Iolascon, L Pinto, et al.
European Journal of Pediatrics|January 1, 1992
Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosisS Cutillo, L Pinto, B Nobili, et al.
Human Genetics|January 1, 1985
Genetic heterogeneity at the glucose-6-phosphate dehydrogenase locus in southern Italy: a study on the population of NaplesS Colonna-Romano, A Iolascon, S Lippo, et al.
British Journal of Haematology|November 1, 1993
Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotypeE Miraglia del Giudice, S Perrotta, B Nobili, et al.
British Journal of Haematology|June 3, 1998
Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiencyE Miraglia del Giudice, C Lombardi, M Francese, et al.
British Journal of Haematology|August 1, 1991
Ankyrin deficiency in dominant hereditary spherocytosis: report of three casesA Iolascon, E Miraglia del Giudice, C Camaschella, et al.
Blood|June 1, 1994
Mild elliptocytosis associated with the alpha 34 Arg-->Trp mutation in spectrin Genova (alpha I/74)S Perrotta, E Miraglia del Giudice, N Alloisio, et al.
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