Elevated levels of plasma triglycerides are associated with histologically defined premenopausal breast cancer risk
Goodwin, P J, Boyd, N F, Hanna, W, Hartwick, W, Murray, D, Qizilbash, A, Redwood, S, Hood, N, DelGiudice, M E, Sidlofsky, S, McCready, D, Wilkinson, R, Mahoney, L, Connelly, P, Page, D L
Published in Nutrition and cancer (1997)
Published in Nutrition and cancer (1997)
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Localization of the Congenital Dyserythropoietic Anemia II Locus to Chromosome 20q11.2 by Genomewide Search
Gasparini, P., Miraglia del Giudice, E., Delaunay, J., Totaro, A., Granatiero, M., Melchionda, S., Zelante, L., Iolascon, A.
Published in American journal of human genetics (01.11.1997)
Published in American journal of human genetics (01.11.1997)
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Journal Article
Congenital dyserythropoietic anemia type II: molecular basis and clinical aspects
Iolascon, A, D'Agostaro, G, Perrotta, S, Izzo, P, Tavano, R, Miraglia del Giudice, B
Published in Haematologica (Roma) (01.11.1996)
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Published in Haematologica (Roma) (01.11.1996)
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The Cisternae Decorating the Red Blood Cell Membrane in Congenital Dyserythropoietic Anemia (Type II) Originate From the Endoplasmic Reticulum
Alloisio, N., Texier, P., Denoroy, L., Berger, C., Giudice, E.Miraglia del, Perrotta, S., lolascon, A., Gilsanz, F., Berger, G., Guichard, J., Masse, J.M., Debili, N., Breton-Gorius, J., Delaunay, J.
Published in Blood (15.05.1996)
Published in Blood (15.05.1996)
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Attitudes of Canadian Oncology Practitioners Toward Psychosocial Interventions in Clinical and Research Settings in Women With Breast Cancer
Del Giudice, M. Elizabeth, Leszcz, Molyn, Pritchard, Kathleen I., Vincent, Leslie, Goodwin, Pamela
Published in Psycho-oncology (Chichester, England) (01.09.1997)
Published in Psycho-oncology (Chichester, England) (01.09.1997)
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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
RANDON, J., MIRAGLIA DEL GIUDICE, E., BOZON, M., PERROTTA, S., DE VIVO, M., IOLASCON, A., DELAUNAY, J., MORLE, L.
Published in British journal of haematology (01.03.1997)
Published in British journal of haematology (01.03.1997)
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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
MIRAGLIA del GIUDICE, Emanuele, VALLIER, AgnÉs, MAILLET, Philippe, PERROTTA, Silverio, CUTILLO, Stefano, IOLASCON, Achille, TANNER, Michael J. A., DELAUNAY, Jean, ALLOISIO, Nicole
Published in British journal of haematology (01.01.1997)
Published in British journal of haematology (01.01.1997)
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Ankyrin Napoli: a de novo deletional frameshift mutation in exon 16 of ankyrin gene (ANK1) associated with spherocytosis
del Giudice, E M, Hayette, S, Bozon, M, Perrotta, S, Alloisio, N, Vallier, A, Iolascon, A, Delaunay, J, Morlé, L
Published in British journal of haematology (01.06.1996)
Published in British journal of haematology (01.06.1996)
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Cytoskeletal behaviour in spectrin and in band 3 deficient spherocytic red cells: evidence for differentiated splenic conditioning role
Ingrosso, D, D'Angelo, S, Perrotta, S, d'Urzo, G, Iolascon, A, Perna, A F, Galletti, P, Zappia, V, Miraglia del Giudice, E
Published in British journal of haematology (01.04.1996)
Published in British journal of haematology (01.04.1996)
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Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele
Miraglia del Giudice, E, Francese, M, Polito, R, Nobili, B, Iolascon, A, Perrotta, S
Published in Haematologica (Roma) (01.05.1997)
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Published in Haematologica (Roma) (01.05.1997)
Journal Article
Mild elliptocytosis associated with the alpha 34 Arg-->Trp mutation in spectrin Genova (alpha I/74)
Perrotta, S, Miraglia del Giudice, E, Alloisio, N, Sciarratta, G, Pinto, L, Delaunay, J, Cutillo, S, Iolascon, A
Published in Blood (01.06.1994)
Published in Blood (01.06.1994)
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Spectrin cagliari. an Ala–>Gly substitution in helix 1 of beta spectrin repeat 17 that severely disrupts the structure and self-association of the erythrocyte spectrin heterodimer
Sahr, K.E., Coetzer, T.L., Moy, L.S., Derick, L.H., Chishti, A.H., Jarolim, P, Lorenzo, F, Miraglia del Giudice, E, Iolascon, A, Gallanello, R
Published in The Journal of biological chemistry (25.10.1993)
Published in The Journal of biological chemistry (25.10.1993)
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Spectrin Anastasia (alpha I/78): a new spectrin variant (alpha 45 Arg-->Thr) with moderate elliptocytogenic potential
Perrotta, S, Iolascon, A, De Angelis, F, Pagano, L, Colonna, G, Cutillo, S, Miraglia del Giudice, E
Published in British journal of haematology (01.04.1995)
Published in British journal of haematology (01.04.1995)
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A deletional frameshift mutation in spectrin beta-gene associated with hereditary elliptocytosis in spectrin Napoli
Wilmotte, R, Miraglia del Giudice, E, Marechal, J, Perrotta, S, de Mattia, D, Delaunay, J, Iolascon, A
Published in British journal of haematology (01.10.1994)
Published in British journal of haematology (01.10.1994)
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Molecular heterogeneity of hereditary elliptocytosis in Italy
Miraglia del Giudice, E, Perrotta, S, Sannino, E, De Angelis, F, Nobili, B, Iolascon, A
Published in Haematologica (Roma) (01.09.1994)
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Published in Haematologica (Roma) (01.09.1994)
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Rare frequencey of point mutations for codon 12, 13 and 61 of ras gene in italian neuroblastoma
Iolascon, A, Badiali, M, Pession, A, Basso, G, Losi, L, Delgiudice, E, Perrotta, S, Cutillo, S, Tonini, G
Published in International journal of oncology (01.09.1993)
Published in International journal of oncology (01.09.1993)
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A rapid method for the detection of alpha I/65 hereditary elliptocytosis
Iolascon, A, Miraglia del Giudice, E, Perrotta, S, Pinto, L, Cutillo, S
Published in Acta haematologica (1993)
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Published in Acta haematologica (1993)
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