The impact of ICT on the work patterns of managers and their organisations by Birchall, David W, Giambona, G

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An evaluation-led virtual action learning programme - was the theory put into practice? by Giambona, G., Birchall, D.W.

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Celocentesis for early prenatal diagnosis of hemoglobinopathy by Makrydimas, G., Damiani, G., Jakil, C., Cigna, V., Orlandi, M., Picciotto, F., Schillaci, G., Cassarà, F., Vinciguerra, M., Leto, F., Giambona, A., Maggio, A., Nicolaides, K. H.

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Reply by Makrydimas, G., Damiani, G., Jakil, C., Cigna, V., Orlandi, M., Picciotto, F., Schillaci, G., Cassarà, F., Vinciguerra, M., Leto, F., Giambona, A., Maggio, A., Nicolaides, K. H.

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Reply by Makrydimas, G, Damiani, G, Jakil, C, Cigna, V, Orlandi, M, Picciotto, F, Schillaci, G, Cassarà, F, Vinciguerra, M, Leto, F, Giambona, A, Maggio, A, Nicolaides, K H

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Reply by Makrydimas, G., Damiani, G., Jakil, C., Cigna, V., Orlandi, M., Picciotto, F., Schillaci, G., Cassarà, F., Vinciguerra, M., Leto, F., Giambona, A., Maggio, A., Nicolaides, K. H.

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Coheredity of a new silent mutation: c.‐29G>T, with a severe β‐thal mutation in a patient with β‐thalassemia intermediate by Vinciguerra, M., Passarello, C., Cassarà, F., Leto, F., Cannata, M., Calvaruso, G., Renda, D., Maggio, A., Giambona, A.

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Co-heredity of silent CAP + 1570 T>C (HBB:c96T>C) defect and severe β-thal mutation: a cause of mild β-thalassemia intermedia by Vinciguerra, M., Passarello, C., Cassarà, F., Leto, F., Cannata, M., Calvaruso, G., Di Maggio, R., Renda, D., Maggio, A., Giambona, A.

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Reply by Makrydimas, G, Damiani, G, Jakil, C, Cigna, V, Orlandi, M, Picciotto, F, Schillaci, G, Cassarà, F, Vinciguerra, M, Leto, F, Giambona, A, Maggio, A, Nicolaides, K H

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Analysis of delta-globin gene alleles in the Sicilian population: identification of five new mutations by Giambona, A, Passarello, C, Ruggeri, G, Renda, D, Teresi, P, Anza, M, Maggio, A

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Evaluation of the adequacy of levothyroxine replacement therapy in patients with central hypothyroidism by FERRETTI, E, PERSANI, L, JAFFRAIN-REA, M.-L, GIAMBONA, S, TAMBURRANO, G, BECK-PECCOZ, P

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Significance of borderline hemoglobin A2 values in an Italian population with a high prevalence of {beta}-thalassemia by Giambona, Antonino, Passarello, Cristina, Vinciguerra, Margherita, Muli, Rita Li, Teresi, Pietro, Anza, Maurizio, Ruggeri, Gaetano, Renda, Disma, Maggio, Aurelio

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Attitude of potential users in Sicily towards preimplantation genetic diagnosis for beta-thalassaemia and aneuploidies by Chamayou, S, Guglielmino, A, Giambona, A, Siciliano, S, Di Stefano, G, Scibilia, G, Humeau, C, Maggio, A, Di Leo, S

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Body composition analysis by dual energy x-ray absorptiometry and anthropometry in adults with childhood-onset growth hormone (GH) deficiency before and after six months of recombi... by SARTORIO, A, NARICI, M, CONTI, A, GIAMBONA, S, ORTOLANI, S, FAGLIA, G

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P-4. PGD for β-thalassaemia in Sicily by Giambona, A, D'Alcamo, E, Siciliano, S, Leto, F, Gullo, D, Benigno, M, Ruvolo, G, Manno, M, Cefalu, E, Guastella, G, Cittadini, E, Maggio, A

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αααanti-4.2 Haplotype and heterozygous β° thalassemia in a Sicilian family by Acuto, S., Butticè, G., Saitta, B., Pirrone, A. M., Gambino, R., Costa, C., Giambona, A., Lo Gioco, P., Di Marzo, R., Maggio, A.

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αααanti-4.2haplotype and heterozygous β° thalassemia in a sicilian family by ACUTO, S, BUTTICE, G, SAITTA, B, PIRRONE, A. M, GAMBINO, R, COSTA, C, GIAMBONA, A, LO GIOCO, P, DI MARZO, R, MAGGIO, A

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alpha alpha alpha anti-4.2 Haplotype and heterozygous beta null thalassemia in a Sicilian family by Acuto, S, Butticé, G, Saitta, B, Pirrone, A M, Gambino, R, Costa, C, Giambona, A, Lo Gioco, P, Di Marzo, R, Maggio, A

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