Citizens and family doctors facing awareness and management of traditional cardiovascular risk factors: Results from the Global Cardiovascular Risk Reduction Project (Help Your Hea... by Celentano, A., Panico, S., Palmieri, V., Guillaro, B., Brancati, C., Palma Esposito, N.Di, Arezzi, E., Setola, C., Piccinocchi, G., Canfora, G., Rubba, P., Minno, G.Di, Mancini, M.

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Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single-strand conformation and sequence analysis by CALABRO, V, MASON, P. J, FILOSA, S, CIVITELLI, D, CITTADELLA, R, TAGARELLI, A, MARTINI, G, BRANCATI, C, LUZZATTO, L

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Severe erythrocyte adenylate kinase deficiency due to homozygous A → G substitution at codon 164 of human AK1 gene associated with chronic haemolytic anaemia by Qualtieri, A., Pedace, V., Bisconte, M. G., Bria, M., Gulino, B., Andreoli, V., Brancati, C.

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Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency in south-east Sicily by CITTADELLA, R., CIVITELLI, D., MANNA, I., AZZIA, N., DI CATALDO, A., SCHILIROA, G., BRANCATI, C.

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Spectrin Cosenza: a novel β chain variant associated with Sp αI/74 hereditary elliptocytosis by Qualtieri, A., Pasqua, A., Bisconte, M. G., Le Pera, M., Brancati, C.

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Genetic Polymorphism of the α-Globin Haplotypes in a Population from Calabria (Southern Italy) by Modiano, G., Brancati, C., Marinucci, M., Massa, A., Mavilio, F., Tentori, L.

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Delineation of the molecular basis of δ- and normal HbA2 β-thalassemia by MOI, P, PAGLIETTI, E, SANNA, A, BRANCATI, C, TAGARELLI, A, GALANELLO, R, CAO, A, PIRASTU, M

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DYS19, D12S67, and D1S80 Polymorphisms in Population Samples from Southern Italy and Greece by FALCONE, E., SPADAFORA, P., DE LUCA, M., RUFFOLO, R., BRANCATI, C., DE BENEDICTIS, G.

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A Simple and Rapid Nonisotopic Method for Sizing CAG Repeats in the SCA1 Gene by Annesi, G., Muglia, M., Conforti, F.L., Leone, O., Grandinetti, C., Imbrogno, E., Gabriele, A.L., Naso, F., Brancati, C.

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Analysis of the (CAG)n Repeat at the IT15 Locus in a Population from Calabria (Southern Italy) by LEONE, O., MUGLIA, M., GABRIELE, A.L., ANNESI, G., CONFORTI, F.L., IMBROGNO, E., IMBROGNO, L., BRANCATI, C.

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RFLPs of the APOB Gene: Comparative Study between Greeks and Southern Italian Peoples by DE BENEDICTIS, G., LEONE, O., FALCONE, E., ROSE, G., BRANCATI, C., CAROTENUTO, L.

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HB Valletta [β87(F3)THR →PRO] DUE to an A→C Substitution at Codon 87 in a Calabrian Family with α-Thalassemia by Qualtieri, A., Andreoli, V., Crescibene, L., De Marco, E. V., Muglia, M., Gabriele, A. L., Annesi, G., Brancati, C.

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Follow-up study of thyroid function in polytransfused thalassemic patients by Maggiolini, M, De Luca, G, Bria, M, Sisci, D, Aquila, S, Pezzi, V, Lanzino, M, Giorno, A, Tamburrini, O, Della Sala, M, Corcioni, E, Brancati, C, Ando, S

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Molecular basis for HbH disease in Italy: geographical distribution of deletional and nondeletional alpha-thalassemia haplotypes by Di Rienzo, A, Novelletto, A, Aliquò, M C, Bianco, I, Tagarelli, A, Brancati, C, Colombo, B, Felicetti, L

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Delta +-thalassemia in Sardinia by Pirastu, M, Galanello, R, Melis, MA, Brancati, C, Tagarelli, A, Cao, A, Kan, YW

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Homozygous βδ Thalassaemia (βδ Microcythaemia) by BRANCATI, C, BAGLIONI, C

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Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency in south-east Sicily by CITTADELLA, R., CIVITELLI, D., MANNA, I., AZZIA, N., DI CATALDO, A., SCHILIROA, G., BRANCATI, C.

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G1m(1) and G1m(2) Allotypes in Albanian Towns of Calabria by De Benedictis, G., Rosea, G., Brancati, C., Tagarelli, A.

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Hb MOLFETTA [β126(H4)Val→Leu, GTG→CTG]: A NEW, SILENT, NEUTRAL β CHAIN VARIANT FOUND IN AN ITALIAN WOMAN by Qualtieri, Antonio, Le Pera, Maria, Pedace, Vera, Magariello, Angela, Brancati, Carlo

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Severe erythrocyte adenylate kinase deficiency due to homozygous A arrow right G substitution at codon 164 of human AK1 gene associated with chronic haemolytic anaemia by Qualtieri, A, Pedace, V, Bisconte, M G, Bria, M, Gulino, B, Andreoli, V, Brancati, C

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