Wolfram syndrome and WFS1 gene von Rigoli, L, Lombardo, F, Di Bella, C

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HER2 Status in Premalignant, Early, and Advanced Neoplastic Lesions of the Stomach von Caruso, R. A., Rigoli, L., Barresi, Valeria, Ieni, A., Tuccari, Giovanni

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Gene-Environment Interaction in Childhood Asthma von Rigoli, L, Briuglia, S, Caimmi, S, Ferraù, V, Gallizzi, R, Leonardi, S, La Rosa, M, Salpietro, C

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Phenotypical and genotypical expression of Wolfram syndrome in 12 patients from a Sicilian district where this syndrome might not be so infrequent as generally expected von Lombardo, F., Salzano, G., Di Bella, C., Aversa, T., Pugliatti, F., Cara, S., Valenzise, M., De Luca, F., Rigoli, L.

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TLR2 and TLR4 Gene Polymorphisms and Atopic Dermatitis in Italian Children: A Multicenter Study von Salpietro, C, Rigoli, L, Del Giudice, Miraglia M, Cuppari, C, Di Bella, C, Salpietro, A, Maiello, N, La Rosa, M, Marseglia, Gl, Leonardi, S, Briuglia, S, Ciprandi, G

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P1515: IMPACT OF GENOTYPE ON PANCREATIC IRON OVERLOAD AND IMPAIRED GLUCOSE METABOLISM IN THALASSEMIA MAJOR von Meloni, A., Pistoia, L., Santodirocco, M., Rigoli, L., Bosi, C., Pasin, F. M., Argento, C., Peritore, G., Fina, P., Positano, V., Cademartiri, F.

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TLR4 and NOD2/CARD15 Genetic Polymorphisms and their Possible Role in Gastric Carcinogenesis von RIGOLI, L, DI BELLA, C, CARUSO, R. A, FEDELE, F, PROCOPIO, V, AMORINI, M, LO GIUDICE, G, ROMEO, P, PUGLIATTI, F, FINOCCHIARO, G, LUCIANO, R

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Foveolar cells phagocytose apoptotic neutrophils in chronic active Helicobacter pylori gastritis von Caruso, R. A., Fedele, F., Di Bella, C., Mazzon, E., Rigoli, L.

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Molecular analysis of the CART gene in overweight and obese Italian children using family-based association methods von Rigoli, L, Munafò, C, Di Bella, C, Salpietro, A, Procopio, V, Salpietro, C

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Serum IL-23 in asthmatic children von Ciprandi, G, Cuppari, C, Salpietro, A, Tosca, M, Grasso, L, Rigoli, L, La Rosa, M, Marseglia, G L, Miraglia Del Giudice, M, Salpietro, C

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CO21 TWO NOVEL MITOCHONDRIAL DNA CONTROL REGION MUTATIONS IN CHILDREN WITH CYCLIC VOMITING SYNDROME von Fuoti, M, Martinazzi, S, Rigoli, L, Di Bella, C, Pugliatti, F, Salpietro, C, Romano, C, Ravelli, A

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Gastric adenomas: relationship between clinicopathological findings, Helicobacter pylori infection, APC mutations and COX-2 expression von Rocco, A., Caruso, R., Toracchio, S., Rigoli, L., Verginelli, F., Catalano, T., Neri, M., Curia, M.C., Ottini, L., Agnese, V., Bazan, V., Russo, A., Pantuso, G., Colucci, G., Mariani-Costantini, R., Nardone, G.

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Modifications of Nuclear Envelope in Tumour Cells of Human Gastric Carcinomas: An Ultrastructural Study von CARUSO, R. A, RIGOLI, L, VENUTI, A, FEDELE, F, PIZZI, G, QUATTROCCHI, E, FINOCCHIARO, G, LABATE, A, PAPARO, D, LUCIANO, R, PARISI, A

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Investigation of the eotaxin gene −426C→T, −384A→G and 67G→A single-nucleotide polymorphisms and atopic dermatitis in Italian children using family-based association methods... von Rigoli, L., Caminiti, L., Di Bella, C., Procopio, V., Cuppari, C., Vita, D., Barberio, G., Salpietro, C., Pajno, G. B.

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Morphological Evidence of Neutrophil-Tumor Cell Phagocytosis (Cannibalism) in Human Gastric Adenocarcinomas von Caruso, R. A., Muda, A. O., Bersiga, A., Rigoli, L., Inferrera, C.

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P6213Role of different phenotypic groups of thalassemia major patients studied by CMR von Pistoia, L, Meloni, A, Salvadori, S, Renne, S, Giuliano, P, Caccamo, P, Rocca, M, Rigoli, L, Smacchia, M P, Maffei, L, Spiga, A, Spadola, V, Romano, N, Maddaloni, D, Pepe, A

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NOD2/CARD15 and TLR4 single nucleotide polymorphisms (SNPs) in a cohort population with Inflammatory Bowel Disease from South of Italy: Survey of genotype–phenotype correlations von Rigoli, L, Romano, C, Fries, W, Procopio, V, Amorini, M, Lo Giudice, G, Salpietro, C

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Prognostic Value of Intratumoral Neutrophils in Advanced Gastric Carcinoma in a High-Risk Area in Northern Italy von Caruso, Rosario Alberto, Bellocco, Rino, Pagano, Marcello, Bertoli, Giovanni, Rigoli, Luciana, Inferrera, Cosimo

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Molecular analysis of sequence variants in the Fcε receptor Iβ gene and IL-4 gene promoter in Italian atopic families von RIGOLI, L, DI BELLA, C, PROCOPIO, V, BARBERIO, G, BARBERI, I, CAMINITI, L, LA GRUTTA, S, BRIUGLIA, S, SALPIETRO, C. D, PAJNO, G. B

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Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and/or deafness in an Italian family von Rigoli, L., Prisco, F., Caruso, R. A., Iafusco, D., Ursomanno, G., Zuccarello, D., Ingenito, N., Rigoli, M., Barberi, I.

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