Gene expression analysis in calcific tendinopathy of the rotator cuff von Oliva, F, Barisani, D, Grasso, A, Maffulli, N

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Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-κB signalling von Trynka, G, Zhernakova, A, Romanos, J, Franke, L, Hunt, K A, Turner, G, Bruinenberg, M, Heap, G A, Platteel, M, Ryan, A W, de Kovel, C, Holmes, G K T, Howdle, P D, Walters, J R F, Sanders, D S, Mulder, C J J, Mearin, M L, Verbeek, W H M, Trimble, V, Stevens, F M, Kelleher, D, Barisani, D, Bardella, M T, McManus, R, van Heel, D A, Wijmenga, C

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Six new coeliac disease loci replicated in an Italian population confirm association with coeliac disease von Romanos, J, Barisani, D, Trynka, G, Zhernakova, A, Bardella, M T, Wijmenga, C

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Wheat amylase trypsin inhibitors drive intestinal inflammation via activation of toll-like receptor 4 von Junker, Yvonne, Zeissig, Sebastian, Kim, Seong-Jun, Barisani, Donatella, Wieser, Herbert, Leffler, Daniel A, Zevallos, Victor, Libermann, Towia A, Dillon, Simon, Freitag, Tobias L, Kelly, Ciaran P, Schuppan, Detlef

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Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variants von Romanos, Jihane, Rosén, Anna, Kumar, Vinod, Trynka, Gosia, Franke, Lude, Szperl, Agata, Gutierrez-Achury, Javier, van Diemen, Cleo C, Kanninga, Roan, Jankipersadsing, Soesma A, Steck, Andrea, Eisenbarth, Georges, van Heel, David A, Cukrowska, Bozena, Bruno, Valentina, Mazzilli, Maria Cristina, Núñez, Concepcion, Bilbao, Jose Ramon, Mearin, M Luisa, Barisani, Donatella, Rewers, Marian, Norris, Jill M, Ivarsson, Anneli, Boezen, H Marieke, Liu, Edwin, Wijmenga, Cisca

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F.N.38 HEPCIDIN EXPRESSION AT HEPATIC, SERUM AND URINARY LEVEL IN SUBJECTS WITH DIFFERENT IRON PHENOTYPES von Pozzi, M, Pelucchi, S, Trombini, P, Mariani, R, Coletti, S, Vanessi, S, Nemeth, E, Tomosugi, N, Barisani, D, Piperno, A

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Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF- B signalling von Trynka, G., Zhernakova, A., Romanos, J., Franke, L., Hunt, K. A., Turner, G., Bruinenberg, M., Heap, G. A., Platteel, M., Ryan, A. W., de Kovel, C., Holmes, G. K. T., Howdle, P. D., Walters, J. R. F., Sanders, D. S., Mulder, C. J. J., Mearin, M. L., Verbeek, W. H. M., Trimble, V., Stevens, F. M., Kelleher, D., Barisani, D., Bardella, M. T., McManus, R., van Heel, D. A., Wijmenga, C.

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A major histocompatibility complex class I-related Fc receptor for IgG on rat hepatocytes von Blumberg, R S, Koss, T, Story, C M, Barisani, D, Polischuk, J, Lipin, A, Pablo, L, Green, R, Simister, N E

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Intravesical prostaglandin e2 effectiveness in the prevention of urinary retention after transvaginal reconstruction of the pubo-cervical fascia and short arm sling according to La... von QUADRI, G., NATALE, N., SPREAFICO, C., BELLONI, C., BARISANI, D., LAHODNY, J.

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OC3.05.8 TRANSGLUTAMINASE EXPRESSION IN THE HEPATOBILIARY TRACT von Roncoroni, L, Elli, L, Dogliotti, E, Barisani, D, Doneda, L, Marchelli, D, Terranegra, A, Fregoni, F, Piodi, L, Bardella, M.T

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Genomic organization and transcription of the human retinol dehydrogenase 10 (RDH10) gene von Picozzi, P., Marozzi, A., Fornasari, D., Benfante, R., Barisani, D., Meneveri, R., Ginelli, E.

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TrkA pathway activation induced by amyloid-beta (Abeta) von Bulbarelli, Alessandra, Lonati, Elena, Cazzaniga, Emanuela, Re, Francesca, Sesana, Silvia, Barisani, Donatella, Sancini, Giulio, Mutoh, Tatsuro, Masserini, Massimo

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Expression of hepcidin and other iron-related genes in type 3 hemochromatosis due to a novel mutation in transferrin receptor-2 von Pelucchi, Sara, Mariani, Raffaella, Trombini, Paola, Coletti, Sabina, Pozzi, Matteo, Paolini, Valentina, Barisani, Donatella, Piperno, Alberto

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Mutation analysis and HFE sequencing of two families with iron overload von Barisani, D

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Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy von Combi, Romina, Grioni, Daniele, Contri, Margherita, Redaelli, Serena, Redaelli, Francesca, Bassi, Maria Teresa, Barisani, Donatella, Lavitrano, Maria Luisa, Tredici, Giovanni, Tenchini, Maria Luisa, Bertolini, Mario, Dalprà, Leda

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Genetic Risk Model for Celiac Disease Helps Identify High-risk Individuals von van Diemen, C, Romanos, J, Nolte, I, Barisani, D, McManus, R, van Heel, D, Wijmenga, C

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IL-10 polymorphisms are associated with early-onset celiac disease and severe mucosal damage in patients of Caucasian origin von Barisani, Donatella, Ceroni, Stefano, Meneveri, Raffaella, Cesana, Bruno M, Bardella, Maria Teresa

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Transferrin Receptor 1 (TfR1) and Putative Stimulator of Fe Transport (SFT) Expression in Iron Deficiency and Overload: An Overview von Barisani, Donatella, Conte, Dario

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Adaptive changes of duodenal iron transport proteins in celiac disease von Barisani, Donatella, Parafioriti, Antonina, Bardella, Maria Teresa, Zoller, Heinz, Conte, Dario, Armiraglio, Elisabetta, Trovato, Cristina, Koch, Robert O, Weiss, Gunter

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Hemochromatosis gene mutations and iron metabolism in celiac disease von Barisani, D, Ceroni, S, Del Bianco, S, Meneveri, R, Bardella, MT

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