Pontocerebellar hypoplasia: Clinical, pathologic, and genetic studies von CASSANDRINI, D, BIANCHERI, R, EMMA, F, MEZZANO, P, POLITI, M. R, LAVERDA, A. M, ZARA, F, PAVONE, L, SIMONATI, A, LEUZZI, V, SANTORELLI, F. M, BERTINI, E, TESSA, A, DI ROCCO, M, DI CAPUA, M, BRUNO, C, DENORA, P. S, SARTORI, S, ROSSI, A, NOZZA, P

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Ligurian experience on neonatal hearing screening: clinical and epidemiological aspects von Calevo, MG, Mezzano, P, Zullino, E, Padovani, P, Serra, G

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A randomised control study comparing the Infant Flow Driver with nasal continuous positive airway pressure in preterm infants von Mazzella, M, Bellini, C, Calevo, M G, Campone, F, Massocco, D, Mezzano, P, Zullino, E, Scopesi, F, Arioni, C, Bonacci, W, Serra, G

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Neonatal hearing screening model: An Italian regional experience von Calevo, M. G., Mezzano, P., Zullino, E., Padovani, P., Scopesi, F., Serra, G., The Stern Group

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Cerebral ultrasound images in prenatal cytomegalovirus infection von TOMA, P, MAGNANO, G. M, MEZZANO, P, LAZZINI, F, BONACCI, W, SERRA, G

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De novo (15;21) unbalanced translocation of paternal origin in a girl with prader-willi syndrome von Cuoco, C., Bicocchi, M. P., Granata, D., Mezzano, P., Serra, G.

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The "candlestick sign" on cerebral ultrasound von Tomà, P, Mezzano, P, Serra, G

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Podocyte-specific overexpression of wild type or mutant trpc6 in mice is sufficient to cause glomerular disease von Krall, Paola, Canales, Cesar P, Kairath, Pamela, Carmona-Mora, Paulina, Molina, Jessica, Carpio, J Daniel, Ruiz, Phillip, Mezzano, Sergio A, Li, Jing, Wei, Changli, Reiser, Jochen, Young, Juan I, Walz, Katherina

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Global burden of disease: acute-on-chronic liver failure, a systematic review and meta-analysis von Mezzano, Gabriel, Juanola, Adria, Cardenas, Andres, Mezey, Esteban, Hamilton, James P, Pose, Elisa, Graupera, Isabel, Ginès, Pere, Solà, Elsa, Hernaez, Ruben

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Diagnosis of suspected inherited platelet function disorders: results of a worldwide survey von Gresele, P., Harrison, P., Bury, L., Falcinelli, E., Gachet, C., Hayward, C. P., Kenny, D., Mezzano, D., Mumford, A. D., Nugent, D., Nurden, A. T., Orsini, S., Cattaneo, M.

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Diagnosis of inherited platelet function disorders: guidance from the SSC of the ISTH von Gresele, P., Harrison, P., Gachet, C., Hayward, C., Kenny, D., Mezzano, D., Mumford, A. D., Nugent, D., Nurden, A. T., Cattaneo, M.

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Inhibition of platelet activation and thrombus formation by adenosine and inosine: studies on their relative contribution and molecular modeling von Fuentes, Eduardo, Pereira, Jaime, Mezzano, Diego, Alarcón, Marcelo, Caballero, Julio, Palomo, Iván

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Immobilized fibrinogen activates human platelets through glycoprotein VI von Mangin, Pierre H, Onselaer, Marie-Blanche, Receveur, Nicolas, Le Lay, Nicolas, Hardy, Alexander T, Wilson, Clare, Sanchez, Ximena, Loyau, Stéphane, Dupuis, Arnaud, Babar, Amir K, Miller, Jeanette Lc, Philippou, Helen, Hughes, Craig E, Herr, Andrew B, Ariëns, Robert As, Mezzano, Diego, Jandrot-Perrus, Martine, Gachet, Christian, Watson, Steve P

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Laboratory monitoring of P2Y12 inhibitors: communication from the SSC of the ISTH von Frelinger, A. L., Gachet, C., Mumford, A. D., Noris, P., Mezzano, D., Harrison, P., Gresele, P.

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High prevalence of bleeders of unknown cause among patients with inherited mucocutaneous bleeding. A prospective study of 280 patients and 299 controls von Quiroga, Teresa, Goycoolea, Manuela, Panes, Olga, Aranda, Eduardo, Martinez, Carlos, Belmont, Sabine, Munoz, Blanca, Zuniga, Pamela, Pereira, Jaime, Mezzano, Diego

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An adenine insertion in exon 6 of human GP6 generates a truncated protein associated with a bleeding disorder in four Chilean families von Matus, V., Valenzuela, G., Sáez, C. G., Hidalgo, P., Lagos, M., Aranda, E., Panes, O., Pereira, J., Pillois, X., Nurden, A. T., Mezzano, D.

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The MEST score provides earlier risk prediction in lgA nephropathy von Barbour, Sean J., Espino-Hernandez, Gabriela, Herzenberg, Andrew M., Cook, T., Troyanov, S., Alpers, C., Berthoux, F., Bonsib, S., D’Agati, V., Emancipator, S., Florquin, S., Groene, H., Hill, P., Hogg, R., Hsu, S., Hunley, T., Jennette, C., Joh, K., Julian, B., Leung, C., Liu, Z., Massat, A., Mackinnon, B., Walker, P., Weening, J., Yoshikawa, N., Zhang, H., Cattran, D.C., Feehally, J., Maixnerova, D., Lundberg, S., Fuiano, L., Beltrame, G., Rollino, C., Camilla, R., Peruzzi, L., Praga, M., Polci, R., Segoloni, G., Colla, L., Pani, A., Angioi, A., Piras, L., JF, Cancarini, G., Ravera, S., Durlik, M., Moggia, E., Pugliese, F., Caliskan, Y., Sever, M., Locatelli, F., Del Vecchio, L., Wetzels, J.F.M., Berg, U., Ots-Rosenberg, M., Topaloglu, R., D’Amico, M., Stangou, M., Giacchino, F., Goumenos, D., Siamopoulos, K., Galliani, M., Quaglia, M., Salvadori, M., Cirami, L., Kloster Smerud, H., Stellato, T., Egido, J., Martin, C., Floege, J., Eitner, F., Bernich, P., Menè, P., Morosetti, M., van Kooten, C., Rabelink, T., Reinders, M.E.J., Boria Grinyo, J.M., Cusinato, S., Savoldi, S., Mizerska-Wasiak, M., Martina, G., Migotto, C., Triolo, G., Mariano, F., Boero, R., Giannakakis, C., Honsova, E., Sundelin, B., Di Palma, A.M., Asunis, A.M., Tardanico, R., Perkowska-Ptasinska, A., Pantzaki, A., Riispere, Z., Casartelli, D., Cannata Ortiz, P., Bajema, I., Ioachim, E.

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Quantitative impact of using different criteria for the laboratory diagnosis of type 1 von Willebrand disease von Quiroga, T., Goycoolea, M., Belmont, S., Panes, O., Aranda, E., Zúñiga, P., Pereira, J., Mezzano, D.

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Reply to: “Acute-on-chronic liver failure in East-Asia: an underestimated issue with limited data” von Juanola, Adrià, Mezzano, Gabriel, Hamilton, James P, Ginès, Pere, Solà, Elsa, Hernaez, Ruben

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Serotonin- and Dopamine-Related Gene Expression in db/db Mice Islets and in MIN6 β-Cells Treated with Palmitate and Oleate von Santos, J. L., Cortés, V. A., Diego, Mezzano, Valenzuela, R., Galgani, J. E., Olmos, P., Busso, Dolores, Mizgier, M. L., Cataldo, L. R., Aranda, E.

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