Validation of a targeted gene panel sequencing for the diagnosis of hereditary chronic liver diseases von Ronzoni, Luisa, Marini, Ilaria, Passignani, Giulia, Malvestiti, Francesco, Marchelli, Daniele, Bianco, Cristiana, Pelusi, Serena, Prati, Daniele, Valenti, Luca

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Thalassemic erythrocytes release microparticles loaded with hemichromes by redox activation of p72Syk kinase von Ferru, Emanuela, Pantaleo, Antonella, Carta, Franco, Mannu, Franca, Khadjavi, Amina, Gallo, Valentina, Ronzoni, Luisa, Graziadei, Giovanna, Cappellini, Maria Domenica, Turrini, Francesco

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Preferences for prenatal tests for Down syndrome: an international comparison of the views of pregnant women and health professionals von Hill, Melissa, Johnson, Jo-Ann, Langlois, Sylvie, Lee, Hyun, Winsor, Stephanie, Dineley, Brigid, Horniachek, Marisa, Lalatta, Faustina, Ronzoni, Luisa, Barrett, Angela N, Advani, Henna V, Choolani, Mahesh, Rabinowitz, Ron, Pajkrt, Eva, van Schendel, Rachèl V, Henneman, Lidewij, Rommers, Wieke, Bilardo, Caterina M, Rendeiro, Paula, Ribeiro, Maria João, Rocha, José, Bay Lund, Ida Charlotte, Petersen, Olav B, Becher, Naja, Vogel, Ida, Stefánsdottir, Vigdis, Ingvarsdottir, Sigrun, Gottfredsdottir, Helga, Morris, Stephen, Chitty, Lyn S

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Interstitial 6q25 microdeletion syndrome: ARID1B is the key gene von Ronzoni, Luisa, Tagliaferri, Francesco, Tucci, Arianna, Baccarin, Marco, Esposito, Susanna, Milani, Donatella

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Genetics: A new clinical tool for the hepatologist von Valenti, Luca, Ronzoni, Luisa

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Clinical and genetic determinants of the fatty liver–coagulation balance interplay in individuals with metabolic dysfunction von Valenti, Luca, Tripodi, Armando, La Mura, Vincenzo, Pelusi, Serena, Bianco, Cristiana, Scalambrino, Erica, Margarita, Sara, Malvestiti, Francesco, Ronzoni, Luisa, Clerici, Marigrazia, D’Ambrosio, Roberta, Fraquelli, Mirella, Carpani, Rossana, Prati, Daniele, Peyvandi, Flora

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Ultrasound 2-D and 3-D diagnosis of Rubinstein–Taybi syndrome in a 21-week-old fetus von D’Ambrosi, Francesco, Ronzoni, Luisa, Villa, Roberta, De Marinis, Stefano, Cetera, Giulia Emily, Soldavini, Chiara Maria, Ferrazzi, Enrico

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Oxidative stress modulates heme synthesis and induces peroxiredoxin-2 as a novel cytoprotective response in β-thalassemic erythropoiesis von DE FRANCESCHI, Lucia, BERTOLDI, Mariarita, DE FALCO, Luigia, FRANCO, Sara Santos, RONZONI, Luisa, TURRINI, Franco, COLANCECCO, Alessandra, CAMASCHELLA, Clara, CAPPELLINI, Maria Domenica, IOLASCON, Achille

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Circulating indian hedgehog is a marker of the hepatocyte-TAZ pathway in experimental NASH and is elevated in humans with NASH von Moore, Mary Patricia, Wang, Xiaobo, Shi, Hongxue, Meroni, Marica, Cherubini, Alessandro, Ronzoni, Luisa, Parks, Elizabeth J., Ibdah, Jamal A., Rector, R. Scott, Valenti, Luca, Dongiovanni, Paola, Tabas, Ira

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SARS-CoV-2 infection in children: A 24 months experience with focus on risk factors in a pediatric tertiary care hospital in Milan, Italy von Di Pietro, Giada Maria, Ronzoni, Luisa, Meschia, Lorenzo Maria, Tagliabue, Claudia, Lombardi, Angela, Pinzani, Raffaella, Bosis, Samantha, Marchisio, Paola Giovanna, Valenti, Luca

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ABCC2 p.R393W variant contributes to Dubin-Johnson syndrome by targeting MRP2 to proteasome degradation von Sun, Rong-Yue, Chen, Yi-Ming, Zhu, Mian-Mian, Sun, Ji-an, Wang, Hong-Wei, Wu, Chen-Yu, Zhu, Ting, Gong, Yu-Jing, Lu, Chao-Sheng, Ronzoni, Luisa, Valenti, Luca, Zheng, Ming-Hua, Wang, Dan

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Response to "characteristics of 2p15-p16.1 microdeletion syndrome: review and description of two additional patients" von Ronzoni, Luisa, Saletti, Veronica, Scuvera, Giulietta, Esposito, Susanna, Milani, Donatella

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Selective toxicity of dihydroartemisinin on human CD34+ erythroid cell differentiation von Finaurini, Sara, Ronzoni, Luisa, Colancecco, Alessandra, Cattaneo, Alessandra, Cappellini, Maria Domenica, Ward, Stephen A, Taramelli, Donatella

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Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins: A genotype-phenotype analysis von Ronzoni, Luisa, Peron, Angela, Bianchi, Vera, Baccarin, Marco, Guerneri, Silvana, Silipigni, Rosamaria, Lalatta, Faustina, Bedeschi, Maria Francesca

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Erythroid differentiation and maturation from peripheral CD34 + cells in liquid culture: Cellular and molecular characterization von Ronzoni, Luisa, Bonara, Paola, Rusconi, Daniela, Frugoni, Cecilia, Libani, Ilaria, Cappellini, Maria Domenica

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Front Cover von Shalaby, Sarah, Ronzoni, Luisa, Hernandez‐Gea, Virginia, Valenti, Luca

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EPO receptor gain-of-function causes hereditary polycythemia, alters CD34 cell differentiation and increases circulating endothelial precursors von Perrotta, Silverio, Cucciolla, Valeria, Ferraro, Marcella, Ronzoni, Luisa, Tramontano, Annunziata, Rossi, Francesca, Scudieri, Anna Chiara, Borriello, Adriana, Roberti, Domenico, Nobili, Bruno, Cappellini, Maria Domenica, Oliva, Adriana, Amendola, Giovanni, Migliaccio, Anna Rita, Mancuso, Patrizia, Martin-Padura, Ines, Bertolini, Francesco, Yoon, Donghoon, Prchal, Josef T, Della Ragione, Fulvio

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Congenital dyserythropoietic anemia type II: molecular analysis and expression of the SEC23B gene von Punzo, Francesca, Bertoli-Avella, Aida M, Scianguetta, Saverio, Della Ragione, Fulvio, Casale, Maddalena, Ronzoni, Luisa, Cappellini, Maria D, Forni, Gianluca, Oostra, Ben A, Perrotta, Silverio

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Rare ATG7 genetic variants predispose patients to severe fatty liver disease von Baselli, Guido A., Jamialahmadi, Oveis, Pelusi, Serena, Ciociola, Ester, Malvestiti, Francesco, Saracino, Marco, Santoro, Luigi, Cherubini, Alessandro, Dongiovanni, Paola, Maggioni, Marco, Bianco, Cristiana, Tavaglione, Federica, Cespiati, Annalisa, Mancina, Rosellina M., D’Ambrosio, Roberta, Vaira, Valentina, Petta, Salvatore, Miele, Luca, Vespasiani-Gentilucci, Umberto, Federico, Alessandro, Pihlajamaki, Jussi, Bugianesi, Elisabetta, Fracanzani, Anna L., Reeves, Helen L., Soardo, Giorgio, Prati, Daniele, Romeo, Stefano, Valenti, Luca VC, Borroni, Vittorio, Liguori, Antonio, Ronzoni, Luisa, Cherubini, Alessandro, Santoro, Luigi, Tomasi, Melissa, Lombardi, Angela, Ostadreza, Mahnoosh, Casirati, Elia, Marini, Ilaria, Maier, Silvia, Rosso, Chiara, Baroni, Gianluca Svegliati, Santaniello, Carlo, Dallio, Marcello

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The genetics of portal hypertension: Recent developments and the road ahead von Shalaby, Sarah, Ronzoni, Luisa, Hernandez‐Gea, Virginia, Valenti, Luca

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