Political alignments and distributive politics at the municipal level in federal countries von Moscovich, Lorena, Brusco, Valeria

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Hacia una agenda de indagación sobre nuevos comportamientos electorales: percepciones e interpretaciones sobre política, derechos y retrocesos de mujeres trabajadoras del sector in... von Brusco, Valeria

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Derecha radical y subjetividad política en la Argentina. Qué hay detrás del voto a Javier Milei von Nazareno, Marcelo, Brusco, Valeria

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Vote Buying in Argentina von Brusco, Valeria, Nazareno, Marcelo, Stokes, Susan C.

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Reditos Y Peligros Electorales Del Gasto Publico En La Argentina von Nazareno, Marcelo, Stokes, Susan, Brusco, Valeria

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Reditos Y Peligros Electorales Del Gasto Publico En La Argentina von Nazareno, Marcelo, Stokes, Susan, Brusco, Valeria

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Interest and electoral risks in Argentine public spending von Nazareno, Marcelo, Stokes, Susan, Brusco, Valeria

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EphA2 Expression in Bone Sarcomas: Bioinformatic Analyses and Preclinical Characterization in Patient-Derived Models of Osteosarcoma, Ewing's Sarcoma and Chondrosarcoma von Giordano, Giorgia, Merlini, Alessandra, Ferrero, Giulio, Mesiano, Giulia, Fiorino, Erika, Brusco, Silvia, Centomo, Maria Laura, Leuci, Valeria, D'Ambrosio, Lorenzo, Aglietta, Massimo, Sangiolo, Dario, Grignani, Giovanni, Pignochino, Ymera

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Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans von Gofin, Yoel, Mackay, Laura Palmer, Machol, Keren, Keswani, Sundeep, Potocki, Lorraine, Di Gregorio, Eleonora, Naretto, Valeria, Brusco, Alfredo, Hernandez-Garcia, Andres, Scott, Daryl

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eP127 - Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans von Gofin, Yoel, Mackay, Laura Palmer, Machol, Keren, Keswani, Sundeep, Potocki, Lorraine, Di Gregorio, Eleonora, Naretto, Valeria, Brusco, Alfredo, Hernandez-Garcia, Andres, Scott, Daryl

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Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans von Gofin, Yoel, Mackay, Laura Palmer, Machol, Keren, Keswani, Sundeep, Potocki, Lorraine, Di Gregorio, Eleonora, Naretto, Valeria Giorgia, Brusco, Alfredo, Hernandez‐Garcia, Andres, Scott, Daryl A.

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BRAT1-related disorders: phenotypic spectrum and phenotype-genotype correlations from 97 patients von Engel, Camille, Valence, Stéphanie, Delplancq, Geoffroy, Maroofian, Reza, Accogli, Andrea, Agolini, Emanuele, Alkuraya, Fowzan S, Baglioni, Valentina, Bagnasco, Irene, Becmeur-Lefebvre, Mathilde, Bertini, Enrico, Borggraefe, Ingo, Brischoux-Boucher, Elise, Bruel, Ange-Line, Brusco, Alfredo, Bubshait, Dalal K, Cabrol, Christelle, Cilio, Maria Roberta, Cornet, Marie-Coralie, Coubes, Christine, Danhaive, Olivier, Delague, Valérie, Denommé-Pichon, Anne-Sophie, Di Giacomo, Marilena Carmela, Doco-Fenzy, Martine, Engels, Hartmut, Cremer, Kirsten, Gérard, Marion, Gleeson, Joseph G, Heron, Delphine, Goffeney, Joanna, Guimier, Anne, Harms, Frederike L, Houlden, Henry, Iacomino, Michele, Kaiyrzhanov, Rauan, Kamien, Benjamin, Karimiani, Ehsan Ghayoor, Kraus, Dror, Kuentz, Paul, Kutsche, Kerstin, Lederer, Damien, Massingham, Lauren, Mignot, Cyril, Morris-Rosendahl, Déborah, Nagarajan, Lakshmi, Odent, Sylvie, Ormières, Clothilde, Partlow, Jennifer Neil, Pasquier, Laurent, Penney, Lynette, Philippe, Christophe, Piccolo, Gianluca, Poulton, Cathryn, Putoux, Audrey, Rio, Marlène, Rougeot, Christelle, Salpietro, Vincenzo, Scheffer, Ingrid, Schneider, Amy, Srivastava, Siddharth, Straussberg, Rachel, Striano, Pasquale, Valente, Enza Maria, Venot, Perrine, Villard, Laurent, Vitobello, Antonio, Wagner, Johanna, Wagner, Matias, Zaki, Maha S, Zara, Federizo, Lesca, Gaetan, Yassaee, Vahid Reza, Miryounesi, Mohammad, Hashemi-Gorji, Farzad, Beiraghi, Mehran, Ashrafzadeh, Farah, Galehdari, Hamid, Walsh, Christopher, Novelli, Antonio, Tacke, Moritz, Sadykova, Dinara, Maidyrov, Yerdan, Koneev, Kairgali, Shashkin, Chingiz, Capra, Valeria, Zamani, Mina, Van Maldergem, Lionel, Burglen, Lydie, Piard, Juliette

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Microduplications of ARID1A and ARID1B cause a novel clinical and epigenetic distinct BAFopathy von van der Sluijs, Pleuntje J., Moutton, Sébastien, Dingemans, Alexander J.M., Weis, Denisa, Levy, Michael A., Boycott, Kym M., Arberas, Claudia, Baldassarri, Margherita, Beneteau, Claire, Brusco, Alfredo, Coutton, Charles, Dabir, Tabib, Dentici, Maria L., Devriendt, Koenraad, Faivre, Laurence, van Haelst, Mieke M., Jizi, Khadije, Kempers, Marlies J., Kerkhof, Jennifer, Kharbanda, Mira, Lachlan, Katherine, Marle, Nathalie, McConkey, Haley, Mencarelli, Maria A., Mowat, David, Niceta, Marcello, Nicolas, Claire, Novelli, Antonio, Orlando, Valeria, Pichon, Olivier, Rankin, Julia, Relator, Raissa, Ropers, Fabienne G., Rosenfeld, Jill A., Sachdev, Rani, Sandaradura, Sarah A., Shukarova-Angelovska, Elena, Steenbeek, Duco, Tartaglia, Marco, Tedder, Matthew A., Trajkova, Slavica, Winer, Norbert, Woods, Jeremy, de Vries, Bert B.A., Sadikovic, Bekim, Alders, Marielle, Santen, Gijs W.E.

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Congenital Sensorineural Hearing Loss and Inborn Pigmentary Disorders: First Report of Multilocus Syndrome in Piebaldism von Gironi, Laura Cristina, Colombo, Enrico, Brusco, Alfredo, Grosso, Enrico, Naretto, Valeria Giorgia, Guala, Andrea, Di Gregorio, Eleonora, Zonta, Andrea, Zottarelli, Francesca, Pasini, Barbara, Savoia, Paola

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PARP1 Inhibitor and Trabectedin Combination Does Not Increase Tumor Mutational Burden in Advanced Sarcomas-A Preclinical and Translational Study von Pignochino, Ymera, Crisafulli, Giovanni, Giordano, Giorgia, Merlini, Alessandra, Berrino, Enrico, Centomo, Maria Laura, Chiabotto, Giulia, Brusco, Silvia, Basiricò, Marco, Maldi, Elena, Pisacane, Alberto, Leuci, Valeria, Sangiolo, Dario, D'Ambrosio, Lorenzo, Aglietta, Massimo, Kasper, Bernd, Bardelli, Alberto, Grignani, Giovanni

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Síndrome de Kabuki con artritis reumatoide: primer caso reportado von Hernández, Rocío, Brusco, Isabel, Marcantoni, María Beatriz, Cervetto, Vanesa, Osler, Valeria González, Lacapra, María Emilia

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Bilaterally cleft lip and bilateral thumb polydactyly with triphalangeal component in a patient with two De novo deletions of HSA 4q32 and 4q34 involving PDGFC, GRIA2, and FBXO8 ge... von Calcia, Alessandro, Gai, Giorgia, Di Gregorio, Eleonora, Talarico, Flavia, Naretto, Valeria G., Migone, Nicola, Pepe, Ernesto, Grosso, Enrico, Brusco, Alfredo

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Large cryptic genomic rearrangements with apparently normal karyotypes detected by array-CGH von Di Gregorio, Eleonora, Savin, Elisa, Biamino, Elisa, Belligni, Elga Fabia, Naretto, Valeria Giorgia, D'Alessandro, Gaetana, Gai, Giorgia, Fiocchi, Franco, Calcia, Alessandro, Mancini, Cecilia, Giorgio, Elisa, Cavalieri, Simona, Talarico, Flavia, Pappi, Patrizia, Gandione, Marina, Grosso, Monica, Asnaghi, Valentina, Restagno, Gabriella, Mandrile, Giorgia, Botta, Giovanni, Silengo, Margherita Cirillo, Grosso, Enrico, Ferrero, Giovanni Battista, Brusco, Alfredo

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Bilaterally cleft lip and bilateral thumb polydactyly with triphalangeal component in a patient with two De novo deletions of HSA 4q32 and 4q34 involving PDGFC , GRIA 2 , and FBXO... von Calcia, Alessandro, Gai, Giorgia, Di Gregorio, Eleonora, Talarico, Flavia, Naretto, Valeria G., Migone, Nicola, Pepe, Ernesto, Grosso, Enrico, Brusco, Alfredo

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Erratum to: Medication prescription and adherence disparities in non valvular atrial fibrillation patients: an Italian portrait from the ARAPACIS study von Raparelli, Valeria, Proietti, Marco, Buttà, Carmelo, Di Giosia, Paolo, Sirico, Domenico, Gobbi, Paolo, Corrao, Salvatore, Davì, Giovanni, Vestri, Anna Rita, Perticone, Francesco, Corazza, Gino Roberto, Violi, Francesco, Basili, Stefania

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