Is there still space for the implementation of antisepsis and disinfection to prevent rotavirus and norovirus gastroenteritis outbreaks? von Protano, C, Vitali, M, Raitano, A, Sancin, A, Agolini, G

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Prevention of infection spreading by cleaning and disinfecting : different approaches and difficulties in communicating: Staphylococcal Infections von VITALI, M, AGOLINI, G

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Prevention of infection spreading by cleaning and disinfecting: Different approaches and difficulties in communicating von Vitali, Matteo, Agolini, Giuliano

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Iris alteration using mechanical iris retractors von Tognetto, Daniele, Agolini, Giorgio, Grandi, Giorgio, Ravalico, Giuseppe

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Intravenous Nutritional Support During Pregnancy von Agolini, G., Fumi, L.

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Effect of phenolic and chlorine disinfectants on hepatitis C virus binding and infectivity von Agolini, Giuliano, Russo, Antonello, Clementi, Massimo

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Spontaneous dislocation into the vitreous of a poly(methyl methacrylate) disc lens 9 years after surgery von TOGNETTO, D, AGOLINI, G, RAVALICO, G

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Novel congenital disorder of O-linked glycosylation caused by GALNT2 loss of function von Zilmer, Monica, Edmondson, Andrew C., Khetarpa, Sumeet A., Alesi, Viola, Zaki, Maha S., Rostasy, Kevin, Madsen, Camilla G., Lepri, Francesca R., Sinibaldi, Lorenzo, Cusmai, Raffaella, Novelli, Antonio, Issa, Mahmoud Y., Fenger, Christina D., Abou Jamra, Rami, Reutter, Heiko, Briuglia, Silvana, Agolini, Emanuele, Hansen, Lars, Petaja-Repo, Ulla E., Hintze, John, Raymond, Kimiyo M., Liedtke, Kristen, Stanley, Valentina, Musaev, Damir, Gleeson, Joseph G., Vitali, Cecilia, O'Brien, W. Timothy, Gardella, Elena, Rubboli, Guido, Rader, Daniel J., Schjoldager, Katrine T., Moller, Rikke S.

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Pathogenic Variants in GPC4 Cause Keipert Syndrome von Amor, David J., Stephenson, Sarah E.M., Mustapha, Mirna, Mensah, Martin A., Ockeloen, Charlotte W., Lee, Wei Shern, Tankard, Rick M., Phelan, Dean G., Shinawi, Marwan, de Brouwer, Arjan P.M., Pfundt, Rolph, Dowling, Cari, Toler, Tomi L., Sutton, V. Reid, Agolini, Emanuele, Rinelli, Martina, Capolino, Rossella, Martinelli, Diego, Zampino, Giuseppe, Dumić, Miroslav, Reardon, William, Shaw-Smith, Charles, Leventer, Richard J., Delatycki, Martin B., Kleefstra, Tjitske, Mundlos, Stefan, Mortier, Geert, Bahlo, Melanie, Allen, Nicola J., Lockhart, Paul J.

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Pregnancy in women with Hereditary Angioedema due to C1-inhibitor deficiency: Results from the ITACA cohort study on outcome of mothers and children with in utero exposure to plasm... von Triggianese, P., Senter, R., Petraroli, A., Zoli, A., Lo Pizzo, M., Bignardi, D., Di Agosta, E., Agolini, S., Arcoleo, F., Rossi, O., Modica, S., Greco, E., Chimenti, M. S., Spadaro, G., De Carolis, C., Cancian, M.

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Widening the infantile hypotonia with psychomotor retardation and characteristic Facies-1 Syndrome's clinical and molecular spectrum through NALCN in-silico structural analysis von Vecchio, Davide, Macchiaiolo, Marina, Gonfiantini, Michaela V, Panfili, Filippo M, Petrizzelli, Francesco, Liorni, Niccolò, Cortellessa, Fabiana, Sinibaldi, Lorenzo, Rana, Ippolita, Agolini, Emanuele, Cocciadiferro, Dario, Colantoni, Nicole, Semeraro, Michela, Rizzo, Cristiano, Deodati, Annalisa, Cotugno, Nicola, Caggiano, Serena, Verrillo, Elisabetta, Nucci, Carlotta G, Alkan, Serpil, Saraiva, Jorge M, De Sá, Joaquim, Almeida, Pedro M, Krishna, Jayanth, Buonuomo, Paola S, Martinelli, Diego, Dionisi Vici, Carlo, Caputo, Viviana, Bartuli, Andrea, Novelli, Antonio, Mazza, Tommaso

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Progressive liver, kidney, and heart degeneration in children and adults affected by TULP3 mutations von Devane, John, Ott, Elisabeth, Olinger, Eric G., Epting, Daniel, Decker, Eva, Friedrich, Anja, Bachmann, Nadine, Renschler, Gina, Eisenberger, Tobias, Briem-Richter, Andrea, Grabhorn, Enke Freya, Powell, Laura, Wilson, Ian J., Rice, Sarah J., Miles, Colin G., Wood, Katrina, Trivedi, Palak, Hirschfield, Gideon, Pietrobattista, Andrea, Wohler, Elizabeth, Mezina, Anya, Sobreira, Nara, Agolini, Emanuele, Maggiore, Giuseppe, Dahmer-Heath, Mareike, Yilmaz, Ali, Boerries, Melanie, Metzger, Patrick, Schell, Christoph, Grünewald, Inga, Konrad, Martin, König, Jens, Schlevogt, Bernhard, Sayer, John A., Bergmann, Carsten

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Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype von Breen, Michael S., Garg, Paras, Tang, Lara, Mendonca, Danielle, Levy, Tess, Barbosa, Mafalda, Arnett, Anne B., Kurtz-Nelson, Evangeline, Agolini, Emanuele, Battaglia, Agatino, Chiocchetti, Andreas G., Freitag, Christine M., Garcia-Alcon, Alicia, Grammatico, Paola, Hertz-Picciotto, Irva, Ludena-Rodriguez, Yunin, Moreno, Carmen, Novelli, Antonio, Parellada, Mara, Pascolini, Giulia, Tassone, Flora, Grice, Dorothy E., Di Marino, Daniele, Bernier, Raphael A., Kolevzon, Alexander, Sharp, Andrew J., Buxbaum, Joseph D., Siper, Paige M., De Rubeis, Silvia

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Identification of a robust DNA methylation signature for Fanconi anemia von Pagliara, Daria, Ciolfi, Andrea, Pedace, Lucia, Haghshenas, Sadegheh, Ferilli, Marco, Levy, Michael A., Miele, Evelina, Nardini, Claudia, Cappelletti, Camilla, Relator, Raissa, Pitisci, Angela, De Vito, Rita, Pizzi, Simone, Kerkhof, Jennifer, McConkey, Haley, Nazio, Francesca, Kant, Sarina G., Di Donato, Maddalena, Agolini, Emanuele, Matraxia, Marta, Pasini, Barbara, Pelle, Alessandra, Galluccio, Tiziana, Novelli, Antonio, Barakat, Tahsin Stefan, Andreani, Marco, Rossi, Francesca, Mecucci, Cristina, Savoia, Anna, Sadikovic, Bekim, Locatelli, Franco, Tartaglia, Marco

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De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders von Jia, Xiangbin, Zhang, Shujie, Tan, Senwei, Du, Bing, He, Mei, Qin, Haisong, Chen, Jia, Duan, Xinyu, Luo, Jingsi, Chen, Fei, Ouyang, Luping, Wang, Jian, Chen, Guodong, Yu, Bin, Zhang, Ge, Zhang, Zimin, Lyu, Yongqing, Huang, Yi, Jiao, Jian, Chen, Jin Yun Helen, Swoboda, Kathryn J, Agolini, Emanuele, Novelli, Antonio, Leoni, Chiara, Zampino, Giuseppe, Cappuccio, Gerarda, Brunetti-Pierri, Nicola, Gerard, Benedicte, Ginglinger, Emmanuelle, Richer, Julie, McMillan, Hugh, White-Brown, Alexandre, Hoekzema, Kendra, Bernier, Raphael A, Kurtz-Nelson, Evangeline C, Earl, Rachel K, Meddens, Claartje, Alders, Marielle, Fuchs, Meredith, Caumes, Roseline, Brunelle, Perrine, Smol, Thomas, Kuehl, Ryan, Day-Salvatore, Debra-Lynn, Monaghan, Kristin G, Morrow, Michelle M, Eichler, Evan E, Hu, Zhengmao, Yuan, Ling, Tan, Jieqiong, Xia, Kun, Shen, Yiping, Guo, Hui

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Biallelic hypomorphic variants in ALDH1A2 cause a novel lethal human multiple congenital anomaly syndrome encompassing diaphragmatic, pulmonary, and cardiovascular defects von Beecroft, Sarah J., Ayala, Marcos, McGillivray, George, Nanda, Vikas, Agolini, Emanuele, Novelli, Antonio, Digilio, Maria C., Dotta, Andrea, Carrozzo, Rosalba, Clayton, Joshua, Gaffney, Lydia, McLean, Catriona A., Ng, Jessica, Laing, Nigel G., Matteson, Paul, Millonig, James, Ravenscroft, Gianina

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Monoallelic de novo variants in DDX17 cause a neurodevelopmental disorder von Seaby, Eleanor G, Godwin, Annie, Meyer-Dilhet, Géraldine, Clerc, Valentine, Grand, Xavier, Fletcher, Tia, Monteiro, Laloe, Kerkhofs, Martijn, Carelli, Valerio, Palombo, Flavia, Seri, Marco, Olivucci, Giulia, Grippa, Mina, Ciaccio, Claudia, D'Arrigo, Stefano, Iascone, Maria, Bermudez, Marion, Fischer, Jan, Di Donato, Nataliya, Goesswein, Sophie, Leung, Marco L, Koboldt, Daniel C, Myers, Cortlandt, Arnadottir, Gudny Anna, Stefansson, Kari, Sulem, Patrick, Goldberg, Ethan M, Bruel, Ange-Line, Tran Mau Them, Frederic, Willems, Marjolaine, Bjornsson, Hans Tomas, Hognason, Hakon Bjorn, Thorolfsdottir, Eirny Tholl, Agolini, Emanuele, Novelli, Antonio, Zampino, Giuseppe, Onesimo, Roberta, Lachlan, Katherine, Baralle, Diana, Rehm, Heidi L, O'Donnell-Luria, Anne, Courchet, Julien, Guille, Matt, Bourgeois, Cyril F, Ennis, Sarah

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Pilot Study of Warfarin Genotype Polymorphisms in Pediatric Patients with Ventricular Assist Devices von Iodice, F, Baban, A, Di Molfetta, A, Di Chiara, L, Novelli, A, Agolini, E, Amodeo, A, Testa, G

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Structural modeling of a novel TERC variant in a patient with aplastic anemia and short telomeres von Rinelli, M., Bellacchio, E., Berardinelli, F., Pascolini, G., Grammatico, P., Sgura, A., Iori, A. P., Quattrocchi, L., Novelli, A., Majore, S., Agolini, E.

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Correction to “Posterior fossa ependymoma in neurodevelopmental syndrome caused by a de novo germline pathogenic POLR2A variant”

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