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Intimate Partner Violence: Piloting an E-Module for Pediatric Staff von Howard, Mary Beth, Fornari, Marci J, Colson, Cindy D, Ebner, Megan, Jarvis, Lenore R

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Evaluation of Missing Prehospital Physiological Values in Injured Children and Adolescents von Sullivan, Travis M., Milestone, Zachary P., Colson, Cindy D., Tempel, Peyton E., Gestrich-Thompson, Waverly V., Burd, Randall S.

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56 Evaluation of a Smartphone Application as a Method for Calculating Total Body Surface Area Burned von Colson, Cindy D, Alberto, Emily A, Milestone, Zachary P, Batra, Nikita, Salvadore, Tyler, Fooladi, Hadi, Cleary, Kevin, Izem, Rima, Burd, Randall S

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Wiedemann‐Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French cases von Baer, S., Afenjar, A., Smol, T., Piton, A., Gérard, B., Alembik, Y., Bienvenu, T., Boursier, G., Boute, O., Colson, C., Cordier, M.‐P., Cormier‐Daire, V., Delobel, B., Doco‐Fenzy, M., Duban‐Bedu, B., Fradin, M., Geneviève, D., Goldenberg, A., Grelet, M., Haye, D., Heron, D., Isidor, B., Keren, B., Lacombe, D., Lèbre, A.‐S., Lesca, G., Masurel, A., Mathieu‐Dramard, M., Nava, C., Pasquier, L., Petit, A., Philip, N., Piard, J., Rondeau, S., Saugier‐Veber, P., Sukno, S., Thevenon, J., Van‐Gils, J., Vincent‐Delorme, C., Willems, M., Schaefer, E., Morin, G.

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Functional analysis of TLK2 variants and their proximal interactomes implicates impaired kinase activity and chromatin maintenance defects in their pathogenesis von Pavinato, Lisa, Pippucci, Tommaso, Prota, Valentina, Carli, Diana, Giorgio, Elisa, Radio, Francesca Clementina, Antona, Vincenzo, Giuffrè, Mario, Ranguin, Kara, Colson, Cindy, De Rubeis, Silvia, Villamor Payà, Marina, Dimartino, Paola, Buxbaum, Joseph D, Ferrero, Giovanni Battista, Tartaglia, Marco, Martinelli, Simone, Stracker, Travis H, Brusco, Alfredo, Sanchiz Calvo, Maria, Andreoli, Cristina, Gay, Marina, Vilaseca, Marta, Arauz-Garofalo, Gianluca, Ciolfi, Andrea, Bruselles, Alessandro

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Atteintes articulaires du syndrome de Noonan. Étude descriptive et rétrospective d’une population pédiatrique von Le Quellec, Aurore, Edouard, Thomas, Audebert-Bellanger, Séverine, Pouzet, Antoine, Bourdet, Karine, Colson, Cindy, Oriot, Charlotte, Poignant, Sylvaine, Saraux, Alain, Devauchelle-Pensec, Valérie

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Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome von Tessadori, Federico, Duran, Karen, Knapp, Karen, Fellner, Matthias, Smithson, Sarah, Beleza Meireles, Ana, Elting, Mariet W, Waisfisz, Quinten, O'Donnell-Luria, Anne, Nowak, Catherine, Douglas, Jessica, Ronan, Anne, Brunet, Theresa, Kotzaeridou, Urania, Svihovec, Shayna, Saenz, Margarita S, Thiffault, Isabelle, Del Viso, Florencia, Devine, Patrick, Rego, Shannon, Tenney, Jessica, van Haeringen, Arie, Ruivenkamp, Claudia Antoinette Laetitia, Koene, Saskia, Robertson, Stephen P, Deshpande, Charulata, Pfundt, Rolph, Verbeek, Nienke, van de Kamp, Jiddeke M, Weiss, Janneke M.M, Ruiz, Anna, Gabau, Elisabeth, Banne, Ehud, Pepler, Alexander, Bottani, Armand, Laurent, Sacha, Guipponi, Michel, Bijlsma, Emilia, Bruel, Ange-Line, Sorlin, Arthur, Willis, Mary, Powis, Zoe, Smol, Thomas, Vincent-Delorme, Catherine, Baralle, Diana, Colin, Estelle, Revencu, Nicole, Calpena, Eduardo, Wilkie, Andrew O.M, Chopra, Maya, Cormier-Daire, Valerie, Keren, Boris, Afenjar, Alexandra, Niceta, Marcello, Terracciano, Alessandra, Specchio, Nicola, Tartaglia, Marco, Rio, Marlene, Barcia, Giulia, Rondeau, Sophie, Colson, Cindy, Bakkers, Jeroen, Mace, Peter D, Bicknell, Louise S, van Haaften, Gijs, Universitat Autònoma de Barcelona

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