Communicating the diagnosis of Klinefelter syndrome to children and adolescents: when, how, and who? von Aliberti, L., Gagliardi, I., Bigoni, S., Lupo, S., Caracciolo, S., Ferlini, A., Isidori, A. M., Zatelli, M. C., Ambrosio, M. R.

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ABSTRACT 822: PERTUSSIS SYNDROME A PREVENTABLE INFECTIOUS DISEASE DEMANDING EMERGENCY AND PICU RESOURCES von Piva, J., Pinheiro, F., Ferlini, R., Picolli, R., Lago, P., Baldasso, E., Andreolio, C., Trotta, E.A., Carvalho, P.R.

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ABSTRACT 187: DEXMEDETOMIDINE INFUSION IN A PEDIATRIC POPULATION von Piva, J., Andreolio, C., Ferlini, R., Pinheiro, F., Baldassol, E., Lago, P., Librelato, G., Piccoli, R., Trotta, E.A., Carvalho, P.R.

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MUSCLE FUNCTION & HOMEOSTASIS / MOLECULAR THERAPEUTIC APPROACHES von Falzarano, M., Spedicato, N., Margutti, A., Dani, R. El, Rossi, R., Zia, S., Reschiglian, P., Roda, B., Grilli, A., Bicciato, S., Ferlini, A.

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Starch thickening of human milk is ineffective in reducing the gastroesophageal reflux in preterm infants: A crossover study using intraluminal impedance von Corvaglia, Luigi, Ferlini, Marianna, Rotatori, Raffaella, Paoletti, Vittoria, Alessandroni, Rosina, Cocchi, Guido, Faldella, Giacomo

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ABSTRACT 459: HIGH SURVIVAL RATE IS THE RULE FOR CHILDREN WITH ACUTE VIRAL BRONCHIOLITIS SUBMITTED TO MECHANICAL VENTILATION von Piva, J., Ferlini, R., Pinheiro, F., Baldasso, E., Andreolio, C., Lago, P., Giorgio, C., Carvalho, P., Trotta, E.

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Probing chromatin structure in the early phases of apoptosis von Ferlini, C., Biselli, R., Scambia, G., Fattorossi, A.

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MUSCLE FUNCTION & HOMEOSTASIS / MOLECULAR THERAPEUTIC APPROACHES: P.66 Cell sorting and characterization of urine-derived stem cells (USCs) using the novel technology Celector von Falzarano, M., Spedicato, N., Margutti, A., Dani, R. El, Rossi, R., Zia, S., Reschiglian, P., Roda, B., Grilli, A., Bicciato, S., Ferlini, A.

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Mother and daughter with Kenny-Caffey syndrome: the adult phenotype von Tonelli, L., Sanchini, M., Margutti, A., Buldrini, B., Superti-Furga, A., Ferlini, A., Selvatici, R., Bigoni, S.

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DMD/BMD - GENETICS von Selvatici, R., Rossi, R., Fang, M., Lu, J., Sansone, V., Falzarano, M., Gualandi, F., Bello, L., Pegoraro, E., Ferlini, A.

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DMD/BMD - GENETICS von Mietto, M., Fabris, M., Bonaccorso, R., Previtali, S., Zambon, A., Gualandi, F., Rossi, R., Falzarano, M., Ferlini, A.

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Fractional Flow Reserve–Guided PCI as Compared with Coronary Bypass Surgery von Van Belle, Eric, Patel, Manesh, Davies, Justin, Rosenblum, Adam L., Pack, Quinn R., Feldman, Daniel, Nicolas, Johny, Dangas, George, Ferlini, Marco, Munafò, Andrea, Visconti, L. Oltrona, Fearon, William F., Zimmermann, Frederik M., Pijls, Nico H.J.

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APPLICATION OF NEXT GENERATION TECHNOLOGIES von Selvatici, R., Neri, M., Fortunato, F., Rossi, R., D'Amico, A., Bertini, E., Pane, M., Mercuri, E., Fini, S., Bigoni, S., Gualandi, F., Ferlini, A.

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NEW GENES AND DISEASES / NGS & RELATED TECHNIQUES von Selvatici, R., Fang, M., Falzarano, M., Gualandi, F., Delin, S., Bensemmane, S., Shatillo, A., Bello, L., Pegoraro, E., Ferlini, A.

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DMD/BMD - GENETICS: EP.117 Whole genome sequencing and RNA analysis allow genetic diagnosis of DMD atypical mutations von Selvatici, R., Rossi, R., Fang, M., Lu, J., Sansone, V., Falzarano, M., Gualandi, F., Bello, L., Pegoraro, E., Ferlini, A.

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DMD/BMD - GENETICS: EP.113 Lack of correlation between DMD exon 2 duplication splicing choices and phenotype severity von Mietto, M., Fabris, M., Bonaccorso, R., Previtali, S., Zambon, A., Gualandi, F., Rossi, R., Falzarano, M., Ferlini, A.

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Autophagy induction in atrophic muscle cells requires ULK1 activation by TRIM32 through unanchored K63-linked polyubiquitin chains von Di Rienzo, M, Antonioli, M, Fusco, C, Liu, Y, Mari, M, Orhon, I, Refolo, G, Germani, F, Corazzari, M, Romagnoli, A, Ciccosanti, F, Mandriani, B, Pellico, M T, De La Torre, R, Ding, H, Dentice, M, Neri, M, Ferlini, A, Reggiori, F, Kulesz-Martin, M, Piacentini, M, Merla, G, Fimia, G M

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APPLICATION OF NEXT GENERATION TECHNOLOGIES: EP.312 Whole exome sequencing and whole Genome sequencing re-analysis to identify the genetic causes of undiagnosed neuromuscular pheno... von Selvatici, R., Neri, M., Fortunato, F., Rossi, R., D'Amico, A., Bertini, E., Pane, M., Mercuri, E., Fini, S., Bigoni, S., Gualandi, F., Ferlini, A.

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A single NGS‐based assay covering the entire genomic sequence of the DMD gene facilitates diagnostic and newborn screening confirmatory testing von Nallamilli, Babi R. R., Chaubey, Alka, Valencia, C. A., Stansberry, Leah, Behlmann, Andrea M., Ma, Zeqiang, Mathur, Abhinav, Shenoy, Suresh, Ganapathy, Vidya, Jagannathan, Lakshmanan, Ramachander, Vinish, Ferlini, Alessandra, Bean, Lora, Hegde, Madhuri

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NEW GENES AND DISEASES / NGS & RELATED TECHNIQUES: P.327 Whole exome and whole genome sequencing for the genetic diagnosis of dystrophinopathies von Selvatici, R., Fang, M., Falzarano, M., Gualandi, F., Delin, S., Bensemmane, S., Shatillo, A., Bello, L., Pegoraro, E., Ferlini, A.

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