Non-invasive CPAP in mild and moderate ARDS secondary to SARS-CoV-2 von Pagano, A., Porta, G., Bosso, G., Allegorico, E., Serra, C., Dello Vicario, F., Minerva, V., Russo, T., Altruda, C., Arbo, P., Mercurio, V., Numis, F.G.

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Blood lactate in mild and moderate ARDS secondary to SARS COV 2 von Pagano, A., Porta, G., Bosso, G., Allegorico, E., Serra, C., Mercurio, V., Sansone, G., Orefice, S., Numis, F.G.

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Application and internal validation of lung ultrasound score in COVID-19 setting: The ECOVITA observational study von Rinaldi, L., Lugarà, M., Simeon, V., Perrotta, F., Romano, C., Iadevaia, C., Sagnelli, C., Monaco, L., Altruda, C., Fascione, M.C., Restivo, L., Scognamiglio, U., Laganà, N., Nevola, R., Oliva, G., Coppola, M.G., Acierno, C., Masini, F., Pinotti, E., Allegorico, E., Tamburrini, S., Vitiello, G., Niosi, M., Burzo, M.L., Franci, G., Perrella, A., Signoriello, G., Frusci, V., Mancarella, S., Loche, G., Pellicano, G.F., Berretta, M., Calabria, G., Pietropaolo, L., Numis, F.G., Coppola, N., Corcione, A., Marfella, R., Adinolfi, L.E., Bianco, A., Sasso, F.C., de Sio, I.

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Association between vitamin D receptor gene polymorphisms and tubular citrate handling in calcium nephrolithiasis von Mossetti, G., Vuotto, P., Rendina, D., Numis, F. G., Viceconti, R., Giordano, F., Cioffi, M., Scopacasa, F., Nunziata, V.

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Biochemical markers of bone turnover, serum levels of interleukin-6/interleukin-6 soluble receptor and bisphosphonate treatment in erdheim-chester disease von MOSSETTI, G, RENDINA, D, NUMIS, F. G, SOMMA, P, POSTIGLIONE, L, NUNZIATA, V

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Raloxifene administration in post‐menopausal women with osteoporosis: effect of different BsmI vitamin D receptor genotypes von Palomba, Stefano, Numis, Fabio Giuliano, Mossetti, Giuseppe, Rendina, Domenico, Vuotto, Pietro, Russo, Tiziana, Zullo, Fulvio, Nappi, Carmine, Nunziata, Vincenzo

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Clodronate treatment reduces serum levels of interleukin-6 soluble receptor in Paget's disease of bone von RENDINA, D, POSTIGLIONE, L, VUOTTO, P, NUMIS, F. G, DI DOMENICO, G, VICECONTI, R, MOSSETTI, G, NUNZIATA, V

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Abnormal vascular reactivity in growth hormone deficiency von CAPALDO, Brunella, GUARDASOLE, Vincenzo, PARDO, Francesco, MATARAZZO, Margherita, DI RELLA, Francesca, NUMIS, Fabio, MEROLA, Bartolomeo, LONGOBARDI, Salvatore, SACCA, Luigi

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Effectiveness of alendronate treatment in postmenopausal women with osteoporosis: relationship with BsmI vitamin D receptor genotypes von Palomba, Stefano, Numis, Fabio Giuliano, Mossetti, Giuseppe, Rendina, Domenico, Vuotto, Pietro, Russo, Tiziana, Zullo, Fulvio, Nappi, Carmine, Nunziata, Vincenzo

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IGF-I generation test: Effects on body composition von Longobardi, S, Angelillo, N, D'Amico, D, De Felice, D, Dentico, C, Di Costanzo, B, Di Rella, F, Lombardi, G, Merola, B, Numis, F, Sabatella, M

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GH secretion after pharmacological tests (GHRH, clonidine and GHRH+pyridostigmine) both in GH deficient patients and severe obesity von Orio, F, Caggiano, D, Cittadini, A, Dentico, C, Di Rella, F, Di Seranno, A, Longobardi, S, Merola, B, Numis, FG, Orio, F, Tenuta, M

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Assessing Early Severity of Hypoxic-Ischemic Encephalopathy: The Role of Electroencephalogram Background in Addition to Sarnat Exam von Cornet, Marie-Coralie, Numis, Adam L., Monsell, Sarah E., Chan, Natalie H., Gonzalez, Fernando F., Comstock, Bryan A., Juul, Sandra E., Wusthoff, Courtney J., Wu, Yvonne W., Glass, Hannah C.

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Risk of seizures in neonates with hypoxic-ischemic encephalopathy receiving hypothermia plus erythropoietin or placebo von Glass, Hannah C., Wusthoff, Courtney J., Comstock, Bryan A., Numis, Adam L., Gonzalez, Fernando F., Maitre, Nathalie, Massey, Shavonne L., Mayock, Dennis E., Mietzsch, Ulrike, Natarajan, Niranjana, Sokol, Gregory M., Bonifacio, Sonia L., Van Meurs, Krisa P., Thomas, Cameron, Ahmad, Kaashif A., Heagerty, Patrick J., Juul, Sandra E., Wu, Yvonne W.

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Association of EEG Background and Neurodevelopmental Outcome in Neonates With Hypoxic-Ischemic Encephalopathy Receiving Hypothermia von Glass, Hannah C, Numis, Adam L, Comstock, Bryan A, Gonzalez, Fernando F, Mietzsch, Ulrike, Bonifacio, Sonia Lomeli, Massey, Shavonne, Thomas, Cameron, Natarajan, Niranjana, Mayock, Dennis E, Sokol, Gregory M, Van Meurs, Krisa P, Ahmad, Kaashif A, Maitre, Nathalie, Heagerty, Patrick J, Juul, Sandra E, Wu, Yvonne W, Wusthoff, Courtney J

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De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial Dysmorphism von Guillen Sacoto, Maria J., Tchasovnikarova, Iva A., Torti, Erin, Forster, Cara, Andrew, E. Hallie, Anselm, Irina, Baranano, Kristin W., Briere, Lauren C., Cohen, Julie S., Craigen, William J., Cytrynbaum, Cheryl, Ekhilevitch, Nina, Elrick, Matthew J., Fatemi, Ali, Fraser, Jamie L., Gallagher, Renata C., Guerin, Andrea, Haynes, Devon, High, Frances A., Inglese, Cara N., Kiss, Courtney, Koenig, Mary Kay, Krier, Joel, Lindstrom, Kristin, Marble, Michael, Meddaugh, Hannah, Moran, Ellen S., Morel, Chantal F., Mu, Weiyi, Muller, Eric A., Nance, Jessica, Natowicz, Marvin R., Numis, Adam L., Ostrem, Bridget, Pappas, John, Stafstrom, Carl E., Streff, Haley, Sweetser, David A., Szybowska, Marta, Walker, Melissa A., Wang, Wei, Weiss, Karin, Weksberg, Rosanna, Wheeler, Patricia G., Yoon, Grace, Kingston, Robert E., Juusola, Jane

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Leveraging expertise and optimizing clinical research: Initial success of a pediatric epilepsy surgery collaborative von Berl, Madison M., Koop, Jennifer I., Ailion, Alyssa, Bearden, Donald J., Boyer, Katrina, Cooper, Crystal M., Decrow, Amanda M., Duong, Priscilla H., Espe‐Pfeifer, Patricia, Gabriel, Marsha, Hodges, Elise, Marshall, David F., McNally, Kelly A., Molnar, Andrew E., Olsen, Emily K., Ono, Kim E., Patrick, Kristina E., Paul, Brianna M., Romain, Jonathan, Sepeta, Leigh N., Stilp, Rebecca L. H., Wilkening, Greta N., Zaccariello, Michael, Zelko, Frank, Perry, M. Scott, Alexander, Allyson L., Andrade‐Machado, Rene, Armstrong, Dallas, Auguste, Kurtis, Bolton, Jeffrey, Ciliberto, Michael, Coryell, Jason, Depositario‐Cabacar, Dewi, Eschbach, Krista, Gaillard, William D., Gedela, Satya, Gonzalez‐Giraldo, Ernesto, Grinspan, Zachary, Hauptman, Jason, Javarayee, Pradeep, Karia, Samir, Manuel, Chad Mac, Marashly, Ahmad, McCormack, Michael J., McNamara, Nancy, Nangia, Srishti, Novotny, Edward John, Numis, Adam, Olaya, Joffre, Oluigbo, Chima, Ostendorf, Adam, Reddy, Shilpa B., Romanowski, Erin Fedak, Samanta, Debopam, Shrey, Daniel, Singh, Rani, Sullivan, Joseph, Tatachar, Priya, Wong‐Kisiel, Lily

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The Epilepsy Genetics Initiative: Systematic reanalysis of diagnostic exomes increases yield von Berkovic, Samuel F., Goldstein, David B., Heinzen, Erin L., Laughlin, Brandon L., Lowenstein, Daniel H., Lubbers, Laura, Stewart, Randall, Whittemore, Vicky, Angione, Kaitlin, Bazil, Carl W., Bier, Louise, Bluvstein, Judith, Brimble, Elise, Campbell, Colleen, Cavalleri, Gianpiero, Chambers, Chelsea, Choi, Hyunmi, Cilio, Maria Roberta, Ciliberto, Michael, Cornes, Susannah, Delanty, Norman, Demarest, Scott, Devinsky, Orrin, Dlugos, Dennis, Dubbs, Holly, Dugan, Patricia, Ernst, Michelle E., Gibbons, Melissa, Goodkin, Howard P., Helbig, Ingo, Jansen, Laura, Johnson, Kaleas, Joshi, Charuta, Lippa, Natalie C., Marsh, Eric, Martinez, Alejandro, Millichap, John, Mulhern, Maureen S., Numis, Adam, Park, Kristen, Pippucci, Tommaso, Poduri, Annapurna, Porter, Brenda, Regan, Brigid, Sands, Tristan T., Scheffer, Ingrid E., Schreiber, John M., Sheidley, Beth, Singhal, Nilika, Smith, Lacey, Sullivan, Joseph, Taylor, Alan, Tolete, Patricia, Afgani, Tahseen M., Aggarwal, Vimla, Burgess, Rosemary, Dixon‐Salazar, Tracy, Hemati, Parisa, Milder, Julie, Petrovski, Slavé, Revah‐Politi, Anya, Stong, Nicholas

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Predictors of Death or Severe Impairment in Neonates With Hypoxic-Ischemic Encephalopathy von Glass, Hannah C, Wood, Thomas R, Comstock, Bryan A, Numis, Adam L, Bonifacio, Sonia L, Cornet, Marie-Coralie, Gonzalez, Fernando F, Morell, Adriana, Kolnik, Sarah E, Li, Yi, Mathur, Amit, Mietzsch, Ulrike, Wu, Tai-Wei, Wusthoff, Courtney J, Thoresen, Marianne, Heagerty, Patrick J, Juul, Sandra E, Wu, Yvonne W

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De novo variants in the alternative exon 5 of SCN8A cause epileptic encephalopathy

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Responsive neurostimulation for treatment of pediatric drug-resistant epilepsy von Singhal, Nilika S, Numis, Adam L, Lee, Morgan B, Chang, Edward F, Sullivan, Joseph E, Auguste, Kurtis I, Rao, Vikram R

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