Video-EEG monitoring in newborns with hypoxic-ischemic encephalopathy treated with hypothermia von NASH, K. B, BONIFACIO, S. L, GLASS, H. C, SULLIVAN, J. E, BARKOVICH, A. J, FERRIERO, D. M, CILIO, M. R

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PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilati... von Matera, I, Bachetti, T, Puppo, F, Di Duca, M, Morandi, F, Casiraghi, G M, Cilio, M R, Hennekam, R, Hofstra, R, Schöber, J G, Ravazzolo, R, Ottonello, G, Ceccherini, I

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Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancy von MADIA, F, STRIANO, P, MINETTI, C, ZARA, F, GENNARO, E, MALACARNE, M, PARAVIDINO, R, BIANCHERI, R, BUDETTA, M, CILIO, M. R, GAGGERO, R, PIERLUIGI, M

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Early-onset seizure variant of Rett syndrome: Definition of the clinical diagnostic criteria von Artuso, R, Mencarelli, M.A, Polli, R, Sartori, S, Ariani, F, Pollazzon, M, Marozza, A, Cilio, M.R, Specchio, N, Vigevano, F, Vecchi, M, Boniver, C, Dalla Bernardina, B, Parmeggiani, A, Buoni, S, Hayek, G, Mari, F, Renieri, A, Murgia, A

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Vigabatrin Versus ACTH as First‐Line Treatment for Infantile Spasms: A Randomized, Prospective Study von Vigevano, Pederico, Cilio, Maria Roberta

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Dorsal Brain Stem Syndrome: MR Imaging Location of Brain Stem Tegmental Lesions in Neonates with Oral Motor Dysfunction von QUATTROCCHI, C. C, LONGO, D, DELFINO, L. N, CILIO, M. R, PIERSIGILLI, F, CAPUA, M. D, SEGANTI, G, DANHAIVE, O, FARIELLO, G

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Congenital central hypoventilation syndrome: genotype-phenotype correlation in parents of affected children carrying a PHOX2B expansion mutation von Parodi, S, Vollono, C, Baglietto, MP, Balestri, M, Di Duca, M, Landri, PA, Ceccherini, I, Ottonello, G, Cilio, MR

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Anticonvulsant action and long-term effects of gabapentin in the immature brain von Cilio, M.R, Bolanos, A.R, Liu, Z, Schmid, R, Yang, Y, Stafstrom, C.E, Mikati, M.A, Holmes, G.L

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Homozygosity mapping of Hallervorden–Spatz syndrome to chromosome 20p12.3–p13 von Taylor, Todd D., Litt, Michael, Kramer, Patricia, Pandolfo, Massimo, Angelini, Lucia, Nardocci, Nardo, Davis, Suzanne, Pineda, M., Hattori, Haruo, Flett, Peter J., Cilio, M. Roberta, Bertini, Enrico, Hayflick, Susan J.

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Childhood refractory focal epilepsy following acute febrile encephalopathy von Specchio, N., Fusco, L., Claps, D., Trivisano, M., Longo, D., Cilio, M. R., Valeriani, M., Cusmai, R., Cappelletti, S., Gentile, S., Fariello, G., Specchio, L. M., Vigevano, F.

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Reduced Neurogenesis after Neonatal Seizures von McCabe, Bridget K, Silveira, Diosely C, Cilio, Maria Roberta, Cha, Byung Ho, Liu, Xianzeng, Sogawa, Yoshimi, Holmes, Gregory L

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Long-term effects of neonatal seizures: a behavioral, electrophysiological, and histological study von Huang, L.-T, Cilio, M.R, Silveira, D.C, McCabe, B.K, Sogawa, Y, Stafstrom, C.E, Holmes, G.L

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Seizure-Induced Changes in Place Cell Physiology: Relationship to Spatial Memory von Liu, Xianzeng, Muller, Robert U, Huang, Li-Tung, Kubie, John L, Rotenberg, Alexander, Rivard, Bruno, Cilio, Maria Roberta, Holmes, Gregory L

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Timing of ketogenic diet initiation in an experimental epilepsy model von Su, Sharon W., Cilio, M.Roberta, Sogawa, Yoshimi, Silveira, Diosely, Holmes, Gregory L., Stafstrom, Carl E.

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The long-term use of felbamate in children with severe refractory epilepsy von Cilio, Maria Roberta, Kartashov, Alex I., Vigevano, Federico

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Childhood demyelinating diseases with a prolonged remitting course and their relation to Schilder’s disease: report of two cases von LEUZZI, VINCENZO, LYON, GILLES, CILIO, MARIA ROBERTA, PEDESPAN, JEAN MICHEL, FONTAN, DANIEL, CHATEIL, JEAN-FRANÇOIS, VITAL, ANNE

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Timing of cognitive deficits following neonatal seizures: relationship to histological changes in the hippocampus von Sogawa, Yoshimi, Monokoshi, Mitsuko, Silveira, Diosely C, Ho Cha, Byung, Roberta Cilio, Maria, McCabe, Bridget K, Liu, Xianzeng, Hu, Yingchun, Holmes, Gregory L

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Unusual cyclosporin related neurological complications in recipients of liver transplants von Cilio, M R, Danhaive, O, Gadisseux, J F, Otte, J B, Sokal, E M

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MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement von Brancati, Francesco, Iannicelli, Miriam, Travaglini, Lorena, Mazzotta, Annalisa, Bertini, Enrico, Boltshauser, Eugen, D'Arrigo, Stefano, Emma, Francesco, Fazzi, Elisa, Gallizzi, Romina, Gentile, Mattia, Loncarevic, Damir, Mejaski-Bosnjak, Vlatka, Pantaleoni, Chiara, Rigoli, Luciana, Salpietro, Carmelo D, Signorini, Sabrina, Stringini, Gilda Rita, Verloes, Alain, Zabloka, Dominika, Dallapiccola, Bruno, Gleeson, Joseph G, Valente, Enza Maria

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Mendelian Diseases among Roman Jews: Implications for the Origins of Disease Alleles von Oddoux, Carole, Guillen-Navarro, Encarnacion, DiTivoli, Claudio, DiCave Maria Roberta Cilio, Elvira, Clayton, C. Mark, Nelson, Holly, Sarafoglou, Kyriakie, McCain, Nicole, Peretz, Hava, Seligsohn, Uri, Luzzatto, Lucio, Nafa, Khedouja, Nardi, Michael, Karpatkin, Margaret, Aksentijevich, Ivona, Kastner, Daniel, Axelrod, Felicia, Ostrer, Harry

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