Limbal Stem Cell Deficiency and Ocular Phenotype in Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome Caused by p63 Mutations von Di Iorio, Enzo, PhD, Kaye, Stephen B., MD, Ponzin, Diego, MD, Barbaro, Vanessa, PhD, Ferrari, Stefano, PhD, Böhm, Elisabetta, MD, Nardiello, Paola, PhD, Castaldo, Giuseppe, MD, PhD, McGrath, John A., MD, Willoughby, Colin E., MD

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First Diagnosis of Hemophilia B in a Nonagenarian von Bury, Loredana, Nardiello, Paola, Fierro, Tiziana, Zarrilli, Federica, Coppola, Antonio, Castaldo, Giuseppe, Gresele, Paolo

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Prenatal diagnosis of cystic fibrosis: an experience of 181 cases von Tomaiuolo, Rossella, Nardiello, Paola, Martinelli, Pasquale, Sacchetti, Lucia, Salvatore, Francesco, Castaldo, Giuseppe

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Phenotypic Heterogeneity in a Cystic Fibrosis Family and the “Pseudomonas Dilemma” von Salvatore, Donatello, Colangelo, Carmela, Nardiello, Paola, Castaldo, Giuseppe

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Haemophilia A: molecular insights von Castaldo, Giuseppe, D'Argenio, Valeria, Nardiello, Paola, Zarrilli, Federica, Sanna, Veronica, Rocino, Angiola, Coppola, Antonio, Di Minno, Giovanni, Salvatore, Francesco

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A novel de novo missense mutation in TP63 underlying germline mosaicism in AEC syndrome: Implications for recurrence risk and prenatal diagnosis von Barbaro, Vanessa, Nardiello, Paola, Castaldo, Giuseppe, Willoughby, Colin E., Ferrari, Stefano, Ponzin, Diego, Amato, Felice, Bonifazi, Ernesto, Parekh, Mohit, Calistri, Arianna, Parolin, Cristina, Di Iorio, Enzo

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Denaturing HPLC procedure for factor IX gene scanning von CASTALDO, Giuseppe, NARDIELLO, Paola, BELLITTI, Fabiana, ROCINO, Angiola, COPPOLA, Antonio, DI MINNO, Giovafini, SALVATORE, Francesco

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Haemophilia B: From Molecular Diagnosis to Gene Therapy von Castaldo, Giuseppe, Nardiello, Paola, Bellitti, Fabiana, Santamaria, Rita, Rocino, Angiola, Coppola, Antonio, Minno, Giovanni di, Salvatore, Francesco

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First Diagnosis of Hemophilia B in a Nonagenarian von Bury, Loredana, Nardiello, Paola, Fierro, Tiziana, Zarrilli, Federica, Coppola, Antonio, Castaldo, Giuseppe, Gresele, Paolo

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A novel de novo missense mutation in TP63 underlying germline mosaicism in AEC syndrome: Implications for recurrence risk and prenatal diagnosis von Barbaro, Vanessa, Nardiello, Paola, Castaldo, Giuseppe, Willoughby, Colin E., Ferrari, Stefano, Ponzin, Diego, Amato, Felice, Bonifazi, Ernesto, Parekh, Mohit, Calistri, Arianna, Parolin, Cristina, Di Iorio, Enzo

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The GAPS Programme at TNG von Basilicata, M, Giacobbe, P, Bonomo, A S, Scandariato, G, Brogi, M, Singh, V, A. Di Paola, Mancini, L, Sozzetti, A, Lanza, A F, Cubillos, P E, Damasso, M, Desidera, S, Biazzo, K, Bignamini, A, Borsa, F, Cabona, L, Carleo, I, Ghedina, A, Guilluy, G, Maggio, A, Mainella, G, Micela, G, Molinari, E, Molinaro, M, Nardiello, D, Pedani, M, Pino, L, Poretti, E, Southworth, J, Stangret, M, Turrini, D

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The GAPS Programme at TNG: LV. Multiple molecular species in the atmosphere of HAT-P-11 b and review of the HAT-P-11 planetary system von Basilicata, M., Giacobbe, P., Bonomo, A. S., Scandariato, G., Brogi, M., Singh, V., Di Paola, A., Mancini, L., Sozzetti, A., Lanza, A. F., Cubillos, P. E., Damasso, M., Desidera, S., Biazzo, K., Bignamini, A., Borsa, F., Cabona, L., Carleo, I., Ghedina, A., Guilluy, G., Maggio, A., Mainella, G., Micela, G., Molinari, E., Molinaro, M., Nardiello, D., Pedani, M., Pino, L., Poretti, E., Southworth, J., Stangret, M., Turrini, D.

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The GAPS Programme at TNG LV. Multiple molecular species in the atmosphere of HAT-P-11 b and review of the HAT-P-11 planetary system von Basilicata, M, Giacobbe, P, Bonomo, A S, Scandariato, G, Brogi, M, Singh, V, A Di Paola, Mancini, L, Sozzetti, A, Lanza, A F, Cubillos, P E, Damasso, M, Desidera, S, Biazzo, K, Bignamini, A, Borsa, F, Cabona, L, Carleo, I, Ghedina, A, Guilluy, G, Maggio, A, Mainella, G, Micela, G, Molinari, E, Molinaro, M, Nardiello, D, Pedani, M, Pino, L, Poretti, E, Southworth, J, Stangret, M, Turrini, D

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