Fatty liver disease and hypertransaminasemia hiding the association of clinically silent Duchenne muscular dystrophy and hereditary fructose intolerance

Por Paolella, Giulia, Pisano, Pasquale, Albano, Raffaele, Cannaviello, Lucio, Mauro, Carolina, Esposito, Gabriella, Vajro, Pietro
Publicado em 2012

Protein network study of human AF4 reveals its central role in RNA Pol II-mediated transcription and in phosphorylation-dependent regulatory mechanisms

Por Esposito, Gabriella, Cevenini, Armando, Cuomo, Alessandro, de Falco, Francesca, Sabbatino, Dario, Pane, Fabrizio, Ruoppolo, Margherita, Salvatore, Francesco
Publicado em 2011

Human aldolase A natural mutants: relationship between flexibility of the C-terminal region and enzyme function.

Por Esposito, Gabriella, Vitagliano, Luigi, Costanzo, Paola, Borrelli, Loredana, Barone, Rita, Pavone, Lorenzo, Izzo, Paola, Zagari, Adriana, Salvatore, Francesco
Publicado em 2004

Photoletter to the editor: Lamellar ichthyosis and arthrogryposis in a premature neonate

Por De Leonibus, Chiara, Lembo, Claudio, Santantonio, Alfredo, Fioretti, Tiziana, Rojo, Silvana, Salvatore, Francesco, De Vivo, Massimiliano, Esposito, Gabriella, Giliberti, Paolo
Publicado no J Dermatol Case Rep (2015)

Genetic characterization of Italian patients with Bardet-Biedl syndrome and correlation to ocular, renal and audio-vestibular phenotype: identification of eleven novel pathogenic s...

Por Esposito, Gabriella, Testa, Francesco, Zacchia, Miriam, Crispo, Anna Alessia, Di Iorio, Valentina, Capolongo, Giovanna, Rinaldi, Luca, D’Antonio, Marcella, Fioretti, Tiziana, Iadicicco, Pasquale, Rossi, Settimio, Franzè, Annamaria, Marciano, Elio, Capasso, Giovanbattista, Simonelli, Francesca, Salvatore, Francesco
Publicado no BMC Med Genet (2017)