A case of familial central precocious puberty caused by a novel mutation in the makorin RING finger protein 3 gene

Por Grandone, Anna, Cantelmi, Grazia, Cirillo, Grazia, Marzuillo, Pierluigi, Luongo, Caterina, Miraglia del Giudice, Emanuele, Perrone, Laura
Publicado no BMC Endocr Disord (2015)

Very early onset of autoimmune thyroiditis in a toddler with severe hypothyroidism presentation: a case report

Por Marzuillo, Pierluigi, Grandone, Anna, Perrotta, Silverio, Ruggiero, Laura, Capristo, Carlo, Luongo, Caterina, Miraglia del Giudice, Emanuele, Perrone, Laura
Publicado no Ital J Pediatr (2016)

Novel cAMP binding protein-BP (CREBBP) mutation in a girl with Rubinstein-Taybi syndrome, GH deficiency, Arnold Chiari malformation and pituitary hypoplasia

Por Marzuillo, Pierluigi, Grandone, Anna, Coppola, Ruggero, Cozzolino, Domenico, Festa, Adalgisa, Messa, Federica, Luongo, Caterina, del Giudice, Emanuele Miraglia, Perrone, Laura
Publicado em 2013

Long-term safety and efficacy of Omnitrope®, a somatropin biosimilar, in children requiring growth hormone treatment: Italian interim analysis of the PATRO Children study

Por Iughetti, Lorenzo, Tornese, Gianluca, Street, Maria Elisabeth, Napoli, Flavia, Giavoli, Claudia, Antoniazzi, Franco, Stagi, Stefano, Luongo, Caterina, Azzolini, Sara, Ragusa, Letizia, Bona, Gianni, Zecchino, Clara, Aversa, Tommaso, Persani, Luca, Guazzarotti, Laura, Zecchi, Emiliano, Pietropoli, Alberto, Zucchini, Stefano
Publicado no Ital J Pediatr (2016)