Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Rosanna Lia"'
Autor:
Stefano Passanisi, Giuseppina Salzano, Monica Aloe, Bruno Bombaci, Felice Citriniti, Fiorella De Berardinis, Rosaria De Marco, Nicola Lazzaro, Maria C. Lia, Rosanna Lia, Francesco Mammì, Filomena A. Stamati, Rosanna M. R. Toscano, Claudia Ventrici, Dario Iafusco, Fortunato Lombardo
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-8 (2022)
Abstract Background Although type 1 diabetes (T1D) represents one of the most common chronic diseases in pediatric age, few studies on the epidemiology of T1D exist globally and the exact prevalence and incidence rates of the disease are unknown. In
Externí odkaz:
https://doaj.org/article/5360fad9caea40a091b831d349af6457
Autor:
Malgorzata Wasniewska, Maria Chiara Pellegrin, Rita Fischetto, Francesca Macchi, Antonella Lonero, Sara Osimani, A. Crinò, Adriana Franzese, Sarah Bocchini, Gilda Cassano, Luana Nosetti, Annamaria Perri, Giuseppa Patti, Maria Rosaria Licenziati, Michele Sacco, Stefano Stagi, Alessandro Salvatoni, G. Trifirò, Rosanna Lia, Simona Filomena Madeo, Irene Rutigliano, Lorenzo Iughetti, Paola Giordano, Danilo Fintini, Gianluca Tornese, Alessio Convertino, Patrizia Matarazzo, Graziano Grugni, S. Ferraris, Emanuela Scarano, Domenico Corica, Valentina Fattorusso, Viviana Valeria Palmieri, Roberta Pajno, L. Ragusa, Maurizio Delvecchio
Pediatric patients with Prader-Willi syndrome (PWS) can be treated with recombinant human GH (rhGH). These patients are highly sensitive to rhGH and the standard doses suggested by the international guidelines often result in IGF-1 above the normal r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7a8e3ec15413420522c8d0ddc251830
http://hdl.handle.net/11588/770080
http://hdl.handle.net/11588/770080
Autor:
Giovanni Melioli, Maja Di Rocco, S. Paci, Laura Barbagallo, Sebastiano Barco, Marcello Giovannini, Giuliana Cangemi, Giacomo Biasucci, Rosanna Lia
Publikováno v:
Scandinavian journal of clinical and laboratory investigation. 72(1)
Classical galactosemia is a rare but very severe disease characterized by a deficiency of the galactose-1-phosphate uridyltransferase enzyme. The confirmed galactosemic patients are treated with a galactose-restricted diet. Nevertheless, metabolites