Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Costanza Frassinetti"'
Autor:
Michele Ghezzi, Costanza Frassinetti, Erika Calandra, Giovanna Giorgiani, Francesco Locatelli, M. Maghnie, F. De Terlizzi, Flavia Napoli, Andrea Secco, Annalisa Calcagno, N. di Iorgi
Publikováno v:
Journal of Endocrinological Investigation. 33:478-482
Background: Bone marrow transplantation (BMT) is associated with bone morbidity. We investigated bone status with quantitative ultrasound (QUS) in pediatric patients with hematological diseases prior to and up to 3 yr following BMT. Methods: Phalange
Autor:
Mohamad Maghnie, Sandro Loche, Costanza Frassinetti, Natascia Di Iorgi, Stefano Parodi, Maria Rosaria Casini, Flavia Napoli, Michele Ghezzi, Renata Lorini, Erika Calandra, Andrea Secco
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 94:4251-4257
Few studies have addressed the diagnostic role of the glucagon test in children with suspected GH deficiency (GHD).The objective of the study was to investigate the diagnostic value of the glucagon test as an alternative test to insulin tolerance tes
Autor:
Costanza Frassinetti, Flavia Napoli, Michele Ghezzi, Mohamad Maghnie, Natascia Di Iorgi, Anna Elsa Maria Allegri, Andrea Secco, Stefano Parodi, Linda Ambrosini, Erika Calandra, Roberto Gastaldi, Sandro Loche, Annalisa Calcagno
Publikováno v:
The Journal of clinical endocrinology and metabolism. 95(5)
The accuracy of the glucagon test in the diagnosis of central adrenal insufficiency in young children has not yet been definitively established.The aim of this study was to investigate the diagnostic accuracy of the glucagon test as an alternative to
Autor:
Michele Ghezzi, Yvonne Leitner, Annalisa Calcagno, Costanza Frassinetti, Flavia Napoli, Nadia Fratangeli, Monica Benassai, Andrea Secco, Natascia Di Iorgi, Renata Lorini, Roberto Gastaldi, Stefano Parodi, Giorgio Radetti, Erika Calandra, Mohamad Maghnie
Publikováno v:
The Journal of clinical endocrinology and metabolism. 94(11)
The 2007 Consensus Statement suggested a peak GH cutoff to insulin tolerance test (ITT) of less than 6 microg/liter in the diagnosis of permanent GH deficiency (GHD) in young adults with childhood-onset GHD (COGHD), although further validation was re