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Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation.
Colombo C, Delvecchio M, Zecchino C, Faienza MF, Cavallo L, Barbetti F; Early Onset Diabetes Study Group of the Italian Society of Paediatric Endocrinology and Diabetology. Colombo C, et al. Among authors: faienza mf. Diabetologia. 2005 Nov;48(11):2439-41. doi: 10.1007/s00125-005-1958-1. Epub 2005 Oct 5. Diabetologia. 2005. PMID: 16205880 No abstract available.
Osteoclastogenesis in children with 21-hydroxylase deficiency on long-term glucocorticoid therapy: the role of receptor activator of nuclear factor-kappaB ligand/osteoprotegerin imbalance.
Faienza MF, Brunetti G, Colucci S, Piacente L, Ciccarelli M, Giordani L, Del Vecchio GC, D'Amore M, Albanese L, Cavallo L, Grano M. Faienza MF, et al. J Clin Endocrinol Metab. 2009 Jul;94(7):2269-76. doi: 10.1210/jc.2008-2446. Epub 2009 Apr 28. J Clin Endocrinol Metab. 2009. PMID: 19401376
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence.
Bertelloni S, Balsamo A, Giordani L, Fischetto R, Russo G, Delvecchio M, Gennari M, Nicoletti A, Maggio MC, Concolino D, Cavallo L, Cicognani A, Chiumello G, Hiort O, Baroncelli GI, Faienza MF. Bertelloni S, et al. Among authors: faienza mf. J Endocrinol Invest. 2009 Sep;32(8):666-70. doi: 10.1007/BF03345738. Epub 2009 May 12. J Endocrinol Invest. 2009. PMID: 19498320
179 results