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Divergent phenotype of two siblings human leukocyte antigen identical, affected by nonclassical and classical congenital adrenal hyperplasia caused by 21-hydroxylase deficiency.
Porzio O, Cunsolo V, Malaponti M, De Nisco E, Acquafredda A, Cavallo L, Andreani M, Giardina E, Testi M, Cappa M, Federici G. Porzio O, et al. Among authors: cavallo l. J Clin Endocrinol Metab. 2006 Nov;91(11):4510-3. doi: 10.1210/jc.2006-0779. Epub 2006 Aug 15. J Clin Endocrinol Metab. 2006. PMID: 16912133
[Constitutional delay of growth and puberty].
Cavallo L, Acquafredda A, Zecchino C, Delvecchio M. Cavallo L, et al. Minerva Pediatr. 2001 Oct;53(5):423-5. Minerva Pediatr. 2001. PMID: 11668263 Italian. No abstract available.
Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure.
Di Pasquale E, Rossetti R, Marozzi A, Bodega B, Borgato S, Cavallo L, Einaudi S, Radetti G, Russo G, Sacco M, Wasniewska M, Cole T, Beck-Peccoz P, Nelson LM, Persani L. Di Pasquale E, et al. Among authors: cavallo l. J Clin Endocrinol Metab. 2006 May;91(5):1976-9. doi: 10.1210/jc.2005-2650. Epub 2006 Feb 7. J Clin Endocrinol Metab. 2006. PMID: 16464940
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. Among authors: cavallo l. 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
814 results