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Accuracy of fine needle aspiration biopsy of thyroid nodules in detecting malignancy in childhood: comparison with conventional clinical, laboratory, and imaging approaches.
Corrias A, Einaudi S, Chiorboli E, Weber G, Crinò A, Andreo M, Cesaretti G, de Sanctis L, Messina MF, Segni M, Cicchetti M, Vigone M, Pasquino AM, Spera S, de Luca F, Mussa GC, Bona G. Corrias A, et al. Among authors: de sanctis l, de luca f. J Clin Endocrinol Metab. 2001 Oct;86(10):4644-8. doi: 10.1210/jcem.86.10.7950. J Clin Endocrinol Metab. 2001. PMID: 11600519
Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism.
De Sanctis L, Romagnolo D, Olivero M, Buzi F, Maghnie M, Scirè G, Crino A, Baroncelli GI, Salerno M, Di Maio S, Cappa M, Grosso S, Rigon F, Lala R, De Sanctis C, Dianzani I. De Sanctis L, et al. Among authors: de sanctis c. Pediatr Res. 2003 May;53(5):749-55. doi: 10.1203/01.PDR.0000059752.07086.A2. Epub 2003 Mar 5. Pediatr Res. 2003. PMID: 12621129
McCune-Albright syndrome: persistence of autonomous ovarian hyperfunction during adolescence and early adult age.
Matarazzo P, Lala R, Andreo M, Einaudi S, Altare F, Viora E, Buzi F, De Luca F, De Sanctis V, Rigon F, Wasniewska M, de Sanctis L, de Sanctis C; Study Group for Gs alpha Protein Related Diseases of the Italian Society for Pediatric Endocrinology and Diabetes. Matarazzo P, et al. Among authors: de sanctis c, de sanctis l, de luca f, de sanctis v. J Pediatr Endocrinol Metab. 2006 May;19 Suppl 2:607-17. doi: 10.1515/jpem.2006.19.s2.607. J Pediatr Endocrinol Metab. 2006. PMID: 16789624
GH secretion in a cohort of children with pseudohypoparathyroidism type Ia.
de Sanctis L, Bellone J, Salerno M, Faleschini E, Caruso-Nicoletti M, Cicchetti M, Concolino D, Balsamo A, Buzi F, Ghizzoni L, de Sanctis C. de Sanctis L, et al. Among authors: de sanctis c. J Endocrinol Invest. 2007 Feb;30(2):97-103. doi: 10.1007/BF03347406. J Endocrinol Invest. 2007. PMID: 17392598
214 results