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Genetic and epigenetic alterations in the GNAS locus and clinical consequences in Pseudohypoparathyroidism: Italian common healthcare pathways adoption.
de Sanctis L, Giachero F, Mantovani G, Weber G, Salerno M, Baroncelli GI, Elli MF, Matarazzo P, Wasniewska M, Mazzanti L, Scirè G, Tessaris D; Study Group Endocrine diseases due to altered function of Gsα protein of the Italian Society of Pediatric Endocrinology and Diabetology (ISPED). de Sanctis L, et al. Ital J Pediatr. 2016 Nov 21;42(1):101. doi: 10.1186/s13052-016-0310-3. Ital J Pediatr. 2016. PMID: 27871293 Free PMC article.
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
217 results