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Page 1
Longitudinal neuropsychological profile in a patient with triple a syndrome.
Mazzone L, Postorino V, De Peppo L, Vassena L, Fatta L, Armando M, Scirè G, Cappa M, Vicari S. Mazzone L, et al. Among authors: scire g. Case Rep Pediatr. 2013;2013:604921. doi: 10.1155/2013/604921. Epub 2013 Apr 9. Case Rep Pediatr. 2013. PMID: 23691407 Free PMC article.
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: scire g. 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
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. Among authors: scire g. 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.
57 results