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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. Among authors: weber 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.
X-linked hypophosphatemic rickets: an Italian experts' opinion survey.
Emma F, Cappa M, Antoniazzi F, Bianchi ML, Chiodini I, Eller Vainicher C, Di Iorgi N, Maghnie M, Cassio A, Balsamo A, Baronio F, de Sanctis L, Tessaris D, Baroncelli GI, Mora S, Brandi ML, Weber G, D'Ausilio A, Lanati EP. Emma F, et al. Among authors: weber g. Ital J Pediatr. 2019 May 31;45(1):67. doi: 10.1186/s13052-019-0654-6. Ital J Pediatr. 2019. PMID: 31151476 Free PMC article.
Linear growth and puberty in childhood obesity: what is new?
Giglione E, Lapolla R, Cianfarani S, Faienza MF, Fintini D, Weber G, Delvecchio M, Valerio G. Giglione E, et al. Among authors: weber g. Minerva Pediatr (Torino). 2021 Dec;73(6):563-571. doi: 10.23736/S2724-5276.21.06543-5. Epub 2021 Jul 26. Minerva Pediatr (Torino). 2021. PMID: 34309346 Review.
Serum thyrotropin concentration in children with isolated thyroid nodules.
Mussa A, Salerno MC, Bona G, Wasniewska M, Segni M, Cassio A, Vigone MC, Gastaldi R, Iughetti L, Santanera A, Capalbo D, Matarazzo P, De Luca F, Weber G, Corrias A. Mussa A, et al. Among authors: weber g. J Pediatr. 2013 Nov;163(5):1465-70. doi: 10.1016/j.jpeds.2013.07.003. Epub 2013 Aug 22. J Pediatr. 2013. PMID: 23972643 Free article.
Thyroid nodules and cancer in children and adolescents affected by autoimmune thyroiditis.
Corrias A, Cassio A, Weber G, Mussa A, Wasniewska M, Rapa A, Gastaldi R, Einaudi S, Baronio F, Vigone MC, Messina MF, Bal M, Bona G, de Sanctis C; Study Group for Thyroid Diseases of Italian Society for Pediatric Endocrinology and Diabetology (SIEDP/ISPED). Corrias A, et al. Among authors: weber g. Arch Pediatr Adolesc Med. 2008 Jun;162(6):526-31. doi: 10.1001/archpedi.162.6.526. Arch Pediatr Adolesc Med. 2008. PMID: 18524742
Thyroid function in patients with Prader-Willi syndrome: an Italian multicenter study of 339 patients.
Iughetti L, Vivi G, Balsamo A, Corrias A, Crinò A, Delvecchio M, Gargantini L, Greggio NA, Grugni G, Hladnik U, Pilotta A, Ragusa L, Salvatoni A, Wasniewska M, Weber G, Predieri B. Iughetti L, et al. Among authors: weber g. J Pediatr Endocrinol Metab. 2019 Feb 25;32(2):159-165. doi: 10.1515/jpem-2018-0388. J Pediatr Endocrinol Metab. 2019. PMID: 30703060
Clinical presentation of McCune-Albright syndrome in males.
Wasniewska M, Matarazzo P, Weber G, Russo G, Zampolli M, Salzano G, Zirilli G, Bertelloni S; Italian Study Group for Alterations of Gs alpha Protein Function. Wasniewska M, et al. Among authors: weber g. J Pediatr Endocrinol Metab. 2006 May;19 Suppl 2:619-22. doi: 10.1515/jpem.2006.19.s2.619. J Pediatr Endocrinol Metab. 2006. PMID: 16789625
2,573 results