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Frequent TSH receptor genetic alterations with variable signaling impairment in a large series of children with nonautoimmune isolated hyperthyrotropinemia.
Calebiro D, Gelmini G, Cordella D, Bonomi M, Winkler F, Biebermann H, de Marco A, Marelli F, Libri DV, Antonica F, Vigone MC, Cappa M, Mian C, Sartorio A, Beck-Peccoz P, Radetti G, Weber G, Persani L. Calebiro D, et al. Among authors: cappa m. J Clin Endocrinol Metab. 2012 Jan;97(1):E156-60. doi: 10.1210/jc.2011-1938. Epub 2011 Nov 2. J Clin Endocrinol Metab. 2012. PMID: 22049173
Central precocious puberty: treatment with triptorelin 11.25 mg.
Chiocca E, Dati E, Baroncelli GI, Cassio A, Wasniewska M, Galluzzi F, Einaudi S, Cappa M, Russo G, Bertelloni S. Chiocca E, et al. Among authors: cappa m. ScientificWorldJournal. 2012;2012:583751. doi: 10.1100/2012/583751. Epub 2012 May 3. ScientificWorldJournal. 2012. PMID: 22645436 Free PMC article.
Congenital hypothyroidism due to defects of thyroid development and mild increase of TSH at screening: data from the Italian National Registry of infants with congenital hypothyroidism.
Olivieri A, Corbetta C, Weber G, Vigone MC, Fazzini C, Medda E; Italian Study Group for Congenital Hypothyroidism. Olivieri A, et al. J Clin Endocrinol Metab. 2013 Apr;98(4):1403-8. doi: 10.1210/jc.2012-3273. Epub 2013 Feb 26. J Clin Endocrinol Metab. 2013. PMID: 23443814
397 results