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Page 1
Short stature homeoboxcontaining gene and idiopathic short stature.
Iughetti L, Appio P, Capone L, Madeo S, Predieri B, Balli F, Forabosco A. Iughetti L, et al. Among authors: forabosco a. Expert Rev Endocrinol Metab. 2009 May;4(3):241-250. doi: 10.1586/eem.09.5. Expert Rev Endocrinol Metab. 2009. PMID: 30743796
The SHOX region and its mutations.
Capone L, Iughetti L, Sabatini S, Bacciaglia A, Forabosco A. Capone L, et al. Among authors: forabosco a. J Endocrinol Invest. 2010 Jun;33(6 Suppl):11-4. J Endocrinol Invest. 2010. PMID: 21057179
Unexpected phenotype in a boy with trisomy of the SHOX gene.
Iughetti L, Capone L, Elsedfy H, Bertorelli R, Predieri B, Bruzzi P, Forabosco A, El Kholy M. Iughetti L, et al. Among authors: forabosco a. J Pediatr Endocrinol Metab. 2010 Jan-Feb;23(1-2):159-69. doi: 10.1515/jpem.2010.23.1-2.159. J Pediatr Endocrinol Metab. 2010. PMID: 20432819
SHOX gene in Leri-Weill syndrome and in idiopathic short stature.
Bernasconi S, Mariani S, Falcinelli C, Milioli S, Iughetti L, Forabosco A. Bernasconi S, et al. Among authors: forabosco a. J Endocrinol Invest. 2001 Oct;24(9):737-41. doi: 10.1007/BF03343919. J Endocrinol Invest. 2001. PMID: 11716161 Review. No abstract available.
SHOX point mutations and deletions in Leri-Weill dyschondrosteosis.
Falcinelli C, Iughetti L, Percesepe A, Calabrese G, Chiarelli F, Cisternino M, De Sanctis L, Pucarelli I, Radetti G, Wasniewska M, Weber G, Stuppia L, Bernasconi S, Forabosco A. Falcinelli C, et al. Among authors: forabosco a. J Med Genet. 2002 Jun;39(6):E33. doi: 10.1136/jmg.39.6.e33. J Med Genet. 2002. PMID: 12070265 Free PMC article. No abstract available.
179 results