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Pharmacogenomics of insulin-like growth factor-I generation during GH treatment in children with GH deficiency or Turner syndrome.
Stevens A, Clayton P, Tatò L, Yoo HW, Rodriguez-Arnao MD, Skorodok J, Ambler GR, Zignani M, Zieschang J, Della Corte G, Destenaves B, Champigneulle A, Raelson J, Chatelain P. Stevens A, et al. Among authors: tato l. Pharmacogenomics J. 2014 Feb;14(1):54-62. doi: 10.1038/tpj.2013.14. Epub 2013 Apr 9. Pharmacogenomics J. 2014. PMID: 23567489 Free PMC article. Clinical Trial.
A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome.
Clayton P, Chatelain P, Tatò L, Yoo HW, Ambler GR, Belgorosky A, Quinteiro S, Deal C, Stevens A, Raelson J, Croteau P, Destenaves B, Olivier C. Clayton P, et al. Among authors: tato l. Eur J Endocrinol. 2013 Jul 29;169(3):277-89. doi: 10.1530/EJE-13-0069. Print 2013 Sep. Eur J Endocrinol. 2013. PMID: 23761422 Free PMC article. Clinical Trial.
[Growth and renal function].
Antoniazzi F, Mengarda F, Lauriola S, Serra A, Zamboni G, Tatò L. Antoniazzi F, et al. Among authors: tato l. Pediatr Med Chir. 1997 Sep-Oct;19(5):341-7. Pediatr Med Chir. 1997. PMID: 9493225 Review. Italian.
Bone development during GH and GnRH analog treatment.
Antoniazzi F, Zamboni G, Bertoldo F, Lauriola S, Tatò L. Antoniazzi F, et al. Among authors: tato l. Eur J Endocrinol. 2004 Aug;151 Suppl 1:S47-54. doi: 10.1530/eje.0.151s047. Eur J Endocrinol. 2004. PMID: 15339244 Free article. Review.
185 results