Radovick S - Search Results

1

Gangat M, Radovick S. Gangat M, et al. Among authors: radovick s. Endocrinol Metab Clin North Am. 2017 Jun;46(2):247-257. doi: 10.1016/j.ecl.2017.01.003. Epub 2017 Feb 22. Endocrinol Metab Clin North Am. 2017. PMID: 28476222 Review.

2

Precocious puberty.

Gangat M, Radovick S. Gangat M, et al. Among authors: radovick s. Minerva Pediatr. 2020 Dec;72(6):491-500. doi: 10.23736/S0026-4946.20.05970-8. Epub 2020 Aug 4. Minerva Pediatr. 2020. PMID: 32748611 Review.

3

Evidence That the Etiology of Congenital Hypopituitarism Has a Major Genetic Component but Is Infrequently Monogenic.

Jee YH, Gangat M, Yeliosof O, Temnycky AG, Vanapruks S, Whalen P, Gourgari E, Bleach C, Yu CH, Marshall I, Yanovski JA, Link K, Ten S, Baron J, Radovick S. Jee YH, et al. Among authors: radovick s. Front Genet. 2021 Aug 11;12:697549. doi: 10.3389/fgene.2021.697549. eCollection 2021. Front Genet. 2021. PMID: 34456972 Free PMC article.

4

Novel mutations associated with combined pituitary hormone deficiency.

Romero CJ, Pine-Twaddell E, Radovick S. Romero CJ, et al. Among authors: radovick s. J Mol Endocrinol. 2011 Jun 9;46(3):R93-R102. doi: 10.1530/JME-10-0133. Print 2011 Jun. J Mol Endocrinol. 2011. PMID: 21447626 Review.

5

A novel OTX2 mutation in a patient with combined pituitary hormone deficiency, pituitary malformation, and an underdeveloped left optic nerve.

Gorbenko Del Blanco D, Romero CJ, Diaczok D, de Graaff LC, Radovick S, Hokken-Koelega AC. Gorbenko Del Blanco D, et al. Among authors: radovick s. Eur J Endocrinol. 2012 Sep;167(3):441-52. doi: 10.1530/EJE-12-0333. Epub 2012 Jun 19. Eur J Endocrinol. 2012. PMID: 22715480

6

A novel dominant negative mutation of OTX2 associated with combined pituitary hormone deficiency.

Diaczok D, Romero C, Zunich J, Marshall I, Radovick S. Diaczok D, et al. Among authors: radovick s. J Clin Endocrinol Metab. 2008 Nov;93(11):4351-9. doi: 10.1210/jc.2008-1189. Epub 2008 Aug 26. J Clin Endocrinol Metab. 2008. PMID: 18728160 Free PMC article.

7

The role of CBP/p300 interactions and Pit-1 dimerization in the pathophysiological mechanism of combined pituitary hormone deficiency.

Cohen RN, Brue T, Naik K, Houlihan CA, Wondisford FE, Radovick S. Cohen RN, et al. Among authors: radovick s. J Clin Endocrinol Metab. 2006 Jan;91(1):239-47. doi: 10.1210/jc.2005-1211. Epub 2005 Nov 1. J Clin Endocrinol Metab. 2006. PMID: 16263824

8

The molecular basis of hypopituitarism.

Romero CJ, Nesi-França S, Radovick S. Romero CJ, et al. Among authors: radovick s. Trends Endocrinol Metab. 2009 Dec;20(10):506-16. doi: 10.1016/j.tem.2009.06.005. Epub 2009 Oct 23. Trends Endocrinol Metab. 2009. PMID: 19854060 Free PMC article. Review.

9

Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia.

Raivio T, Avbelj M, McCabe MJ, Romero CJ, Dwyer AA, Tommiska J, Sykiotis GP, Gregory LC, Diaczok D, Tziaferi V, Elting MW, Padidela R, Plummer L, Martin C, Feng B, Zhang C, Zhou QY, Chen H, Mohammadi M, Quinton R, Sidis Y, Radovick S, Dattani MT, Pitteloud N. Raivio T, et al. Among authors: radovick s. J Clin Endocrinol Metab. 2012 Apr;97(4):E694-9. doi: 10.1210/jc.2011-2938. Epub 2012 Feb 8. J Clin Endocrinol Metab. 2012. PMID: 22319038 Free PMC article. Clinical Trial.

10

Molecular basis of combined pituitary hormone deficiencies.

Cohen LE, Radovick S. Cohen LE, et al. Among authors: radovick s. Endocr Rev. 2002 Aug;23(4):431-42. doi: 10.1210/er.2001-0030. Endocr Rev. 2002. PMID: 12202459 Review.

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