Ferrara AM - Search Results

1

Changes in thyroid status during perinatal development of MCT8-deficient male mice.

Ferrara AM, Liao XH, Gil-Ibáñez P, Marcinkowski T, Bernal J, Weiss RE, Dumitrescu AM, Refetoff S. Ferrara AM, et al. Endocrinology. 2013 Jul;154(7):2533-41. doi: 10.1210/en.2012-2031. Epub 2013 May 21. Endocrinology. 2013. PMID: 23696569 Free PMC article.

2

Homozygous thyroid hormone receptor β-gene mutations in resistance to thyroid hormone: three new cases and review of the literature.

Ferrara AM, Onigata K, Ercan O, Woodhead H, Weiss RE, Refetoff S. Ferrara AM, et al. J Clin Endocrinol Metab. 2012 Apr;97(4):1328-36. doi: 10.1210/jc.2011-2642. Epub 2012 Feb 8. J Clin Endocrinol Metab. 2012. PMID: 22319036 Free PMC article. Review.

3

Mct8-deficient mice have increased energy expenditure and reduced fat mass that is abrogated by normalization of serum T3 levels.

Di Cosmo C, Liao XH, Ye H, Ferrara AM, Weiss RE, Refetoff S, Dumitrescu AM. Di Cosmo C, et al. Among authors: ferrara am. Endocrinology. 2013 Dec;154(12):4885-95. doi: 10.1210/en.2013-1150. Epub 2013 Sep 12. Endocrinology. 2013. PMID: 24029243 Free PMC article.

4

Placenta passage of the thyroid hormone analog DITPA to male wild-type and Mct8-deficient mice.

Ferrara AM, Liao XH, Gil-Ibáñez P, Bernal J, Weiss RE, Dumitrescu AM, Refetoff S. Ferrara AM, et al. Endocrinology. 2014 Oct;155(10):4088-93. doi: 10.1210/en.2014-1085. Epub 2014 Jul 22. Endocrinology. 2014. PMID: 25051435 Free PMC article.

5

A novel mechanism of inherited TBG deficiency: mutation in a liver-specific enhancer.

Ferrara AM, Pappa T, Fu J, Brown CD, Peterson A, Moeller LC, Wyne K, White KP, Pluzhnikov A, Trubetskoy V, Nobrega M, Weiss RE, Dumitrescu AM, Refetoff S. Ferrara AM, et al. J Clin Endocrinol Metab. 2015 Jan;100(1):E173-81. doi: 10.1210/jc.2014-3490. J Clin Endocrinol Metab. 2015. PMID: 25361180 Free PMC article.

6

The Thyroid Hormone Analog DITPA Ameliorates Metabolic Parameters of Male Mice With Mct8 Deficiency.

Ferrara AM, Liao XH, Ye H, Weiss RE, Dumitrescu AM, Refetoff S. Ferrara AM, et al. Endocrinology. 2015 Nov;156(11):3889-94. doi: 10.1210/en.2015-1234. Epub 2015 Aug 31. Endocrinology. 2015. PMID: 26322373 Free PMC article.

7

Coexistence of THRB and TBG gene mutations in a Turkish family.

Ferrara AM, Cakir M, Henry PH, Refetoff S. Ferrara AM, et al. J Clin Endocrinol Metab. 2013 Jun;98(6):E1148-51. doi: 10.1210/jc.2013-1413. Epub 2013 Apr 30. J Clin Endocrinol Metab. 2013. PMID: 23633200 Free PMC article.

8

A novel mutation in the Albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of Bangladeshi extraction.

Greenberg SM, Ferrara AM, Nicholas ES, Dumitrescu AM, Cody V, Weiss RE, Refetoff S. Greenberg SM, et al. Among authors: ferrara am. Thyroid. 2014 Jun;24(6):945-50. doi: 10.1089/thy.2013.0540. Epub 2014 Mar 21. Thyroid. 2014. PMID: 24494774 Free PMC article.

9

Inherited defects of thyroxine-binding proteins.

Pappa T, Ferrara AM, Refetoff S. Pappa T, et al. Among authors: ferrara am. Best Pract Res Clin Endocrinol Metab. 2015 Oct;29(5):735-47. doi: 10.1016/j.beem.2015.09.002. Epub 2015 Sep 30. Best Pract Res Clin Endocrinol Metab. 2015. PMID: 26522458 Free PMC article. Review.

10

A somatic gain-of-function mutation in the thyrotropin receptor gene producing a toxic adenoma in an infant.

Kohn B, Grasberger H, Lam LL, Ferrara AM, Refetoff S. Kohn B, et al. Among authors: ferrara am. Thyroid. 2009 Feb;19(2):187-91. doi: 10.1089/thy.2008.0302. Thyroid. 2009. PMID: 19191749 Free PMC article.

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