Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2011 1
2012 3
2013 1
2014 5
2015 6
2016 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

16 results

Results by year

Filters applied: . Clear all
Page 1
Inherited defects of thyroxine-binding proteins.
Pappa T, Ferrara AM, Refetoff S. Pappa T, et al. 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.
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.
Long-term outcome of loss-of-function mutations in thyrotropin receptor gene.
Tenenbaum-Rakover Y, Almashanu S, Hess O, Admoni O, Hag-Dahood Mahameed A, Schwartz N, Allon-Shalev S, Bercovich D, Refetoff S. Tenenbaum-Rakover Y, et al. Thyroid. 2015 Mar;25(3):292-9. doi: 10.1089/thy.2014.0311. Epub 2015 Jan 28. Thyroid. 2015. PMID: 25557138 Free PMC article.
Diiodothyropropionic acid (DITPA) in the treatment of MCT8 deficiency.
Verge CF, Konrad D, Cohen M, Di Cosmo C, Dumitrescu AM, Marcinkowski T, Hameed S, Hamilton J, Weiss RE, Refetoff S. Verge CF, et al. J Clin Endocrinol Metab. 2012 Dec;97(12):4515-23. doi: 10.1210/jc.2012-2556. Epub 2012 Sep 19. J Clin Endocrinol Metab. 2012. PMID: 22993035 Free PMC article.
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.
The coexistence of a novel inactivating mutant thyrotropin receptor allele with two thyroid peroxidase mutations: a genotype-phenotype correlation.
Sriphrapradang C, Tenenbaum-Rakover Y, Weiss M, Barkoff MS, Admoni O, Kawthar D, Caltabiano G, Pardo L, Dumitrescu AM, Refetoff S. Sriphrapradang C, et al. J Clin Endocrinol Metab. 2011 Jun;96(6):E1001-6. doi: 10.1210/jc.2011-0127. Epub 2011 Apr 13. J Clin Endocrinol Metab. 2011. PMID: 21490078 Free PMC article.
16 results