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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. Among authors: pappa t. 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.
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.
Resistance to Thyroid Hormone Beta: A Focused Review.
Pappa T, Refetoff S. Pappa T, et al. Front Endocrinol (Lausanne). 2021 Mar 31;12:656551. doi: 10.3389/fendo.2021.656551. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 33868182 Free PMC article. Review.
Evidence of primary aldosteronism in a predominantly female cohort of normotensive individuals: a very high odds ratio for progression into arterial hypertension.
Markou A, Pappa T, Kaltsas G, Gouli A, Mitsakis K, Tsounas P, Prevoli A, Tsiavos V, Papanastasiou L, Zografos G, Chrousos GP, Piaditis GP. Markou A, et al. Among authors: pappa t. J Clin Endocrinol Metab. 2013 Apr;98(4):1409-16. doi: 10.1210/jc.2012-3353. Epub 2013 Mar 7. J Clin Endocrinol Metab. 2013. PMID: 23471976 Clinical Trial.
60 results