Similar articles for PMID: 20834201

Year	Number of Results
1907	1
1933	1
1980	1
1986	1
1999	2
2000	3
2001	1
2002	2
2003	1
2004	3
2005	1
2006	7
2007	7
2008	11
2009	4
2010	7
2011	19
2012	8
2013	8
2014	7
2015	4
2016	6
2017	4
2018	4
2019	7
2020	2
2021	8
2022	9
2023	3
2024	1

1

Absence of primary hypothyroidism and goiter in Slc26a4 (-/-) mice fed on a low iodine diet.

Calebiro D, Porazzi P, Bonomi M, Lisi S, Grindati A, De Nittis D, Fugazzola L, Marinò M, Bottà G, Persani L. Calebiro D, et al. J Endocrinol Invest. 2011 Sep;34(8):593-8. doi: 10.3275/7262. Epub 2010 Sep 9. J Endocrinol Invest. 2011. PMID: 20834201

2

Pendred syndrome.

Wémeau JL, Kopp P. Wémeau JL, et al. Best Pract Res Clin Endocrinol Metab. 2017 Mar;31(2):213-224. doi: 10.1016/j.beem.2017.04.011. Epub 2017 May 10. Best Pract Res Clin Endocrinol Metab. 2017. PMID: 28648509 Review.

3

Sgk1 sensitive pendrin expression in murine platelets.

Pelzl L, Fakhri H, Umbach AT, Gawaz M, Paulmichl M, Lang F. Pelzl L, et al. Cell Physiol Biochem. 2013;32(7):210-20. doi: 10.1159/000356640. Epub 2013 Dec 18. Cell Physiol Biochem. 2013. PMID: 24429827 Free article.

4

Mutations in the SLC26A4 (pendrin) gene in patients with sensorineural deafness and enlarged vestibular aqueduct.

Bogazzi F, Russo D, Raggi F, Ultimieri F, Berrettini S, Forli F, Grasso L, Ceccarelli C, Mariotti S, Pinchera A, Bartalena L, Martino E. Bogazzi F, et al. J Endocrinol Invest. 2004 May;27(5):430-5. doi: 10.1007/BF03345286. J Endocrinol Invest. 2004. PMID: 15279074

5

Clinical and molecular characteristics of Pendred syndrome.

Kopp P, Bizhanova A. Kopp P, et al. Ann Endocrinol (Paris). 2011 Apr;72(2):88-94. doi: 10.1016/j.ando.2011.03.010. Epub 2011 Apr 20. Ann Endocrinol (Paris). 2011. PMID: 21511235

6

Analysis of the thyroid phenotype in 42 patients with Pendred syndrome and nonsyndromic enlargement of the vestibular aqueduct.

Ladsous M, Vlaeminck-Guillem V, Dumur V, Vincent C, Dubrulle F, Dhaenens CM, Wémeau JL. Ladsous M, et al. Thyroid. 2014 Apr;24(4):639-48. doi: 10.1089/thy.2013.0164. Epub 2014 Jan 20. Thyroid. 2014. PMID: 24224479

7

Hereditary hearing loss with thyroid abnormalities.

Choi BY, Muskett J, King KA, Zalewski CK, Shawker T, Reynolds JC, Butman JA, Brewer CC, Stewart AK, Alper SL, Griffith AJ. Choi BY, et al. Adv Otorhinolaryngol. 2011;70:43-49. doi: 10.1159/000322469. Epub 2011 Feb 24. Adv Otorhinolaryngol. 2011. PMID: 21358184 Review.

8

Pendrin: the thyrocyte apical membrane iodide transporter?

Twyffels L, Massart C, Golstein PE, Raspe E, Van Sande J, Dumont JE, Beauwens R, Kruys V. Twyffels L, et al. Cell Physiol Biochem. 2011;28(3):491-6. doi: 10.1159/000335110. Epub 2011 Nov 18. Cell Physiol Biochem. 2011. PMID: 22116362 Free article. Review.

9

TSH regulates pendrin membrane abundance and enhances iodide efflux in thyroid cells.

Pesce L, Bizhanova A, Caraballo JC, Westphal W, Butti ML, Comellas A, Kopp P. Pesce L, et al. Endocrinology. 2012 Jan;153(1):512-21. doi: 10.1210/en.2011-1548. Epub 2011 Nov 22. Endocrinology. 2012. PMID: 22109890 Free PMC article.

10

Pendred syndrome in two Galician families: insights into clinical phenotypes through cellular, genetic, and molecular studies.

Palos F, García-Rendueles ME, Araujo-Vilar D, Obregon MJ, Calvo RM, Cameselle-Teijeiro J, Bravo SB, Perez-Guerra O, Loidi L, Czarnocka B, Alvarez P, Refetoff S, Dominguez-Gerpe L, Alvarez CV, Lado-Abeal J. Palos F, et al. J Clin Endocrinol Metab. 2008 Jan;93(1):267-77. doi: 10.1210/jc.2007-0539. Epub 2007 Oct 16. J Clin Endocrinol Metab. 2008. PMID: 17940114 Free PMC article.

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