These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
7. Genetics and phenomics of Pendred syndrome. Bizhanova A; Kopp P Mol Cell Endocrinol; 2010 Jun; 322(1-2):83-90. PubMed ID: 20298745 [TBL] [Abstract][Full Text] [Related]
8. Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome. Taylor JP; Metcalfe RA; Watson PF; Weetman AP; Trembath RC J Clin Endocrinol Metab; 2002 Apr; 87(4):1778-84. PubMed ID: 11932316 [TBL] [Abstract][Full Text] [Related]
9. [The diagnosis of the Pendred syndrome in children by the perchlorate discharge test with 123I (author's transl)]. Gross M; Hahn K; Biesalski HK HNO; 1981 Mar; 29(3):95-7. PubMed ID: 7216849 [TBL] [Abstract][Full Text] [Related]
10. Clinical and molecular characteristics of Pendred syndrome. Kopp P; Bizhanova A Ann Endocrinol (Paris); 2011 Apr; 72(2):88-94. PubMed ID: 21511235 [TBL] [Abstract][Full Text] [Related]
11. [123I-scintigraphy and perchlorate depletion test in the diagnosis of congenital hypothyroidism]. Meller J; Zappel H; Conrad M; Roth C; Emrich D; Becker W Nuklearmedizin; 1998 Jan; 37(1):7-11. PubMed ID: 9467163 [TBL] [Abstract][Full Text] [Related]
13. [Euthyroid goiter with and without functional autonomy in the euthyroid phase: a comparison]. Hillenhinrichs H; Emrich D Nuklearmedizin; 1998 May; 37(3):95-100. PubMed ID: 9604229 [TBL] [Abstract][Full Text] [Related]
14. Analysis of the SLC26A4 gene in patients with Pendred syndrome in Taiwan. Lai CC; Chiu CY; Shiao AS; Tso YC; Wu YC; Tu TY; Jap TS Metabolism; 2007 Sep; 56(9):1279-84. PubMed ID: 17697873 [TBL] [Abstract][Full Text] [Related]
15. [Global 99mTc uptake in the differential diagnosis of a normal thyroid,goiter with euthyroidism and thyroid autonomy in an area of iodine deficiency]. Kreisig T; Pickardt CR; Horn K; Bechtner G; Vaitl C; Kirsch CM; Knesewitsch P Nuklearmedizin; 1990 Jun; 29(3):113-9. PubMed ID: 2168038 [TBL] [Abstract][Full Text] [Related]
16. Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutation. Masmoudi S; Charfedine I; Hmani M; Grati M; Ghorbel AM; Elgaied-Boulila A; Drira M; Hardelin JP; Ayadi H Am J Med Genet; 2000 Jan; 90(1):38-44. PubMed ID: 10602116 [TBL] [Abstract][Full Text] [Related]