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.
133 related articles for article (PubMed ID: 5677816)
1. [Discussion of Pendred's syndrome. Apropos of a goiter caused by a disorder of hormonogenesis and associated with hereditary perception deafness]. Bouchard R; Guedeney J; Mazet P; Castaing N Arch Fr Pediatr; 1968 Apr; 25(4):453-63. PubMed ID: 5677816 [No Abstract] [Full Text] [Related]
2. [Pendred's syndrome: a clinical and biochemical study of abnormal thyroid hormone synthesis associated with congenital deaf-mutism]. de Medeiros-Netto GA; Nicolau W; Cintra AB Rev Paul Med; 1969 Feb; 74(2):53-74. PubMed ID: 4190511 [No Abstract] [Full Text] [Related]
3. [Strumectomy in the syndrome of congenital deafness and goiter (Pendred's syndrome)]. Bielicki F; Bielicka E; Noczyński L; Zagrobelny Z; Zukowski W Pol Przegl Chir; 1970 Dec; 42(12):1814-7. PubMed ID: 5497325 [No Abstract] [Full Text] [Related]
4. [Pendred's syndrome. Apropos of 2 familial cases]. van de Velde-Staquet MF; Gnamey DK; Delattre B; Queva B; Desbonnets P; Farriaux JP Lille Med; 1972 Oct; 17(9):1249-55. PubMed ID: 4657636 [No Abstract] [Full Text] [Related]
5. [Combined goiter and deafness as a hereditary condition (Pendred's syndrome)]. Sundsfjord JA; Schjoth A; Odegaard AE; Harbitz HF Tidsskr Nor Laegeforen; 1968 Jan; 88(1):19-23. PubMed ID: 4174251 [No Abstract] [Full Text] [Related]
8. Congenital deafness and goiter (Pendred's syndrome). Bilginturan N Turk J Pediatr; 1966 Oct; 8(4):216-21. PubMed ID: 5978649 [No Abstract] [Full Text] [Related]
9. Pendred's syndrome. Dogra KN; Thaman OP Indian Pediatr; 1966 Dec; 3(12):429-34. PubMed ID: 5980166 [No Abstract] [Full Text] [Related]
10. Pendred's syndrome and genetic defects in thyroid hormone synthesis. Kopp P Rev Endocr Metab Disord; 2000 Jan; 1(1-2):109-21. PubMed ID: 11704986 [No Abstract] [Full Text] [Related]
11. Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity. Blons H; Feldmann D; Duval V; Messaz O; Denoyelle F; Loundon N; Sergout-Allaoui A; Houang M; Duriez F; Lacombe D; Delobel B; Leman J; Catros H; Journel H; Drouin-Garraud V; Obstoy MF; Toutain A; Oden S; Toublanc JE; Couderc R; Petit C; Garabédian EN; Marlin S Clin Genet; 2004 Oct; 66(4):333-40. PubMed ID: 15355436 [TBL] [Abstract][Full Text] [Related]
12. [On 3 cases of familial goiter due to probable congenital defect of hormonogenesis]. Torino G; Esposito V Pediatria (Napoli); 1972; 80(4):388-97. PubMed ID: 4646632 [No Abstract] [Full Text] [Related]
13. [Pendred's syndrome and goiter endemia]. Ferraris GM; Zoppetti G; Bidone G; Costa A Folia Endocrinol; 1966 Jun; 19(3):295-312. PubMed ID: 6012940 [No Abstract] [Full Text] [Related]