PubMed (OMIM) for id: 389434

Year	Number of Results
1954	1
1956	1
1963	1
1964	1
1970	1
1974	1
1977	1
2004	1
2005	1
2006	1
2008	2
2024	0

1

Molecular characterization of iodotyrosine dehalogenase deficiency in patients with hypothyroidism.

Afink G, Kulik W, Overmars H, de Randamie J, Veenboer T, van Cruchten A, Craen M, Ris-Stalpers C. Afink G, et al. J Clin Endocrinol Metab. 2008 Dec;93(12):4894-901. doi: 10.1210/jc.2008-0865. Epub 2008 Sep 2. J Clin Endocrinol Metab. 2008. PMID: 18765512

2

Mutations in the iodotyrosine deiodinase gene and hypothyroidism.

Moreno JC, Klootwijk W, van Toor H, Pinto G, D'Alessandro M, Lèger A, Goudie D, Polak M, Grüters A, Visser TJ. Moreno JC, et al. N Engl J Med. 2008 Apr 24;358(17):1811-8. doi: 10.1056/NEJMoa0706819. N Engl J Med. 2008. PMID: 18434651 Free article.

3

Iodotyrosine deiodinase is the first mammalian member of the NADH oxidase/flavin reductase superfamily.

Friedman JE, Watson JA Jr, Lam DW, Rokita SE. Friedman JE, et al. J Biol Chem. 2006 Feb 3;281(5):2812-9. doi: 10.1074/jbc.M510365200. Epub 2005 Nov 29. J Biol Chem. 2006. PMID: 16316988 Free article.

4

Iodotyrosine dehalogenase 1 (DEHAL1) is a transmembrane protein involved in the recycling of iodide close to the thyroglobulin iodination site.

Gnidehou S, Caillou B, Talbot M, Ohayon R, Kaniewski J, Noël-Hudson MS, Morand S, Agnangji D, Sezan A, Courtin F, Virion A, Dupuy C. Gnidehou S, et al. FASEB J. 2004 Oct;18(13):1574-6. doi: 10.1096/fj.04-2023fje. Epub 2004 Aug 2. FASEB J. 2004. PMID: 15289438

5

THYROIDAL DEIODINATION DEFECT IN THREE SISTERS WITH SIMPLE GOITER.

KUSAKABE T, MIYAKE T. KUSAKABE T, et al. J Clin Endocrinol Metab. 1964 May;24:456-9. doi: 10.1210/jcem-24-5-456. J Clin Endocrinol Metab. 1964. PMID: 14169503 No abstract available.

6

Defective deiodination of I-131-labeled L-diiodotyrosine in patients with simple goiter.

KUSAKABE T, MIYAKE T. KUSAKABE T, et al. J Clin Endocrinol Metab. 1963 Feb;23:132-9. doi: 10.1210/jcem-23-2-132. J Clin Endocrinol Metab. 1963. PMID: 13927578 No abstract available.

7

Sporadic non-endemic goitrous cretinism; hereditary transmission.

HUTCHISON JH, MCGIRR EM. HUTCHISON JH, et al. Lancet. 1956 Jun 30;270(6931):1035-7. doi: 10.1016/s0140-6736(56)90800-5. Lancet. 1956. PMID: 13333116 No abstract available.

8

Hypothyroidism as an inborn error of metabolism.

HUTCHISON JH, McGIRR EM. HUTCHISON JH, et al. J Clin Endocrinol Metab. 1954 Aug;14(8):869-86. doi: 10.1210/jcem-14-8-869. J Clin Endocrinol Metab. 1954. PMID: 13183981 No abstract available.

9

[Infantile hypothyroidism caused by iodotyrosine-dehalogenase deficiency. II. Results of iodine treatment in 5 cases (8 years of recession in 1 case].

Codaccioni JL, Pierron H, Rouault F, Aquaron R, Jaquet P. Codaccioni JL, et al. Ann Endocrinol (Paris). 1970 Nov-Dec;31(6):1174-82. Ann Endocrinol (Paris). 1970. PMID: 4994830 French. No abstract available.

10

[Thyroid hormonosynthesis disorders due to iodotyrosine-dehalogenase deficiency. Value of the D.I.T. test for the detection of heterozygotes].

Rochiccioli P, Dutau G. Rochiccioli P, et al. Arch Fr Pediatr. 1974 Jan;31(1):25-36. Arch Fr Pediatr. 1974. PMID: 4135480 Clinical Trial. French. No abstract available.

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