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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

103 related articles for article (PubMed ID: 443737)

  • 1. [Quantitative aspects of iodine metabolism in one case of congenital iodotyrosine deiodinase defect (author's transl)].
    Savoie JC; Baulieu JL; Savoie F; Leger FA; Piette C; Sebaoun J
    Ann Endocrinol (Paris); 1979; 40(1):55-6. PubMed ID: 443737
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Thyroid iodine organification defects: a case with lack of thyroglobulin iodination and a case without any peroxidase activity.
    Pommier J; Tourniaire J; Rahmoun B; Déme D; Pallo D; Bornet H; Nunez J
    J Clin Endocrinol Metab; 1976 Feb; 42(2):319-29. PubMed ID: 1262432
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Iodotyrosine deiodinase defect identified via genome-wide approach.
    Burniat A; Pirson I; Vilain C; Kulik W; Afink G; Moreno-Reyes R; Corvilain B; Abramowicz M
    J Clin Endocrinol Metab; 2012 Jul; 97(7):E1276-83. PubMed ID: 22535972
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The test of overloading L-diiodotyrosine (DIT) in the screening of iodotyrosine dehalogenase deficiency.
    Codaccioni JL; Rinaldi JP; Bismuth J
    Acta Endocrinol (Copenh); 1978 Jan; 87(1):95-105. PubMed ID: 579538
    [No Abstract]   [Full Text] [Related]  

  • 5. Deficient thyroid peroxidase causing organification defect and goitrous hypothyroidism.
    Medeiros-Neto GA; Knobel M; Yamamoto K; Cavaliere H; Kallas W
    J Endocrinol Invest; 1979; 2(4):353-7. PubMed ID: 231615
    [No Abstract]   [Full Text] [Related]  

  • 6. A variant of iodotyrosine-dehalogenase deficiency.
    Ismail-Beigi F; Rahimifar M
    J Clin Endocrinol Metab; 1977 Mar; 44(3):499-506. PubMed ID: 838849
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Towards the pre-clinical diagnosis of hypothyroidism caused by iodotyrosine deiodinase (DEHAL1) defects.
    Iglesias A; García-Nimo L; Cocho de Juan JA; Moreno JC
    Best Pract Res Clin Endocrinol Metab; 2014 Mar; 28(2):151-9. PubMed ID: 24629858
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Congenital Hypothyroidism in Two Sudanese Families Harboring a Novel Iodotyrosine Deiodinase Mutation (IYD R279C).
    Shareef R; Furman A; Watanabe Y; Bruellman R; Abdullah MA; Dumitresu AM; Refetoff S; Bertolini A; Borsò M; Saba A; Zucchi R; Weiss RE
    Thyroid; 2023 Feb; 33(2):261-266. PubMed ID: 36633921
    [No Abstract]   [Full Text] [Related]  

  • 9. Genetics and phenomics of hypothyroidism and goiter due to iodotyrosine deiodinase (DEHAL1) gene mutations.
    Moreno JC; Visser TJ
    Mol Cell Endocrinol; 2010 Jun; 322(1-2):91-8. PubMed ID: 20298747
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    N Engl J Med; 2008 Apr; 358(17):1811-8. PubMed ID: 18434651
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Studies on mono- and diiodohistidine. II. Congenital goitrous hypothyroidism with thyroglobulin defect and iodohistidine-rich iodoalbumin production.
    Savoie JC; Massin JP; Savoie F
    J Clin Invest; 1973 Jan; 52(1):116-25. PubMed ID: 4629905
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Iodotyrosines Are Biomarkers for Preclinical Stages of Iodine-Deficient Hypothyroidism in
    González-Guerrero C; Borsò M; Alikhani P; Alcaina Y; Salas-Lucia F; Liao XH; García-Giménez J; Bertolini A; Martin D; Moratilla A; Mora R; Buño-Soto A; Mani AR; Bernal J; Saba A; de Miguel MP; Refetoff S; Zucchi R; Moreno JC
    Thyroid; 2023 Jun; 33(6):752-761. PubMed ID: 36879468
    [No Abstract]   [Full Text] [Related]  

  • 13. Would I-123 di-iodotyrosine provide a harmless deiodination test? Concise communication.
    Aurengo A; Savoie F; Leger AF; Savoie JC
    J Nucl Med; 1983 Dec; 24(12):1143-8. PubMed ID: 6315903
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evolution of hypothyroidism in familial goitre due to deiodinase deficiency: report of a family and review of the literature.
    Hirsch HJ; Shilo S; Spitz IM
    Postgrad Med J; 1986 Jun; 62(728):477-80. PubMed ID: 3774680
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Defective thyroidal iodine concentration in protein-calorie malnutrition.
    Gaitan JE; Mayoral LG; Gaitan E
    J Clin Endocrinol Metab; 1983 Aug; 57(2):327-33. PubMed ID: 6408112
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Goitrous hypothyroidism due to iodide-trapping defect.
    Saito K; Yamamoto K; Yoshida S; Manabe S; Suzuki M; Takai T; Saito T; Kuzuya T; Moriyama S
    J Clin Endocrinol Metab; 1981 Dec; 53(6):1267-72. PubMed ID: 6271803
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Congenital goitre due to "thyroid peroxidase-iodinase defect".
    Niepomniszcze H; Coleoni AH; Targovnik HM; Iorcansky S; Degrossi OJ
    Acta Endocrinol (Copenh); 1980 Jan; 93(1):25-31. PubMed ID: 7355662
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Thyroidal triiodothyronine and thyroxine in Graves' disease: correlation with presurgical treatment, thyroid status, and iodine content.
    Larsen PR
    J Clin Endocrinol Metab; 1975 Dec; 41(06):1098-104. PubMed ID: 54364
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Multiple effects of resorcinol on thyroid function (author's transl)].
    Berthezéne F; Perrot L; Munari Y; Ponsin G
    Ann Endocrinol (Paris); 1979; 40(1):67-8. PubMed ID: 443741
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Physiological significance of iodotyrosine-deiodinases].
    Voss C; Hartmann N
    Z Gesamte Inn Med; 1972 Mar; 27(5):193-7. PubMed ID: 4558910
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.