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Journal Abstract Search

211 related items for PubMed ID: 10895037

  • 1. Molecular pathogenesis of neonatal hypothyroidism.
    Krude H, Biebermann H, Schnabel D, Ambrugger P, Grüters A.
    Horm Res; 2000; 53 Suppl 1():12-8. PubMed ID: 10895037
    [Abstract] [Full Text] [Related]

  • 2.
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  • 3. Iodide handling disorders (NIS, TPO, TG, IYD).
    Targovnik HM, Citterio CE, Rivolta CM.
    Best Pract Res Clin Endocrinol Metab; 2017 Mar; 31(2):195-212. PubMed ID: 28648508
    [Abstract] [Full Text] [Related]

  • 4. The genetic characteristics of congenital hypothyroidism in China by comprehensive screening of 21 candidate genes.
    Sun F, Zhang JX, Yang CY, Gao GQ, Zhu WB, Han B, Zhang LL, Wan YY, Ye XP, Ma YR, Zhang MM, Yang L, Zhang QY, Liu W, Guo CC, Chen G, Zhao SX, Song KY, Song HD.
    Eur J Endocrinol; 2018 Jun; 178(6):623-633. PubMed ID: 29650690
    [Abstract] [Full Text] [Related]

  • 5. [Advances in genetic research of congenital hypothyroidism in China].
    Chen XY, Qin XS.
    Zhongguo Dang Dai Er Ke Za Zhi; 2018 Mar; 20(3):243-250. PubMed ID: 29530127
    [Abstract] [Full Text] [Related]

  • 6. Genetic basis of congenital hypothyroidism: abnormalities in the TSHbeta gene, the PIT1 gene, and the NIS gene.
    Tatsumi K, Miyai K, Amino N.
    Clin Chem Lab Med; 1998 Aug; 36(8):659-62. PubMed ID: 9806481
    [Abstract] [Full Text] [Related]

  • 7. Alterations of neonatal thyroid function.
    Grüters A, Krude H, Biebermann H, Liesenkötter KP, Schöneberg T, Gudermann T.
    Acta Paediatr Suppl; 1999 Feb; 88(428):17-22. PubMed ID: 10102047
    [Abstract] [Full Text] [Related]

  • 8. A novel mutation (Q40P) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia: evidence for phenotypic variability in mother and child.
    Congdon T, Nguyen LQ, Nogueira CR, Habiby RL, Medeiros-Neto G, Kopp P.
    J Clin Endocrinol Metab; 2001 Aug; 86(8):3962-7. PubMed ID: 11502839
    [Abstract] [Full Text] [Related]

  • 9. [The thyroid as a model for molecular mechanisms in genetic diseases].
    Rivolta CM, Moya CM, Esperante SA, Gutnisky VJ, Varela V, Targovnik HM.
    Medicina (B Aires); 2005 Aug; 65(3):257-67. PubMed ID: 16042141
    [Abstract] [Full Text] [Related]

  • 10. Genetic Evaluation of Congenital Hypothyroidism with Gland in situ Using Targeted Exome Sequencing.
    Shin JH, Kim HY, Kim YM, Lee H, Bae MH, Park KH, Lee SM, Kwak MJ.
    Ann Clin Lab Sci; 2021 Jan; 51(1):73-81. PubMed ID: 33653783
    [Abstract] [Full Text] [Related]

  • 11. [Molecular endocrinology of thyroid diseases].
    Meier CA.
    Schweiz Med Wochenschr; 1995 Dec 09; 125(49):2367-78. PubMed ID: 8848697
    [Abstract] [Full Text] [Related]

  • 12. Expression of thyroid-related genes in human thymus.
    Spitzweg C, Joba W, Heufelder AE.
    Thyroid; 1999 Feb 09; 9(2):133-41. PubMed ID: 10090312
    [Abstract] [Full Text] [Related]

  • 13. Screening for mutations of the human thyroid peroxidase gene in patients with congenital hypothyroidism.
    Grüters A, Köhler B, Wolf A, Söling A, de Vijlder L, Krude H, Biebermann H.
    Exp Clin Endocrinol Diabetes; 1996 Feb 09; 104 Suppl 4():121-3. PubMed ID: 8981018
    [Abstract] [Full Text] [Related]

  • 14. Congenital hypothyroidism: etiologies, diagnosis, and management.
    LaFranchi S.
    Thyroid; 1999 Jul 09; 9(7):735-40. PubMed ID: 10447022
    [Abstract] [Full Text] [Related]

  • 15.
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  • 16. Genetics of congenital hypothyroidism.
    Park SM, Chatterjee VK.
    J Med Genet; 2005 May 09; 42(5):379-89. PubMed ID: 15863666
    [Abstract] [Full Text] [Related]

  • 17. A novel mutation in the sodium/iodide symporter gene in the largest family with iodide transport defect.
    Kosugi S, Bhayana S, Dean HJ.
    J Clin Endocrinol Metab; 1999 Sep 09; 84(9):3248-53. PubMed ID: 10487695
    [Abstract] [Full Text] [Related]

  • 18. Genetic causes of congenital hypothyroidism due to dyshormonogenesis.
    Grasberger H, Refetoff S.
    Curr Opin Pediatr; 2011 Aug 09; 23(4):421-8. PubMed ID: 21543982
    [Abstract] [Full Text] [Related]

  • 19. Modulation of thyroid-specific gene expression in normal and nodular human thyroid tissues from adults: an in vivo effect of thyrotropin.
    Bruno R, Ferretti E, Tosi E, Arturi F, Giannasio P, Mattei T, Scipioni A, Presta I, Morisi R, Gulino A, Filetti S, Russo D.
    J Clin Endocrinol Metab; 2005 Oct 09; 90(10):5692-7. PubMed ID: 16076943
    [Abstract] [Full Text] [Related]

  • 20. Targeted next-generation sequencing of thirteen causative genes in Chinese patients with congenital hypothyroidism.
    Long W, Lu G, Zhou W, Yang Y, Zhang B, Zhou H, Jiang L, Yu B.
    Endocr J; 2018 Oct 29; 65(10):1019-1028. PubMed ID: 30022773
    [Abstract] [Full Text] [Related]

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