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Journal Abstract Search

327 related items for PubMed ID: 8981018

  • 1. 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; 104 Suppl 4():121-3. PubMed ID: 8981018
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  • 5. Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in Israelis.
    Tenenbaum-Rakover Y, Mamanasiri S, Ris-Stalpers C, German A, Sack J, Allon-Shalev S, Pohlenz J, Refetoff S.
    Clin Endocrinol (Oxf); 2007 May; 66(5):695-702. PubMed ID: 17381485
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  • 7. The gene for the thyrotropin receptor (TSHR) as a candidate gene for congenital hypothyroidism with thyroid dysgenesis.
    Krude H, Biebermann H, Göpel W, Grüters A.
    Exp Clin Endocrinol Diabetes; 1996 May; 104 Suppl 4():117-20. PubMed ID: 8981017
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  • 8. Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2 (THOX2) gene.
    Pfarr N, Korsch E, Kaspers S, Herbst A, Stach A, Zimmer C, Pohlenz J.
    Clin Endocrinol (Oxf); 2006 Dec; 65(6):810-5. PubMed ID: 17121535
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  • 9. Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidism.
    Moreno JC, Bikker H, Kempers MJ, van Trotsenburg AS, Baas F, de Vijlder JJ, Vulsma T, Ris-Stalpers C.
    N Engl J Med; 2002 Jul 11; 347(2):95-102. PubMed ID: 12110737
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  • 10. Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter.
    Abramowicz MJ, Targovnik HM, Varela V, Cochaux P, Krawiec L, Pisarev MA, Propato FV, Juvenal G, Chester HA, Vassart G.
    J Clin Invest; 1992 Oct 11; 90(4):1200-4. PubMed ID: 1401057
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  • 16. [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 Oct 11; 65(3):257-67. PubMed ID: 16042141
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  • 17. Congenital goitrous primary hypothyroidism in two German families caused by novel thyroid peroxidase (TPO) gene mutations.
    Altmann K, Hermanns P, Mühlenberg R, Fricke-Otto S, Wentzell R, Pohlenz J.
    Exp Clin Endocrinol Diabetes; 2013 Jun 11; 121(6):343-6. PubMed ID: 23512414
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  • 19. Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidism.
    Ambrugger P, Stoeva I, Biebermann H, Torresani T, Leitner C, Grüters A.
    Eur J Endocrinol; 2001 Jul 11; 145(1):19-24. PubMed ID: 11415848
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  • 20. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 11; 56(3):105-52. PubMed ID: 19728970
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