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Journal Abstract Search

235 related items for PubMed ID: 9702065

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  • 3. Mutations in the mouse TSH receptor equivalent to human constitutively activating TSH receptor mutations also cause constitutive activity.
    Neumann S, Krohn K, Chey S, Paschke R.
    Horm Metab Res; 2001 May; 33(5):263-9. PubMed ID: 11440271
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  • 5. Premature birth and low birth weight associated with nonautoimmune hyperthyroidism due to an activating thyrotropin receptor gene mutation.
    Vaidya B, Campbell V, Tripp JH, Spyer G, Hattersley AT, Ellard S.
    Clin Endocrinol (Oxf); 2004 Jun; 60(6):711-8. PubMed ID: 15163335
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  • 6. Late manifestation of subclinical hyperthyroidism after goitrogenesis in an index patient with a N670S TSH receptor germline mutation masquerading as TSH receptor antibody negative Graves' disease.
    Schaarschmidt J, Paschke S, Özerden M, Jäschke H, Huth S, Eszlinger M, Meller J, Paschke R.
    Horm Metab Res; 2012 Dec; 44(13):962-5. PubMed ID: 22763653
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  • 7. Identification and evaluation of constitutively active thyroid stimulating hormone receptor mutations.
    Lado-Abeal J, Quisenberry LR, Castro-Piedras I.
    Methods Enzymol; 2010 Dec; 484():375-95. PubMed ID: 21036242
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  • 9. Thyrotropin receptor-associated diseases: from adenomata to Graves disease.
    Davies TF, Ando T, Lin RY, Tomer Y, Latif R.
    J Clin Invest; 2005 Aug; 115(8):1972-83. PubMed ID: 16075037
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  • 10. 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 Aug; 104 Suppl 4():117-20. PubMed ID: 8981017
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  • 11. Constitutively activating TSH receptor mutations as the cause of toxic thyroid adenoma, multinodular toxic goiter and autosomal dominant non autoimmune hyperthyroidism.
    Paschke R.
    Exp Clin Endocrinol Diabetes; 1996 Aug; 104 Suppl 4():129-32. PubMed ID: 8981020
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  • 13. Pathology of the TSH receptor.
    Duprez L, Parma J, Van Sande J, Rodien P, Sabine C, Abramowicz M, Dumont JE, Vassart G.
    J Pediatr Endocrinol Metab; 1999 Apr; 12 Suppl 1():295-302. PubMed ID: 10698593
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  • 14. [Pathologic manifestations of hormonal receptor mutations].
    Milgrom E.
    Bull Acad Natl Med; 2000 Apr; 184(3):605-16; discussion 617-9. PubMed ID: 10989556
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  • 15. Constitutively activating mutations of the thyrotropin receptor and thyroid disease.
    Führer D, Holzapfel HP, Wonerow P, Paschke R.
    Eur J Med Res; 1996 Jul 25; 1(10):460-4. PubMed ID: 9438142
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  • 16. Subclinical hyperthyroidism due to a thyrotropin receptor (TSHR) gene mutation (S505R).
    Pohlenz J, Pfarr N, Krüger S, Hesse V.
    Acta Paediatr; 2006 Dec 25; 95(12):1685-7. PubMed ID: 17129985
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  • 19. The detection of somatic mutations of thyrotropin receptor gene in fine needle biopsy samples from thyroid nodules.
    Syrenicz A, Kurzawski G, Ciechanowicz A.
    Endocr Regul; 1999 Sep 25; 33(3):95-101. PubMed ID: 10571960
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