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133 related items for PubMed ID: 8263143

  • 1. Familial unresponsiveness to thyrotropin by autosomal recessive inheritance.
    Takamatsu J, Nishikawa M, Horimoto M, Ohsawa N.
    J Clin Endocrinol Metab; 1993 Dec; 77(6):1569-73. PubMed ID: 8263143
    [Abstract] [Full Text] [Related]

  • 2. Congenital hypothyroidism with impaired thyroid response to thyrotropin (TSH) and absent circulating thyroglobulin: evidence for a new inactivating mutation of the TSH receptor gene.
    Tonacchera M, Agretti P, Pinchera A, Rosellini V, Perri A, Collecchi P, Vitti P, Chiovato L.
    J Clin Endocrinol Metab; 2000 Mar; 85(3):1001-8. PubMed ID: 10720030
    [Abstract] [Full Text] [Related]

  • 3. Sequence analysis of the thyrotropin (TSH) receptor gene in congenital primary hypothyroidism associated with TSH unresponsiveness.
    Takeshita A, Nagayama Y, Yamashita S, Takamatsu J, Ohsawa N, Maesaka H, Tachibana K, Tokuhiro E, Ashizawa K, Yokoyama N.
    Thyroid; 1994 Mar; 4(3):255-9. PubMed ID: 7833660
    [Abstract] [Full Text] [Related]

  • 4. Congenital hypothyroidism and apparent athyreosis with compound heterozygosity or compensated hypothyroidism with probable hemizygosity for inactivating mutations of the TSH receptor.
    Park SM, Clifton-Bligh RJ, Betts P, Chatterjee VK.
    Clin Endocrinol (Oxf); 2004 Feb; 60(2):220-7. PubMed ID: 14725684
    [Abstract] [Full Text] [Related]

  • 5. The hypothalamic-pituitary-thyroid negative feedback control axis in children with treated congenital hypothyroidism.
    Fisher DA, Schoen EJ, La Franchi S, Mandel SH, Nelson JC, Carlton EI, Goshi JH.
    J Clin Endocrinol Metab; 2000 Aug; 85(8):2722-7. PubMed ID: 10946871
    [Abstract] [Full Text] [Related]

  • 6. Subclinical hypothyroidism in early childhood: a frequent outcome of transient neonatal hyperthyrotropinemia.
    Calaciura F, Motta RM, Miscio G, Fichera G, Leonardi D, Carta A, Trischitta V, Tassi V, Sava L, Vigneri R.
    J Clin Endocrinol Metab; 2002 Jul; 87(7):3209-14. PubMed ID: 12107226
    [Abstract] [Full Text] [Related]

  • 7. Analysis of the promoter of the thyrotropin receptor gene and the entire genomic sequence of thyroid transcription factor-1 in familial congenital hypothyroidism due to thyrotropin unresponsiveness.
    Hishinuma A, Takamatsu J, Kanno Y, Yoshida S, Ieiri T.
    Thyroid; 1998 Apr; 8(4):305-9. PubMed ID: 9588495
    [Abstract] [Full Text] [Related]

  • 8. Apparent congenital athyreosis contrasting with normal plasma thyroglobulin levels and associated with inactivating mutations in the thyrotropin receptor gene: are athyreosis and ectopic thyroid distinct entities?
    Gagné N, Parma J, Deal C, Vassart G, Van Vliet G.
    J Clin Endocrinol Metab; 1998 May; 83(5):1771-5. PubMed ID: 9589691
    [Abstract] [Full Text] [Related]

  • 9. Congenital central hypothyroidism due to a homozygous mutation in the thyrotropin beta-subunit gene follows an autosomal recessive inheritance.
    Doeker BM, Pfäffle RW, Pohlenz J, Andler W.
    J Clin Endocrinol Metab; 1998 May; 83(5):1762-5. PubMed ID: 9589689
    [Abstract] [Full Text] [Related]

  • 10. Evaluation of the nocturnal serum thyrotropin (TSH) surge, as assessed by TSH ultrasensitive assay, in patients receiving long term L-thyroxine suppression therapy and in patients with various thyroid disorders.
    Bartalena L, Martino E, Falcone M, Buratti L, Grasso L, Mammoli C, Pacchiarotti A, Aghini-Lombardi F, Balzano S, Pinchera A.
    J Clin Endocrinol Metab; 1987 Dec; 65(6):1265-71. PubMed ID: 3680483
    [Abstract] [Full Text] [Related]

  • 11. Bioactivity of thyrotropin (TSH) in patients with central hypothyroidism: comparison between in vivo 3,5,3'-triiodothyronine response to TSH and in vitro bioactivity of TSH.
    Horimoto M, Nishikawa M, Ishihara T, Yoshikawa N, Yoshimura M, Inada M.
    J Clin Endocrinol Metab; 1995 Apr; 80(4):1124-8. PubMed ID: 7714080
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  • 13. Seasonal variation of serum thyrotropin concentration and thyrotropin response to thyrotropin-releasing hormone in patients with primary hypothyroidism on constant replacement dosage of thyroxine.
    Konno N, Morikawa K.
    J Clin Endocrinol Metab; 1982 Jun; 54(6):1118-24. PubMed ID: 6804476
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  • 14. The relationship of serum thyrotropin (TSH) to the thyroid hormones after oral TSH-releasing hormone in patients with preclinical hypothyroidism.
    Staub JJ, Noelpp B, Gräni R, Gemsenjäger E, Hauenstein M, Girard J.
    J Clin Endocrinol Metab; 1983 Mar; 56(3):449-53. PubMed ID: 6401757
    [Abstract] [Full Text] [Related]

  • 15. Structural analysis of the thyrotropin receptor in four patients with congenital hypothyroidism due to thyroid hypoplasia.
    Nogueira CR, Nguyen LQ, Coelho-Neto JR, Arseven OK, Jameson JL, Kopp P, Medeiros-Neto GA.
    Thyroid; 1999 Jun; 9(6):523-9. PubMed ID: 10411113
    [Abstract] [Full Text] [Related]

  • 16. Novel heterozygous thyrotropin receptor mutation presenting with neonatal hyperthyrotropinaemia, mild thyroid hypoplasia and absent uptake on radioisotope scan.
    Lucas-Herald A, Bradley T, Hermanns P, Jones J, Attaie M, Thompson E, Pohlenz J, Donaldson M.
    J Pediatr Endocrinol Metab; 2013 Jun; 26(5-6):583-6. PubMed ID: 23412867
    [Abstract] [Full Text] [Related]

  • 17. Free thyroid hormones in evaluating persistently elevated thyrotropin levels in children with congenital hypothyroidism on replacement therapy.
    Focarile F, Rondanini GF, Bollati A, Bartolucci A, Chiumello G.
    J Clin Endocrinol Metab; 1984 Dec; 59(6):1211-4. PubMed ID: 6490797
    [Abstract] [Full Text] [Related]

  • 18. Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland.
    Abramowicz MJ, Duprez L, Parma J, Vassart G, Heinrichs C.
    J Clin Invest; 1997 Jun 15; 99(12):3018-24. PubMed ID: 9185526
    [Abstract] [Full Text] [Related]

  • 19. Thyroid-stimulating hormone, prolactin, and growth hormone response to thyrotropin-releasing hormone in treated children with congenital hypothyroidism.
    Sack J, Shafrir Y, Urbach D, Amado O.
    Pediatr Res; 1985 Oct 15; 19(10):1037-9. PubMed ID: 3932951
    [Abstract] [Full Text] [Related]

  • 20. Pituitary-thyroid feedback in a patient with a sporadic activating thyrotropin (TSH) receptor mutation: implication that thyroid-secreted factors other than thyroid hormones contribute to serum TSH levels.
    Gelwane G, de Roux N, Chevenne D, Carel JC, Léger J.
    J Clin Endocrinol Metab; 2009 Aug 15; 94(8):2787-91. PubMed ID: 19454581
    [Abstract] [Full Text] [Related]

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