BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 7618914)

  • 1. Thyroid ultrasonography in congenital isolated thyroid stimulating hormone deficiency.
    Wakamoto H; Miyazaki M; Tatsumi K; Amino N
    Arch Dis Child; 1995 May; 72(5):439-40. PubMed ID: 7618914
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene.
    Bretones P; Duprez L; Parma J; David M; Vassart G; Rodien P
    Thyroid; 2001 Oct; 11(10):977-80. PubMed ID: 11716047
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sonographic imaging of the thyroid gland in congenital hypothyroidism.
    Ueda D; Mitamura R; Suzuki N; Yano K; Okuno A
    Pediatr Radiol; 1992; 22(2):102-5. PubMed ID: 1501934
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rapid detection of a point mutation in thyroid-stimulating hormone beta-subunit gene causing congenital isolated thyroid-stimulating hormone deficiency.
    Mori R; Sawai T; Kinoshita E; Baba T; Matsumoto T; Yoshimoto M; Tsuji Y; Satake Y; Sawada K
    Jinrui Idengaku Zasshi; 1991 Dec; 36(4):313-6. PubMed ID: 1811097
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Congenital hypothyroid dwarfism in a family of giant schnauzers.
    Greco DS; Feldman EC; Peterson ME; Turner JL; Hodges CM; Shipman LW
    J Vet Intern Med; 1991; 5(2):57-65. PubMed ID: 2061865
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Neonatal thyroid disorders.
    Grüters A; Biebermann H; Krude H
    Horm Res; 2003; 59 Suppl 1():24-9. PubMed ID: 12566717
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The comparison of thyroxine versus thyroxine plus oral iodine in the treatment of congenital hypothyroidism due to iodine deficiency.
    Kurtoğlu S; Köroğlu Ş; Baştuğ O; Daar G; Yıkılmaz A; Elmalı F
    Horm Res Paediatr; 2014; 81(6):409-15. PubMed ID: 24776962
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Ultrasonography of the thyroid gland and the pancreas in healthy children and in patients with endocrinological disease].
    Ueda D
    Hokkaido Igaku Zasshi; 1991 Jan; 66(1):67-78. PubMed ID: 2004737
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dyshormonogenesis seems to be more frequent in a group of Cameroonian children with congenital hypothyroidism.
    Um Sap SN; Koki P; Dongmo FN; De Djob L; Tedga A; Awa HM; Chelo D; Boula A
    J Pediatr Endocrinol Metab; 2015 Sep; 28(9-10):1173-7. PubMed ID: 26030782
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pituitary cretinism in two sisters.
    Kohno H; Watanabe N; Ootsuka M; Kajiwara M; Gohya N
    Arch Dis Child; 1980 Sep; 55(9):725-7. PubMed ID: 7436542
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Incidence of iodine deficiency in Turkish patients with congenital hypothyroidism.
    Evliyaoğlu O; Kutlu A; Kara C; Atavci SG
    Pediatr Int; 2008 Jun; 50(3):276-80. PubMed ID: 18533935
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 19(10):1037-9. PubMed ID: 3932951
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Loss of integrity of thyroid morphology and function in children born to mothers with inadequately treated Graves' disease.
    Kempers MJ; van Trotsenburg AS; van Rijn RR; Smets AM; Smit BJ; de Vijlder JJ; Vulsma T
    J Clin Endocrinol Metab; 2007 Aug; 92(8):2984-91. PubMed ID: 17504907
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Congenital hypothyroidism due to defects of thyroid development and mild increase of TSH at screening: data from the Italian National Registry of infants with congenital hypothyroidism.
    Olivieri A; Corbetta C; Weber G; Vigone MC; Fazzini C; Medda E;
    J Clin Endocrinol Metab; 2013 Apr; 98(4):1403-8. PubMed ID: 23443814
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Transient congenital hypothyroidism due to thyroid-stimulating hormone receptor blocking antibodies: a case series.
    Evans C; Gregory JW; Barton J; Bidder C; Gibbs J; Pryce R; Al-Muzaffar I; Ludgate M; Warner J; John R; Moat SJ
    Ann Clin Biochem; 2011 Jul; 48(Pt 4):386-90. PubMed ID: 21606073
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.