These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

194 related articles for article (PubMed ID: 9349581)

  • 1. Congenital nonautoimmune hyperthyroidism in a nonidentical twin caused by a sporadic germline mutation in the thyrotropin receptor gene.
    Kopp P; Jameson JL; Roe TF
    Thyroid; 1997 Oct; 7(5):765-70. PubMed ID: 9349581
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sporadic congenital hyperthyroidism due to a spontaneous germline mutation in the thyrotropin receptor gene.
    Holzapfel HP; Wonerow P; von Petrykowski W; Henschen M; Scherbaum WA; Paschke R
    J Clin Endocrinol Metab; 1997 Nov; 82(11):3879-84. PubMed ID: 9360555
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hyperthyroidism caused by a germline activating mutation of the thyrotropin receptor gene: difficulties in diagnosis and therapy.
    Bertalan R; Sallai A; Sólyom J; Lotz G; Szabó I; Kovács B; Szabó E; Patócs A; Rácz K
    Thyroid; 2010 Mar; 20(3):327-32. PubMed ID: 20146656
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sporadic nonautoimmune congenital hyperthyroidism due to a strong activating mutation of the thyrotropin receptor gene.
    Tonacchera M; Agretti P; Rosellini V; Ceccarini G; Perri A; Zampolli M; Longhi R; Larizza D; Pinchera A; Vitti P; Chiovato L
    Thyroid; 2000 Oct; 10(10):859-63. PubMed ID: 11081252
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Novel thyrotropin receptor germline mutation (Ile568Val) in a Saxonian family with hereditary nonautoimmune hyperthyroidism.
    Claus M; Maier J; Paschke R; Kujat C; Stumvoll M; Führer D
    Thyroid; 2005 Sep; 15(9):1089-94. PubMed ID: 16187920
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of a new thyrotropin receptor germline mutation (Leu629Phe) in a family with neonatal onset of autosomal dominant nonautoimmune hyperthyroidism.
    Führer D; Wonerow P; Willgerodt H; Paschke R
    J Clin Endocrinol Metab; 1997 Dec; 82(12):4234-8. PubMed ID: 9398746
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Severe congenital hyperthyroidism caused by a germ-line neo mutation in the extracellular portion of the thyrotropin receptor.
    Grüters A; Schöneberg T; Biebermann H; Krude H; Krohn HP; Dralle H; Gudermann T
    J Clin Endocrinol Metab; 1998 May; 83(5):1431-6. PubMed ID: 9589634
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [From gene to disease; thyroid stimulating hormone receptor, hyperthyroidism and hypothyroidism].
    Wiersinga WM
    Ned Tijdschr Geneeskd; 2001 May; 145(18):869-71. PubMed ID: 11379397
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sporadic nonautoimmune neonatal hyperthyroidism due to A623V germline mutation in the thyrotropin receptor gene.
    Aycan Z; Ağladıoğlu SY; Ceylaner S; Cetinkaya S; Baş VN; Kendirici HN
    J Clin Res Pediatr Endocrinol; 2010; 2(4):168-72. PubMed ID: 21274318
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A new silent germline mutation of the TSH receptor: coexpression in a hyperthyroid family member with a second activating somatic mutation.
    Gozu HI; Mueller S; Bircan R; Krohn K; Ekinci G; Yavuzer D; Sargin H; Sargin M; Ones T; Gezen C; Orbay E; Cirakoglu B; Paschke R
    Thyroid; 2008 May; 18(5):499-508. PubMed ID: 18466076
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital hyperthyroidism caused by a solitary toxic adenoma harboring a novel somatic mutation (serine281-->isoleucine) in the extracellular domain of the thyrotropin receptor.
    Kopp P; Muirhead S; Jourdain N; Gu WX; Jameson JL; Rodd C
    J Clin Invest; 1997 Sep; 100(6):1634-9. PubMed ID: 9294132
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel activating mutation in transmembrane helix 6 of the thyrotropin receptor as cause of hereditary nonautoimmune hyperthyroidism.
    Nwosu BU; Gourgiotis L; Gershengorn MC; Neumann S
    Thyroid; 2006 May; 16(5):505-12. PubMed ID: 16756474
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sporadic congenital nonautoimmune hyperthyroidism caused by P639S mutation in thyrotropin receptor gene.
    Agretti P; De Marco G; Biagioni M; Iannilli A; Marigliano M; Pinchera A; Vitti P; Cherubini V; Tonacchera M
    Eur J Pediatr; 2012 Jul; 171(7):1133-7. PubMed ID: 22371259
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Germline mutations of TSH receptor gene as cause of nonautoimmune subclinical hypothyroidism.
    Alberti L; Proverbio MC; Costagliola S; Romoli R; Boldrighini B; Vigone MC; Weber G; Chiumello G; Beck-Peccoz P; Persani L
    J Clin Endocrinol Metab; 2002 Jun; 87(6):2549-55. PubMed ID: 12050212
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Long-term carbimazole treatment of neonatal nonautoimmune hyperthyroidism due to a new activating TSH receptor gene mutation (Ala428Val).
    Börgel K; Pohlenz J; Koch HG; Bramswig JH
    Horm Res; 2005; 64(4):203-8. PubMed ID: 16260895
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The first activating TSH receptor mutation in transmembrane domain 1 identified in a family with nonautoimmune hyperthyroidism.
    Biebermann H; Schöneberg T; Hess C; Germak J; Gudermann T; Grüters A
    J Clin Endocrinol Metab; 2001 Sep; 86(9):4429-33. PubMed ID: 11549687
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prolonged inappropriate TSH suppression during hypothyroidism after thyroid ablation in a patient with nonautoimmune familial hyperthyroidism.
    Jaeschke H; Eszlinger M; Lueblinghoff J; Coslovsky R; Paschke R
    Horm Metab Res; 2011 Jun; 43(7):500-4. PubMed ID: 21590647
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Shared sporadic and somatic thyrotropin receptor mutations display more active in vitro activities than familial thyrotropin receptor mutations.
    Lueblinghoff J; Eszlinger M; Jaeschke H; Mueller S; Bircan R; Gozu H; Sancak S; Akalin S; Paschke R
    Thyroid; 2011 Mar; 21(3):221-9. PubMed ID: 21190443
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.