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 *

152 related articles for article (PubMed ID: 18681856)

  • 21. 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]  

  • 22. Activating TSH-receptor mutation (Met453Thr) as a cause of adenomatous non-autoimmune hyperthyroidism in a 3-year-old boy.
    Kraemer S; Rothe K; Pfaeffle R; Fuehrer-Sakel D; Till H; Muensterer OJ
    J Pediatr Endocrinol Metab; 2009 Mar; 22(3):269-74. PubMed ID: 19492584
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [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]  

  • 24. Novel TSHR germline mutation (Met463Val) masquerading as Graves' disease in a large Welsh kindred with hyperthyroidism.
    Fuhrer D; Warner J; Sequeira M; Paschke R; Gregory J; Ludgate M
    Thyroid; 2000 Dec; 10(12):1035-41. PubMed ID: 11201847
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Severe congenital non-autoimmune hyperthyroidism associated to a mutation in the extracellular domain of thyrotropin receptor gene.
    Scaglia PA; Chiesa A; Bastida G; Pacin M; Domené HM; Gruñeiro-Papendieck L
    Arq Bras Endocrinol Metabol; 2012 Nov; 56(8):513-8. PubMed ID: 23295291
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidism.
    Alberti L; Proverbio MC; Costagliola S; Weber G; Beck-Peccoz P; Chiumello G; Persani L
    Eur J Endocrinol; 2001 Sep; 145(3):249-54. PubMed ID: 11517004
    [TBL] [Abstract][Full Text] [Related]  

  • 28. An activating mutation of the thyrotropin receptor gene in hereditary non-autoimmune hyperthyroidism.
    Lee YS; Poh L; Loke KY
    J Pediatr Endocrinol Metab; 2002 Feb; 15(2):211-5. PubMed ID: 11874187
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Constitutively active germline mutation of the thyrotropin receptor gene as a cause of congenital hyperthyroidism.
    Schwab KO; Gerlich M; Broecker M; Söhlemann P; Derwahl M; Lohse MJ
    J Pediatr; 1997 Dec; 131(6):899-904. PubMed ID: 9427897
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A novel TSHR gene mutation (Ile691Phe) in a Chinese family causing autosomal dominant non-autoimmune hyperthyroidism.
    Liu Z; Sun Y; Dong Q; He M; Cheng CHK; Fan F
    J Hum Genet; 2008; 53(5):475-478. PubMed ID: 18306976
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Sporadic congenital hyperthyroidism due to a germline mutation in the thyrotropin receptor gene (Leu 512 Gln) in a Japanese patient.
    Nishihara E; Fukata S; Hishinuma A; Kudo T; Ohye H; Ito M; Kubota S; Amino N; Kuma K; Miyauchi A
    Endocr J; 2006 Dec; 53(6):735-40. PubMed ID: 16960398
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Re: "An activating mutation of the thyrotropin receptor gene in hereditary non-autoimmune hyperthyroidism" by Yung-Seng Lee et al. J Pediatr Endocrinol Metab 2002; 15: 211-215.
    Führer D; Gregory J; Ludgate M
    J Pediatr Endocrinol Metab; 2002; 15(9):1569; author reply 1569-70. PubMed ID: 12503868
    [No Abstract]   [Full Text] [Related]  

  • 33. Brief report: congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene.
    Kopp P; van Sande J; Parma J; Duprez L; Gerber H; Joss E; Jameson JL; Dumont JE; Vassart G
    N Engl J Med; 1995 Jan; 332(3):150-4. PubMed ID: 7800007
    [No Abstract]   [Full Text] [Related]  

  • 34. Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes.
    Camilot M; Teofoli F; Gandini A; Franceschi R; Rapa A; Corrias A; Bona G; Radetti G; Tatò L
    Clin Endocrinol (Oxf); 2005 Aug; 63(2):146-51. PubMed ID: 16060907
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Autosomal dominant nonautoimmune hyperthyroidism. Clinical features-diagnosis-therapy.
    Führer D; Mix M; Willgerodt H; Holzapfel HP; Von Petrykowski W; Wonerow P; Paschke R
    Exp Clin Endocrinol Diabetes; 1998; 106 Suppl 4():S10-5. PubMed ID: 9867189
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A Japanese family with nonautoimmune hyperthyroidism caused by a novel heterozygous thyrotropin receptor gene mutation.
    Nakamura A; Morikawa S; Aoyagi H; Ishizu K; Tajima T
    Pediatr Res; 2014 Jun; 75(6):749-53. PubMed ID: 24608569
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genetic hyperthyroidism: hyperthyroidism due to activating TSHR mutations.
    Hébrant A; van Staveren WC; Maenhaut C; Dumont JE; Leclère J
    Eur J Endocrinol; 2011 Jan; 164(1):1-9. PubMed ID: 20926595
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Constitutively activating TSH-receptor mutations as a molecular cause of non-autoimmune hyperthyroidism in childhood.
    Biebermann H; Schöneberg T; Krude H; Gudermann T; Grüters A
    Langenbecks Arch Surg; 2000 Oct; 385(6):390-2. PubMed ID: 11127522
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Squamosal Suture Craniosynostosis Due to Hyperthyroidism Caused by an Activating Thyrotropin Receptor Mutation (T632I).
    Chawla R; Alden TD; Bizhanova A; Kadakia R; Brickman W; Kopp PA
    Thyroid; 2015 Oct; 25(10):1167-72. PubMed ID: 26114856
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.