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.
184 related articles for article (PubMed ID: 12240901)
1. Similarities and differences in the phenotype of members of an Italian family with hereditary non-autoimmune hyperthyroidism associated with an activating TSH receptor germline mutation. Arturi F; Chiefari E; Tumino S; Russo D; Squatrito S; Chazenbalk G; Persani L; Rapoport B; Filetti S J Endocrinol Invest; 2002 Sep; 25(8):696-701. PubMed ID: 12240901 [TBL] [Abstract][Full Text] [Related]
2. A new case of familial nonautoimmune hyperthyroidism caused by the M463V mutation in the TSH receptor with anticipation of the disease across generations: a possible role of iodine supplementation. Ferrara AM; Capalbo D; Rossi G; Capuano S; Del Prete G; Esposito V; Montesano G; Zampella E; Fenzi G; Salerno M; Macchia PE Thyroid; 2007 Jul; 17(7):677-80. PubMed ID: 17696839 [TBL] [Abstract][Full Text] [Related]
3. Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene. Supornsilchai V; Sahakitrungruang T; Wongjitrat N; Wacharasindhu S; Suphapeetiporn K; Shotelersuk V Clin Endocrinol (Oxf); 2009 Apr; 70(4):623-8. PubMed ID: 18681856 [TBL] [Abstract][Full Text] [Related]
4. A family with a novel TSH receptor activating germline mutation (p.Ala485Val). Akcurin S; Turkkahraman D; Tysoe C; Ellard S; De Leener A; Vassart G; Costagliola S Eur J Pediatr; 2008 Nov; 167(11):1231-7. PubMed ID: 18175146 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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; 104 Suppl 4():129-32. PubMed ID: 8981020 [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. 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]
9. Prevalence of thyrotropin receptor germline mutations and clinical courses in 89 hyperthyroid patients with diffuse goiter and negative anti-thyrotropin receptor antibodies. Nishihara E; Fukata S; Hishinuma A; Amino N; Miyauchi A Thyroid; 2014 May; 24(5):789-95. PubMed ID: 24279482 [TBL] [Abstract][Full Text] [Related]
11. Genetics and phenomics of inherited and sporadic non-autoimmune hyperthyroidism. Gozu HI; Lublinghoff J; Bircan R; Paschke R Mol Cell Endocrinol; 2010 Jun; 322(1-2):125-34. PubMed ID: 20138963 [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. [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]
14. TSH receptor mutation V509A causes familial hyperthyroidism by release of interhelical constraints between transmembrane helices TMH3 and TMH5. Karges B; Krause G; Homoki J; Debatin KM; de Roux N; Karges W J Endocrinol; 2005 Aug; 186(2):377-85. PubMed ID: 16079263 [TBL] [Abstract][Full Text] [Related]
15. Novel germline mutation (Leu512Met) in the thyrotropin receptor gene (TSHR) leading to sporadic non-autoimmune hyperthyroidism. Roberts SA; Moon JE; Dauber A; Smith JR J Pediatr Endocrinol Metab; 2017 Mar; 30(3):343-347. PubMed ID: 28195550 [TBL] [Abstract][Full Text] [Related]
16. Mutations of the TSH receptor as cause of congenital hyperthyroidism. Schwab KO; Söhlemann P; Gerlich M; Broecker M; Petrykowski W; Holzapfel HP; Paschke R; Grüters A; Derwahl M Exp Clin Endocrinol Diabetes; 1996; 104 Suppl 4():124-8. PubMed ID: 8981019 [TBL] [Abstract][Full Text] [Related]
17. 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]
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. Genomic DNA analysis of thyrotropin receptor in a family with hereditary hyperthyroidism. Aoshima H; Yoshida T; Kobayashi S; Mizushima Y; Kawai S Endocr J; 2000 Jun; 47(3):365-72. PubMed ID: 11036883 [TBL] [Abstract][Full Text] [Related]