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.
150 related articles for article (PubMed ID: 17696839)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
14. 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]
15. A newly discovered TSHR variant (L665F) associated with nonautoimmune hyperthyroidism in an Austrian family induces constitutive TSHR activation by steric repulsion between TM1 and TM7. Jaeschke H; Schaarschmidt J; Eszlinger M; Huth S; Puttinger R; Rittinger O; Meiler J; Paschke R J Clin Endocrinol Metab; 2014 Oct; 99(10):E2051-9. PubMed ID: 24947036 [TBL] [Abstract][Full Text] [Related]
16. Late manifestation of subclinical hyperthyroidism after goitrogenesis in an index patient with a N670S TSH receptor germline mutation masquerading as TSH receptor antibody negative Graves' disease. Schaarschmidt J; Paschke S; Özerden M; Jäschke H; Huth S; Eszlinger M; Meller J; Paschke R Horm Metab Res; 2012 Dec; 44(13):962-5. PubMed ID: 22763653 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Subclinical nonautoimmune hyperthyroidism in a family segregates with a thyrotropin receptor mutation with weakly increased constitutive activity. Nishihara E; Chen CR; Higashiyama T; Mizutori-Sasai Y; Ito M; Kubota S; Amino N; Miyauchi A; Rapoport B Thyroid; 2010 Nov; 20(11):1307-14. PubMed ID: 20929407 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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] [Next] [New Search]