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.
130 related articles for article (PubMed ID: 7800007)
1. 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]
2. 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]
3. 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]
4. Subclinical hyperthyroidism due to a thyrotropin receptor (TSHR) gene mutation (S505R). Pohlenz J; Pfarr N; Krüger S; Hesse V Acta Paediatr; 2006 Dec; 95(12):1685-7. PubMed ID: 17129985 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. Constitutively activating mutations of the thyrotropin receptor and thyroid disease. Führer D; Holzapfel HP; Wonerow P; Paschke R Eur J Med Res; 1996 Jul; 1(10):460-4. PubMed ID: 9438142 [TBL] [Abstract][Full Text] [Related]
11. Activating mutations of the thyrotropin receptor: a short review with emphasis on some pediatric aspects. Polak M Eur J Endocrinol; 1998 Apr; 138(4):353-7. PubMed ID: 9578496 [No Abstract] [Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Germline mutations in the thyrotropin receptor gene cause non-autoimmune autosomal dominant hyperthyroidism. Duprez L; Parma J; Van Sande J; Allgeier A; Leclère J; Schvartz C; Delisle MJ; Decoulx M; Orgiazzi J; Dumont J Nat Genet; 1994 Jul; 7(3):396-401. PubMed ID: 7920658 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]