220 related articles for article (PubMed ID: 17129985)
1. 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]
2. 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]
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. Mild congenital primary hypothyroidism in a Turkish family caused by a homozygous missense thyrotropin receptor (TSHR) gene mutation (A593 V).
Fricke-Otto S; Pfarr N; Mühlenberg R; Pohlenz J
Exp Clin Endocrinol Diabetes; 2005 Dec; 113(10):582-5. PubMed ID: 16320156
[TBL] [Abstract][Full Text] [Related]
5. Multiple relapses of hyperthyroidism after thyroid surgeries in a patient with long term follow-up of sporadic non-autoimmune hyperthyroidism.
Bircan R; Miehle K; Mladenova G; Ivanova R; Ivanova R; Sarafova A; Borissova AM; Lüblinghoff J; Paschke R
Exp Clin Endocrinol Diabetes; 2008 Jun; 116(6):341-6. PubMed ID: 18528812
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. [Non-autoimmune hyperthyroidism and hyperfunctioning thyroid adenomas caused by activating mutation of the thyrotropin receptor].
Kosugi S
Nihon Rinsho; 2002 Feb; 60(2):291-6. PubMed ID: 11857916
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. 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]
16. 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]
17. [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]
18. [Disorders caused by mutations of the thyrotropin receptor].
Kosugi S
Nihon Rinsho; 1998 Jul; 56(7):1856-60. PubMed ID: 9702065
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]