262 related articles for article (PubMed ID: 28561265)
21. Sequence analysis of the thyrotropin (TSH) receptor gene in congenital primary hypothyroidism associated with TSH unresponsiveness.
Takeshita A; Nagayama Y; Yamashita S; Takamatsu J; Ohsawa N; Maesaka H; Tachibana K; Tokuhiro E; Ashizawa K; Yokoyama N
Thyroid; 1994; 4(3):255-9. PubMed ID: 7833660
[TBL] [Abstract][Full Text] [Related]
22. Genetics and phenomics of hypothyroidism due to TSH resistance.
Persani L; Calebiro D; Cordella D; Weber G; Gelmini G; Libri D; de Filippis T; Bonomi M
Mol Cell Endocrinol; 2010 Jun; 322(1-2):72-82. PubMed ID: 20083154
[TBL] [Abstract][Full Text] [Related]
23. Current loss-of-function mutations in the thyrotropin receptor gene: when to investigate, clinical effects, and treatment.
Cassio A; Nicoletti A; Rizzello A; Zazzetta E; Bal M; Baldazzi L
J Clin Res Pediatr Endocrinol; 2013; 5 Suppl 1(Suppl 1):29-39. PubMed ID: 23154162
[TBL] [Abstract][Full Text] [Related]
24. Eighteen-years follow-up of congenital hypothyroidism by
Watanabe D; Yagasaki H; Mitsui Y; Inukai T
Nagoya J Med Sci; 2023 May; 85(2):369-374. PubMed ID: 37346832
[TBL] [Abstract][Full Text] [Related]
25. The hypothalamic-pituitary-thyroid negative feedback control axis in children with treated congenital hypothyroidism.
Fisher DA; Schoen EJ; La Franchi S; Mandel SH; Nelson JC; Carlton EI; Goshi JH
J Clin Endocrinol Metab; 2000 Aug; 85(8):2722-7. PubMed ID: 10946871
[TBL] [Abstract][Full Text] [Related]
26. The R450H mutation and D727E polymorphism of the thyrotropin receptor gene in a Chinese child with congenital hypothyroidism.
Ma SG; Fang PH; Hong B; Yu WN
J Pediatr Endocrinol Metab; 2010 Dec; 23(12):1339-44. PubMed ID: 21714469
[TBL] [Abstract][Full Text] [Related]
27. Loss-of-function mutations in the thyrotropin receptor gene as a major determinant of hyperthyrotropinemia in a consanguineous community.
Tenenbaum-Rakover Y; Grasberger H; Mamanasiri S; Ringkananont U; Montanelli L; Barkoff MS; Dahood AM; Refetoff S
J Clin Endocrinol Metab; 2009 May; 94(5):1706-12. PubMed ID: 19240155
[TBL] [Abstract][Full Text] [Related]
28. Functional characterization of the novel sequence variant p.S304R in the hinge region of TSHR in a congenital hypothyroidism patients and analogy with other formerly known mutations of this gene portion.
Cerqueira TL; Carré A; Chevrier L; Szinnai G; Tron E; Léger J; Cabrol S; Queinnec C; De Roux N; Castanet M; Polak M; Ramos HE
J Pediatr Endocrinol Metab; 2015 Jul; 28(7-8):777-84. PubMed ID: 25153578
[TBL] [Abstract][Full Text] [Related]
29. The different requirement of L-T4 therapy in congenital athyreosis compared with adult-acquired hypothyroidism suggests a persisting thyroid hormone resistance at the hypothalamic-pituitary level.
Bagattini B; Cosmo CD; Montanelli L; Piaggi P; Ciampi M; Agretti P; Marco GD; Vitti P; Tonacchera M
Eur J Endocrinol; 2014 Nov; 171(5):615-21. PubMed ID: 25305309
[TBL] [Abstract][Full Text] [Related]
30. The syndrome of resistance to thyroid stimulating hormone.
Refetoff S
J Chin Med Assoc; 2003 Aug; 66(8):441-52. PubMed ID: 14604307
[TBL] [Abstract][Full Text] [Related]
31. Hypothyroidism in thyroid transcription factor 1 haploinsufficiency is caused by reduced expression of the thyroid-stimulating hormone receptor.
Moeller LC; Kimura S; Kusakabe T; Liao XH; Van Sande J; Refetoff S
Mol Endocrinol; 2003 Nov; 17(11):2295-302. PubMed ID: 12907760
[TBL] [Abstract][Full Text] [Related]
32. Biochemical, radiological, and genetic characterization of congenital hypothyroidism in Abu Dhabi, United Arab Emirates.
Deeb A; Elkadry I; Attia S; Al Suwaidi H; Obaid L; Schoenmakers NA
J Pediatr Endocrinol Metab; 2016 Jul; 29(7):801-6. PubMed ID: 27060741
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. The gene for the thyrotropin receptor (TSHR) as a candidate gene for congenital hypothyroidism with thyroid dysgenesis.
Krude H; Biebermann H; Göpel W; Grüters A
Exp Clin Endocrinol Diabetes; 1996; 104 Suppl 4():117-20. PubMed ID: 8981017
[TBL] [Abstract][Full Text] [Related]
35. Novel heterozygous thyrotropin receptor mutation presenting with neonatal hyperthyrotropinaemia, mild thyroid hypoplasia and absent uptake on radioisotope scan.
Lucas-Herald A; Bradley T; Hermanns P; Jones J; Attaie M; Thompson E; Pohlenz J; Donaldson M
J Pediatr Endocrinol Metab; 2013; 26(5-6):583-6. PubMed ID: 23412867
[TBL] [Abstract][Full Text] [Related]
36.
Zhang HY; Wu FY; Li XS; Tu PH; Zhang CX; Yang RM; Cui RJ; Wu CY; Fang Y; Yang L; Song HD; Zhao SX
Ann Lab Med; 2024 Jul; 44(4):343-353. PubMed ID: 38433572
[TBL] [Abstract][Full Text] [Related]
37. Resistance to thyrotropin (TSH) in three families is not associated with mutations in the TSH receptor or TSH.
Xie J; Pannain S; Pohlenz J; Weiss RE; Moltz K; Morlot M; Asteria C; Persani L; Beck-Peccoz P; Parma J; Vassart G; Refetoff S
J Clin Endocrinol Metab; 1997 Dec; 82(12):3933-40. PubMed ID: 9398691
[TBL] [Abstract][Full Text] [Related]
38. Effects of serum TSH and FT4 levels and the TSHR-Asp727Glu polymorphism on bone: the Rotterdam Study.
van der Deure WM; Uitterlinden AG; Hofman A; Rivadeneira F; Pols HA; Peeters RP; Visser TJ
Clin Endocrinol (Oxf); 2008 Feb; 68(2):175-81. PubMed ID: 17803697
[TBL] [Abstract][Full Text] [Related]
39. Natural history of mild subclinical hypothyroidism: prognostic value of ultrasound.
Rosário PW; Bessa B; Valadão MM; Purisch S
Thyroid; 2009 Jan; 19(1):9-12. PubMed ID: 19021461
[TBL] [Abstract][Full Text] [Related]
40. Molecular screening of the TSH receptor (TSHR) and thyroid peroxidase (TPO) genes in Korean patients with nonsyndromic congenital hypothyroidism.
Lee ST; Lee DH; Kim JY; Kwon MJ; Kim JW; Hong YH; Lee YW; Ki CS
Clin Endocrinol (Oxf); 2011 Nov; 75(5):715-21. PubMed ID: 21707688
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]