415 related articles for article (PubMed ID: 26416826)
1. Recent advances in central congenital hypothyroidism.
Schoenmakers N; Alatzoglou KS; Chatterjee VK; Dattani MT
J Endocrinol; 2015 Dec; 227(3):R51-71. PubMed ID: 26416826
[TBL] [Abstract][Full Text] [Related]
2. Central hypothyroidism in children.
García M; Fernández A; Moreno JC
Endocr Dev; 2014; 26():79-107. PubMed ID: 25231446
[TBL] [Abstract][Full Text] [Related]
3. DIAGNOSIS OF ENDOCRINE DISEASE: Congenital hypothyroidism: update and perspectives.
Peters C; van Trotsenburg ASP; Schoenmakers N
Eur J Endocrinol; 2018 Dec; 179(6):R297-R317. PubMed ID: 30324792
[TBL] [Abstract][Full Text] [Related]
4. Hypopituitarism oddities: congenital causes.
Kelberman D; Dattani MT
Horm Res; 2007; 68 Suppl 5():138-44. PubMed ID: 18174732
[TBL] [Abstract][Full Text] [Related]
5. Recent advances in research on isolated congenital central hypothyroidism.
Tajima T; Nakamura A; Oguma M; Yamazaki M
Clin Pediatr Endocrinol; 2019; 28(3):69-79. PubMed ID: 31384098
[TBL] [Abstract][Full Text] [Related]
6. Mechanisms related to the pathophysiology and management of central hypothyroidism.
Yamada M; Mori M
Nat Clin Pract Endocrinol Metab; 2008 Dec; 4(12):683-94. PubMed ID: 18941435
[TBL] [Abstract][Full Text] [Related]
7. Congenital Hypopituitarism During the Neonatal Period: Epidemiology, Pathogenesis, Therapeutic Options, and Outcome.
Bosch I Ara L; Katugampola H; Dattani MT
Front Pediatr; 2020; 8():600962. PubMed ID: 33634051
[No Abstract] [Full Text] [Related]
8. [From gene to disease; POU1F1- and PROP1-mutations in pituitary hormone deficiency].
Wit JM; Vulsma T; de Vijlder JJ
Ned Tijdschr Geneeskd; 2001 Dec; 145(50):2425-7. PubMed ID: 11776668
[TBL] [Abstract][Full Text] [Related]
9. A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism.
Koulouri O; Nicholas AK; Schoenmakers E; Mokrosinski J; Lane F; Cole T; Kirk J; Farooqi IS; Chatterjee VK; Gurnell M; Schoenmakers N
J Clin Endocrinol Metab; 2016 Mar; 101(3):847-51. PubMed ID: 26735259
[TBL] [Abstract][Full Text] [Related]
10. [Genetic aspects of growth hormone deficiency].
Reynaud R; Castinetti F; Galon-Faure N; Albarel-Loy F; Saveanu A; Quentien MH; Jullien N; Khammar A; Enjalbert A; Barlier A; Brue T
Arch Pediatr; 2011 Jun; 18(6):696-706. PubMed ID: 21497494
[TBL] [Abstract][Full Text] [Related]
11. Role of the thyrotropin-releasing hormone stimulation test in diagnosis of congenital central hypothyroidism in infants.
van Tijn DA; de Vijlder JJ; Vulsma T
J Clin Endocrinol Metab; 2008 Feb; 93(2):410-9. PubMed ID: 18000095
[TBL] [Abstract][Full Text] [Related]
12. Genetic forms of hypopituitarism and their manifestation in the neonatal period.
Alatzoglou KS; Dattani MT
Early Hum Dev; 2009 Nov; 85(11):705-12. PubMed ID: 19762173
[TBL] [Abstract][Full Text] [Related]
13. Pilot Neonatal Screening Program for Central Congenital Hypothyroidism: Evidence of Significant Detection.
Braslavsky D; Méndez MV; Prieto L; Keselman A; Enacan R; Gruñeiro-Papendieck L; Jullien N; Savenau A; Reynaud R; Brue T; Bergadá I; Chiesa A
Horm Res Paediatr; 2017; 88(3-4):274-280. PubMed ID: 28898885
[TBL] [Abstract][Full Text] [Related]
14. Central Hypothyroidism Due to a TRHR Mutation Causing Impaired Ligand Affinity and Transactivation of Gq.
García M; González de Buitrago J; Jiménez-Rosés M; Pardo L; Hinkle PM; Moreno JC
J Clin Endocrinol Metab; 2017 Jul; 102(7):2433-2442. PubMed ID: 28419241
[TBL] [Abstract][Full Text] [Related]
15. Neonatal screening for primary and central congenital hypothyroidism: is it time to go Dutch?
Boelen A; Zwaveling-Soonawala N; Heijboer AC; van Trotsenburg ASP
Eur Thyroid J; 2023 Jul; 12(4):. PubMed ID: 37326450
[TBL] [Abstract][Full Text] [Related]
16. Diagnosis and Management of Central Congenital Hypothyroidism.
Lauffer P; Zwaveling-Soonawala N; Naafs JC; Boelen A; van Trotsenburg ASP
Front Endocrinol (Lausanne); 2021; 12():686317. PubMed ID: 34566885
[TBL] [Abstract][Full Text] [Related]
17. Congenital isolated central hypothyroidism: Novel mutations and their functional implications.
Boelen A; van Trotsenburg ASP; Fliers E
Handb Clin Neurol; 2021; 180():161-169. PubMed ID: 34225927
[TBL] [Abstract][Full Text] [Related]
18. Gradual loss of ACTH due to a novel mutation in LHX4: comprehensive mutation screening in Japanese patients with congenital hypopituitarism.
Takagi M; Ishii T; Inokuchi M; Amano N; Narumi S; Asakura Y; Muroya K; Hasegawa Y; Adachi M; Hasegawa T
PLoS One; 2012; 7(9):e46008. PubMed ID: 23029363
[TBL] [Abstract][Full Text] [Related]
19. A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome.
Roche EF; McGowan A; Koulouri O; Turgeon MO; Nicholas AK; Heffernan E; El-Khairi R; Abid N; Lyons G; Halsall D; Bonomi M; Persani L; Dattani MT; Gurnell M; Bernard DJ; Schoenmakers N
Clin Endocrinol (Oxf); 2018 Dec; 89(6):813-823. PubMed ID: 30086211
[TBL] [Abstract][Full Text] [Related]
20. Newborn screening for congenital hypothyroidism.
Büyükgebiz A
J Pediatr Endocrinol Metab; 2006 Nov; 19(11):1291-8. PubMed ID: 17220056
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
