1. Léger J, Olivieri A, Donaldson M, Torresani T, Krude H, van Vliet G, et al. European Society for Paediatric Endocrinology consensus guidelines on screening, diagnosis, and management of congenital hypothyroidism. J Clin Endocrinol Metab. 2014; 99:363–84.
Article
2. Shapira SK, Hinton CF, Held PK, Jones E, Harry Hannon W, Ojodu J. Single newborn screen or routine second screening for primary congenital hypothyroidism. Mol Genet Metab. 2015; 116:125–32.
Article
3. Ford GA, Denniston S, Sesser D, Skeels MR, LaFranchi SH. Transient versus permanent congenital hypothyroidism after the age of 3 years in infants detected on the first versus second newborn screening test in Oregon, USA. Horm Res Paediatr. 2016; 86:169–77.
Article
4. Jones DE, Hart K, Shapira SK, Murray M, Atkinson-Dunn R, Rohrwasser A. Identification of primary congenital hypothyroidism based on two newborn screens - Utah, 2010-2016. MMWR Morb Mortal Wkly Rep. 2018; 67:782–5.
Article
5. Kilberg MJ, Rasooly IR, LaFranchi SH, Bauer AJ, Hawkes CP. Newborn screening in the US may miss mild persistent hypothyroidism. J Pediatr. 2018; 192:204–8.
Article
6. Woo HC, Lizarda A, Tucker R, Mitchell ML, Vohr B, Oh W, et al. Congenital hypothyroidism with a delayed thyroidstimulating hormone elevation in very premature infants: incidence and growth and developmental outcomes. J Pediatr. 2011; 158:538–42.
Article
7. Zung A, Yehieli A, Blau A, Almashanu S. Characteristics of Delayed thyroid stimulating hormone elevation in neonatal intensive care unit newborns. J Pediatr. 2016; 178:135–40. e1.
Article
8. Vigone MC, Caiulo S, Di Frenna M, Ghirardello S, Corbetta C, Mosca F, et al. Evolution of thyroid function in preterm infants detected by screening for congenital hypothyroidism. J Pediatr. 2014; 164:1296–302.
Article
9. McGrath N, Hawkes CP, Mayne P, Murphy NP. Optimal timing of repeat newborn screening for congenital hypothyroidism in preterm infants to detect delayed thyroid-stimulating hormone elevation. J Pediatr. 2019; 205:77–82.
Article
10. Nebesio TD, McKenna MP, Nabhan ZM, Eugster EA. Newborn screening results in children with central hypothyroidism. J Pediatr. 2010; 156:990–3.
Article
11. Zwaveling-Soonawala N, van Trotsenburg AS, Verkerk PH. The severity of congenital hypothyroidism of central origin should not be underestimated. J Clin Endocrinol Metab. 2015; 100:E297–300.
Article
12. Connelly KJ, LaFranchi SH. Detection of neonates with mild congenital hypothyroidism (primary) or isolated hyperthyrotropinemia: an increasingly common management dilemma. Expert Rev Endocrinol Metab. 2014; 9:263–71.
Article
13. LaFranchi SH. Approach to the diagnosis and treatment of neonatal hypothyroidism. J Clin Endocrinol Metab. 2011; 96:2959–67.
Article
14. American Academy of Pediatrics, Rose SR; Section on Endocrinology and Committee on Genetics; American Thyroid Association, Brown RS; Public Health Committee; Lawson Wilkins Pediatric Endocrine Society, Foley T, et al. Update of newborn screening and therapy for congenital hypothyroidism. Pediatrics. 2006; 117:2290–303.
Article
15. Schushan-Eisen I, Lazar L, Amitai N, Meyerovitch J. Thyroid functions in healthy infants during the first year of life. J Pediatr. 2016; 170:120–5. e1.
Article
16. Wassner AJ, Brown RS. Subclinical hypothyroidism in infancy: to treat or not to treat, that is the question. J Pediatr. 2016; 170:17–9.
Article
17. Braslavsky D, Méndez MV, Prieto L, Keselman A, Enacan R, Gruñeiro-Papendieck L, et al. Pilot neonatal screening program for central congenital hypothyroidism: evidence of significant detection. Horm Res Paediatr. 2017; 88:274–80.
Article
18. Ahmet A, Lawson ML, Babyn P, Tricco AC. Hypothyroidism in neonates post-iodinated contrast media: a systematic review. Acta Paediatr. 2009; 98:1568–74.
Article
19. Barr ML, Chiu HK, Li N, Yeh MW, Rhee CM, Casillas J, et al. Thyroid dysfunction in children exposed to iodinated contrast media. J Clin Endocrinol Metab. 2016; 101:2366–70.
Article
20. Cuestas E, Gaido MI, Capra RH. Transient neonatal hyperthyrotropinemia is a risk factor for developing persistent hyperthyrotropinemia in childhood with repercussion on developmental status. Eur J Endocrinol. 2015; 172:483–90.
Article
21. Lim HH, Yang SW. Risk factor for pituitary dysfunction in children and adolescents with Rathke's cleft cysts. Korean J Pediatr. 2010; 53:759–65.
Article
22. Schoenmakers N, Alatzoglou KS, Chatterjee VK, Dattani MT. Recent advances in central congenital hypothyroidism. J Endocrinol. 2015; 227:R51–71.
Article
23. Van den Berghe G, de Zegher F, Lauwers P. Dopamine suppresses pituitary function in infants and children. Crit Care Med. 1994; 22:1747–53.
Article
24. Tonyushkina KN, Krug S, Ortiz-Toro T, Mascari T, Karlstrom RO. Low thyroid hormone levels disrupt thyrotrope development. Endocrinology. 2017; 158:2774–82.
Article
25. Huang SA, Tu HM, Harney JW, Venihaki M, Butte AJ, Kozakewich HP, et al. Severe hypothyroidism caused by type 3 iodothyronine deiodinase in infantile hemangiomas. N Engl J Med. 2000; 343:185–9.
Article
26. Luongo C, Trivisano L, Alfano F, Salvatore D. Type 3 deiodinase and consumptive hypothyroidism: a common mechanism for a rare disease. Front Endocrinol (Lausanne). 2013; 4:115.
Article