1. Lee DH. Neonatal screening for inborn errors of metabolism. J Korean Pediatr Soc. 1987; 30:9–16.
2. Lee DH. Newborn screening of inherited metabolic disease in Korea. Korean J pediatr. 2006; 49:1125–1139.
Article
3. Gurian EA, Kinnamon DD, Henry JJ, Waisbren SE. Expanded newborn screening for biochemical disorders: the effect of a false-positive result. Pediatrics. 2006; 117:1915–1921.
Article
4. Schulze A, Lindner M, Kohlmüller D, Olgemöller K, Mayatepek E, Hoffmann GF. Expanded newborn screening for inborn errors of metabolism by electrospray ionization-tandem mass spectrometry: results, outcome, and implications. Pediatrics. 2003; 111(6 Pt 1):1399–1406.
Article
5. Song JY, Son DW, Kim BI, Yang SW, Choi JH, Yoon CK, et al. Re-evaluation of TSH screening test in neonates. J Korean Pediatr Soc. 1993; 36:1502–1506.
6. Lee JM, Choi TY, Lee DW, Lee DH. Recheck rate, recall rate and reference range of the neonatal screening test for congenital hypothyroidism. J Clin Pathol Qual Control. 2001; 23:215–220.
7. Clinical and Laboratory Standards Institute. Newborn screening for preterm, low birth weight, and sick newborns; approved guideline. CLSI document NBS03-A. Wayne (PA): Clinical and Laboratory Standards Institute;2009.
8. Clinical and Laboratory Standards Institute. Newborn screening by tandem mass spectrometry; approved guideline. CLSI document NBS04-A. Wayne (PA): Clinical and Laboratory Standards Institute;2010.
9. Fant KE, Clark SJ, Kemper AR. Completeness and complexity of information available to parents from newborn-screening programs. Pediatrics. 2005; 115:1268–1272.
Article
10. Green JM, Hewison J, Bekker HL, Bryant LD, Cuckle HS. Psychosocial aspects of genetic screening of pregnant women and newborns: a systematic review. Health Technol Assess. 2004; 8:iiiix–x. 1–109.
Article
11. Kwon C, Farrell PM. The magnitude and challenge of false-positive newborn screening test results. Arch Pediatr Adolesc Med. 2000; 154:714–718.
Article
12. Bodegård G, Fyrö K, Larsson A. Psychological reactions in 102 families with a newborn who has a falsely positive screening test for congenital hypothyroidism. Acta Paediatr Scand Suppl. 1983; 304:1–21.
13. Essex MJ, Klein MH, Cho E, Kalin NH. Maternal stress beginning in infancy may sensitize children to later stress exposure: effects on cortisol and behavior. Biol Psychiatry. 2002; 52:776–784.
Article
14. Green M. Vulnerable child syndrome and its variants. Pediatr Rev. 1986; 8:75–80.
Article
15. Leslie LK, Boyce WT. Consultation with the specialist. The vulnerable child. Pediatr Rev. 1996; 17:323–326.
Article
16. Choi TY, Kim JW, Min WK, Lee DH. Analysis of blood sample records for neonatal screening test and external quality assessment for inborn errors of metabolism in Korea. J Korean Soc Matern Child Health. 2003; 7:7–17.
17. Lee DH. The prevalence of pediatric endocrine and metabolic diseases in Korea. Korean J Pediatr. 2008; 51:559–563.
Article
18. American College of Medical Genetics/American Society of Human Genetics Test and Technology Transfer Committee Working Group. Tandem mass spectrometry in newborn screening. American College of Medical Genetics/American Society of Human Genetics Test and Technology Transfer Committee Working Group. Genet Med. 2000; 2:267–269.
19. Matern D, Tortorelli S, Oglesbee D, Gavrilov D, Rinaldo P. Reduction of the false-positive rate in newborn screening by implementation of MS/MS-based second-tier tests: the Mayo Clinic experience (2004-2007). J Inherit Metab Dis. 2007; 30:585–592.
Article
20. Shim KS, Hwang JS, Lim JS, Kim SY, Shin CH, Yang SW, et al. Re-evaluation of neonatal screening tests for inborn errors of metabolism with dried filter paper blood spots. J Korean Pediatr Soc. 1999; 42:1639–1644.
21. Ensenauer R, Vockley J, Willard JM, Huey JC, Sass JO, Edland SD, et al. A common mutation is associated with a mild, potentially asymptomatic phenotype in patients with isovaleric acidemia diagnosed by newborn screening. Am J Hum Genet. 2004; 75:1136–1142.
Article
22. Matern D, He M, Berry SA, Rinaldo P, Whitley CB, Madsen PP, et al. Prospective diagnosis of 2-methylbutyryl-CoA dehydrogenase deficiency in the Hmong population by newborn screening using tandem mass spectrometry. Pediatrics. 2003; 112(1 Pt 1):74–78.
Article
23. Abdenur JE, Chamoles NA, Guinle AE, Schenone AB, Fuertes AN. Diagnosis of isovaleric acidaemia by tandem mass spectrometry: false positive result due to pivaloylcarnitine in a newborn screening programme. J Inherit Metab Dis. 1998; 21:624–630.
Article