1 |
Lee DH. Neonatal screening in Korea, In: New trends in neonatal screening. Hokkaido Univ. press, 1994;3-5
|
2 |
Lee HJ, Moon HR, Shin YS. Clinical approach of inherited metabolic disease. Orombo 1990;152-7
|
3 |
Lee DH. Neonatal screening for inborn errors of metabolism. J of Kor Pediatr Association 1987;30:9-16
|
4 |
Cheon KS, Lee DH. Isovaleric Acidemia in Siblings Diagnosed by Organic Acid Analysis. J of the Kor Pediatr Society 2000;43:828-31
|
5 |
Kim SH, Suh ES, Lee DH. EEG in Phenylketonuria. J of the Kor Pediatr Society 40:759-766, 1997
|
6 |
Chong CH, Lee HY, Lee DH, Lee SJ, Cha KW, Yim JB,et al. Pterin and DHPR Measurement and DNA Analysis in Korean PKU Patients. J of Kor Pediatr Society 1993;36:1681-90
|
7 |
Park IS, Cho HJ, Lee DH and Song SH. Galactosemia Detected by Neonatal Screening Test. J Korean Pediatr Soc 2003;46:440-6
|
8 |
Hahn SH, Lee DH. Pilot study of mass screening for Wilson's disease in Korea. Molecular Genetics and Metabolism 2002;76:133-6
DOI
ScienceOn
|
9 |
Yoon HC, Kim NC, Lee DH. A cost-Benefit analysis on neonatal screening of phenylketonuria and congenital hypothyroidism in Korea. Korean J Pediatr 2005;48:369-75
|
10 |
Choi TY, Kim WB, Kang DY, Lee DH. A Case of Homocystinuria. Kor. J. of Clinical Pathology 13:351-6, 1993
|
11 |
Bickel H, Guthrie R, Hammersen G. Neonatal screening for inborn error of metabolism. Springer-Verlag, 1980;1-79
|
12 |
Moon DS, Kim DW, Lee DH, Lee SJ, You KS, Moon HR, et al. Cost-Benefit analysis of newborn mass screening for phenylketonuria and congenital hypothyroidism in Korea. J. of Soonchunhyang Medical College 1: 459-470, 1995
|
13 |
Lee DH. Clinical Experience in Dietary Management of Phenylketonuria with Maeil PKU-1, PKU-2 Formula. J Korean Soc of Inherited Metabolic Disease 2002;2:89-94
|
14 |
Hong HS, Kim DH, Lee HK, Kwon KH, Choi DL, Lee DH. MR Imaging of Phenylketonuria. J of the Kor Radiol Soc 1997;37:541-5
과학기술학회마을
DOI
|
15 |
Yoon HR, Lee KR, Kang SW, Lee DW, Yoo HW, Min WK, et al. Screening of newborns and high-risk group of children for inbom metabolic disorders using tandem mass spectrometry in South Korea: a three-year report. Clinica Chimica Acta 2005;354:167-80
DOI
ScienceOn
|
16 |
Choi TY, Kim JW, Min WK, Lee DH, et al. Analysis of Blood Sample Records for Neonatal Screening Test and External Quality Assessment for Inborn Errors of Metabolism in Korea. J Korean Soc of Maternal and CHild Health 2003;7:7-17
|
17 |
Lee DH. Recent Advances in Treatment of Inherited Metabolic Diseases. The J of the Kor Medical Association 1988;31:1267-73
|
18 |
Kenneth AP. US Newborn Screening System Guildlines II:Follow-ip of Children, Diagnosis, Management, and Evaluation, The Journal of Pediatrics 2000;137:S1-S46
DOI
|
19 |
Lee DH, Jang KA, Lee SJ, Yoo H. The Incidence of inborn error of metabolism and hypothyroidism in Korean newborns. The J of Soonchunhyang University 1988;11:201-9
|
20 |
Schoen EJ, Baker JC, Colby CJ, To TT. Cost-benefit analysis of universal tandem mass spectrometry for newborn screening. Pediatrics 2002;110:781-6
DOI
ScienceOn
|
21 |
Nam HG, Shim JS, Lee DH, and Lee SJ. A Clinical Study in Phenylketonuria. J of Kor Pediatr Association 1992;35:69-79
|
22 |
Ryoo HO, Lee DH. Cost-benefit analysis of universal tandem mass spectrometry for newborn screening in Korea. Program and abstracts 56th annual fall meeting of the Korean Pediatrics Society, 2005:77
|
23 |
Lee DH. Neonatal screening test. J of the Kor Medical Association 1994;37:1464-80
|
24 |
Hahn YJ, Lee DH, Kim ES. Plans to improve the mass screening tests on inborn errors of metabolism in Korea. Korean public health and society reserch center in 송 department of ministry of health and wellfare in Korea, 2000:51-68
|
25 |
Park KH, Lee YK, Choi TY, Kim WB, LeeDH. Seven cases of ornithine transcarbamylase deficiency. Kor J of Clinical Pathology 1999;19:308-14
|
26 |
Hong HK, Lee WR, Lee DH. A Case of Maternal Phenyketonuria. The Kor J of Perinatol 1999;10:387-90
|