Lee NC - Search Results

1

Newborn screening for methylmalonic aciduria by tandem mass spectrometry: 7 years' experience from two centers in Taiwan.

Cheng KH, Liu MY, Kao CH, Chen YJ, Hsiao KJ, Liu TT, Lin HY, Huang CH, Chiang CC, Ho HJ, Lin SP, Lee NC, Hwu WL, Lin JL, Hung PY, Niu DM. Cheng KH, et al. Among authors: lee nc. J Chin Med Assoc. 2010 Jun;73(6):314-8. doi: 10.1016/S1726-4901(10)70067-8. J Chin Med Assoc. 2010. PMID: 20603089 Free article.

2

Neonatal bacteremia in a neonatal intensive care unit: analysis of causative organisms and antimicrobial susceptibility.

Lee NC, Chen SJ, Tang RB, Hwang BT. Lee NC, et al. J Chin Med Assoc. 2004 Jan;67(1):15-20. J Chin Med Assoc. 2004. PMID: 15077885

3

Contributions of bone maturation measurements to the differential diagnosis of neonatal transient hypothyroidism versus dyshormonogenetic congenital hypothyroidism.

Niu DM, Hwang B, Tiu CM, Tsai LP, Yen JL, Lee NC, Lin CY. Niu DM, et al. Among authors: lee nc. Acta Paediatr. 2004 Oct;93(10):1301-6. Acta Paediatr. 2004. PMID: 15499948

4

Alpha-galactosidase activity should be examined in patients with proteinuria: what have we learned from a family affected with Fabry disease?

Lee NC, Niu DM, Lin CY, Hsiao KJ, Yang AH, Ng YY. Lee NC, et al. Nephrol Dial Transplant. 2006 Feb;21(2):549-50. doi: 10.1093/ndt/gfi191. Epub 2005 Oct 12. Nephrol Dial Transplant. 2006. PMID: 16221700 No abstract available.

5

Long-term follow-up of Chinese patients who received delayed treatment for 6-pyruvoyl-tetrahydropterin synthase deficiency.

Lee NC, Cheng LY, Liu TT, Hsiao KJ, Chiu PC, Niu DM. Lee NC, et al. Mol Genet Metab. 2006 Feb;87(2):128-34. doi: 10.1016/j.ymgme.2005.09.028. Epub 2005 Dec 20. Mol Genet Metab. 2006. PMID: 16364672

6

Intrafamilial phenotype variation in Marfan syndrome ascertained by intragenic linkage analysis.

Lee NC, Hwang B, Chen CH, Niu DM. Lee NC, et al. J Formos Med Assoc. 2005 Dec;104(12):964-7. J Formos Med Assoc. 2005. PMID: 16607458

7

Time course of acylcarnitine elevation in neonatal intrahepatic cholestasis caused by citrin deficiency.

Lee NC, Chien YH, Kobayashi K, Saheki T, Chen HL, Chiu PC, Ni YH, Chang MH, Hwu WL. Lee NC, et al. J Inherit Metab Dis. 2006 Aug;29(4):551-5. doi: 10.1007/s10545-006-0250-y. Epub 2006 May 30. J Inherit Metab Dis. 2006. PMID: 16736097

8

Brain development in infantile-onset Pompe disease treated by enzyme replacement therapy.

Chien YH, Lee NC, Peng SF, Hwu WL. Chien YH, et al. Among authors: lee nc. Pediatr Res. 2006 Sep;60(3):349-52. doi: 10.1203/01.pdr.0000233014.84318.4e. Epub 2006 Jul 20. Pediatr Res. 2006. PMID: 16857770

9

Corneal lesion as the initial manifestation of tyrosinemia type II.

Tsai CP, Lin PY, Lee NC, Niu DM, Lee SM, Hsu WM. Tsai CP, et al. Among authors: lee nc, lee sm. J Chin Med Assoc. 2006 Jun;69(6):286-8. doi: 10.1016/S1726-4901(09)70259-X. J Chin Med Assoc. 2006. PMID: 16863017 Free article.

10

Acute metabolic decompensation and sudden death in Barth syndrome: report of a family and a literature review.

Yen TY, Hwu WL, Chien YH, Wu MH, Lin MT, Tsao LY, Hsieh WS, Lee NC. Yen TY, et al. Among authors: lee nc. Eur J Pediatr. 2008 Aug;167(8):941-4. doi: 10.1007/s00431-007-0592-y. Epub 2007 Sep 11. Eur J Pediatr. 2008. PMID: 17846786 Review.

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