Lee CC - Search Results

1

Interleukin gene polymorphisms in age-related macular degeneration.

Tsai YY, Lin JM, Wan L, Lin HJ, Tsai Y, Lee CC, Tsai CH, Tsai FJ, Tseng SH. Tsai YY, et al. Among authors: lee cc. Invest Ophthalmol Vis Sci. 2008 Feb;49(2):693-8. doi: 10.1167/iovs.07-0125. Invest Ophthalmol Vis Sci. 2008. PMID: 18235016

2

Monitoring of congenital adrenal hyperplasia by microbore HPLC-electrospray ionization tandem mass spectrometry of dried blood spots.

Lai CC, Tsai CH, Tsai FJ, Wu JY, Lin WD, Lee CC. Lai CC, et al. Among authors: lee cc. Clin Chem. 2002 Feb;48(2):354-6. Clin Chem. 2002. PMID: 11805018 No abstract available.

3

Rapid screening assay of congenital adrenal hyperplasia by measuring 17 alpha-hydroxyprogesterone with high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots.

Lai CC, Tsai CH, Tsai FJ, Wu JY, Lin WD, Lee CC. Lai CC, et al. Among authors: lee cc. J Clin Lab Anal. 2002;16(1):20-5. doi: 10.1002/jcla.2039. J Clin Lab Anal. 2002. PMID: 11835526 Free PMC article.

4

Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method.

Shi YR, Hsieh KS, Wu JY, Lee CC, Tsai CH, Tsai FJ. Shi YR, et al. Among authors: lee cc. Pediatr Int. 2002 Jun;44(3):264-8. doi: 10.1046/j.1442-200x.2002.01553.x. Pediatr Int. 2002. PMID: 11982893

5

Interleukin-4 intron 3 polymorphism is not related to susceptibility to febrile seizures.

Tsai FJ, Chou IC, Hsieh YY, Lee CC, Lin CC, Tsai CH. Tsai FJ, et al. Among authors: lee cc. Pediatr Neurol. 2002 Oct;27(4):271-4. doi: 10.1016/s0887-8994(02)00434-4. Pediatr Neurol. 2002. PMID: 12435565

6

A novel nonsense mutation of the sedlin gene in a family with spondyloepiphyseal dysplasia tarda.

Shi YR, Lee CC, Hsu YA, Wang CH, Tsai FJ. Shi YR, et al. Among authors: lee cc. Hum Hered. 2002;54(1):54-6. doi: 10.1159/000066694. Hum Hered. 2002. PMID: 12446987

7

Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan.

Shi YR, Wu JY, Hsu YA, Lee CC, Tsai CH, Tsai FJ. Shi YR, et al. Among authors: lee cc. Genet Test. 2002 Fall;6(3):237-43. doi: 10.1089/109065702761403441. Genet Test. 2002. PMID: 12490068

8

Genetic analysis of chromosome 22q11.2 markers in congenital heart disease.

Shi YR, Hsieh KS, Wu JY, Lee CC, Tsai CH, Yu MT, Chang JS, Tsai FJ. Shi YR, et al. Among authors: lee cc. J Clin Lab Anal. 2003;17(1):28-35. doi: 10.1002/jcla.10062. J Clin Lab Anal. 2003. PMID: 12526020 Free PMC article.

9

Association of the neuronal nicotinic acetylcholine receptor subunit alpha4 polymorphisms with febrile convulsions.

Chou IC, Lee CC, Huang CC, Wu JY, Tsai JJ, Tsai CH, Tsai FJ. Chou IC, et al. Among authors: lee cc. Epilepsia. 2003 Aug;44(8):1089-93. doi: 10.1046/j.1528-1157.2003.t01-1-44702.x. Epilepsia. 2003. PMID: 12887442 Free article.

10

Brain-derived neurotrophic factor (BDNF) Val66Met polymorphisms in febrile seizures.

Chou IC, Tsai CH, Lee CC, Lin SS, Tsai FJ. Chou IC, et al. Among authors: lee cc. Epilepsy Res. 2004 Jun;60(1):27-9. doi: 10.1016/j.eplepsyres.2004.05.001. Epilepsy Res. 2004. PMID: 15279867

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