Lee CC - Search Results

1

Two novel mutations of the glycine receptor gene in a Taiwanese hyperekplexia family.

Tsai CH, Chang FC, Su YC, Tsai FJ, Lu MK, Lee CC, Kuo CC, Yang YW, Lu CS. Tsai CH, et al. Among authors: lee cc. Neurology. 2004 Sep 14;63(5):893-6. doi: 10.1212/01.wnl.0000138566.65519.67. Neurology. 2004. PMID: 15365143

2

Polymorphisms of the parkin gene in sporadic Parkinson's disease among Chinese in Taiwan.

Hu CJ, Sung SM, Liu HC, Lee CC, Tsai CH, Chang JG. Hu CJ, et al. Among authors: lee cc. Eur Neurol. 2000;44(2):90-3. doi: 10.1159/000008203. Eur Neurol. 2000. PMID: 10965160

3

Mutation analysis of type II Gaucher disease in five Taiwanese children: identification of two novel mutations.

Tsai FJ, Lee CC, Wu MC, Lin SP, Lin CY, Tsai CH, Kodama H, Wu JY. Tsai FJ, et al. Among authors: lee cc. Acta Paediatr Taiwan. 2001 Jul-Aug;42(4):231-5. Acta Paediatr Taiwan. 2001. PMID: 11550412

4

X-linked recessive myotubular myopathy proven by muscle biopsy.

Tsai CH, Huang WS, Tsai FJ, Lee CC, Chen SS. Tsai CH, et al. Among authors: lee cc. J Formos Med Assoc. 1996 Feb;95(2):153-6. J Formos Med Assoc. 1996. PMID: 9064005

5

Prenatal diagnosis of Apert syndrome.

Chang CC, Tsai FJ, Tsai HD, Tsai CH, Hseih YY, Lee CC, Yang TC, Wu JY. Chang CC, et al. Among authors: lee cc. Prenat Diagn. 1998 Jun;18(6):621-5. Prenat Diagn. 1998. PMID: 9664610

6

Mutation analysis of Wilson disease in Taiwan and description of six new mutations.

Tsai CH, Tsai FJ, Wu JY, Chang JG, Lee CC, Lin SP, Yang CF, Jong YJ, Lo MC. Tsai CH, et al. Among authors: lee cc. Hum Mutat. 1998;12(6):370-6. doi: 10.1002/(SICI)1098-1004(1998)12:6<370::AID-HUMU2>3.0.CO;2-S. Hum Mutat. 1998. PMID: 9829905

7

No association of alpha-2 macroglobulin gene five-nucleotide deletion with AD in Taiwan Chinese.

Hu CJ, Sung SM, Liu HC, Lee KY, Hsu WC, Wong WK, Lee CC, Tsai CH, Chang JG. Hu CJ, et al. Among authors: lee ky, lee cc. Neurology. 1999 Aug 11;53(3):642-3. doi: 10.1212/wnl.53.3.642. Neurology. 1999. PMID: 10449138

8

Insertion/deletion mutations of type I oculocutaneous albinism in chinese patients from Taiwan.

Tsai CH, Tsai FJ, Wu JY, Lin SP, Chang JG, Yang CF, Lee CC. Tsai CH, et al. Among authors: lee cc. Hum Mutat. 1999 Dec;14(6):542. doi: 10.1002/(SICI)1098-1004(199912)14:6<542::AID-HUMU14>3.0.CO;2-3. Hum Mutat. 1999. PMID: 10571953

9

A novel mutation (Q239R) identified in a Taiwan Chinese patient with type VI mucopolysaccharidosis (Maroteaux-Lamy syndrome).

Wu JY, Yang CF, Lee CC, Chang JG, Tsai FJ. Wu JY, et al. Among authors: lee cc. Hum Mutat. 2000 Apr;15(4):389-90. doi: 10.1002/(SICI)1098-1004(200004)15:4<389::AID-HUMU31>3.0.CO;2-0. Hum Mutat. 2000. PMID: 10738004 No abstract available.

10

An R223P mutation in EXT2 gene causes hereditary multiple exostoses.

Shi YR, Wu JY, Tsai FJ, Lee CC, Tsai CH. Shi YR, et al. Among authors: lee cc. Hum Mutat. 2000 Apr;15(4):390-1. doi: 10.1002/(SICI)1098-1004(200004)15:4<390::AID-HUMU35>3.0.CO;2-E. Hum Mutat. 2000. PMID: 10738008 No abstract available.

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