Wu TJ - Search Results

1

Homocystinuria in Taiwan: an inordinately high prevalence in an Austronesian aboriginal tribe, Tao.

Lu YH, Huang YH, Cheng LM, Yu HC, Hsu JH, Wu TJ, Lo MY, Lin A, Lin CY, Wu JY, Niu DM. Lu YH, et al. Among authors: wu jy, wu tj. Mol Genet Metab. 2012 Apr;105(4):590-5. doi: 10.1016/j.ymgme.2012.01.021. Epub 2012 Feb 1. Mol Genet Metab. 2012. PMID: 22353391

2

Heterozygous carriers of classical homocystinuria tend to have higher fasting serum homocysteine concentrations than non-carriers in the presence of folate deficiency.

Lu YH, Cheng LM, Huang YH, Lo MY, Wu TJ, Lin HY, Hsu TR, Niu DM. Lu YH, et al. Among authors: wu tj. Clin Nutr. 2015 Dec;34(6):1155-8. doi: 10.1016/j.clnu.2014.11.013. Epub 2014 Dec 3. Clin Nutr. 2015. PMID: 25516282

3

Clinical observations, molecular genetic analysis, and treatment of sitosterolemia in infants and children.

Niu DM, Chong KW, Hsu JH, Wu TJ, Yu HC, Huang CH, Lo MY, Kwok CF, Kratz LE, Ho LT. Niu DM, et al. Among authors: wu tj. J Inherit Metab Dis. 2010 Aug;33(4):437-43. doi: 10.1007/s10545-010-9126-2. Epub 2010 Jun 3. J Inherit Metab Dis. 2010. PMID: 20521169

4

Novel human pathological mutations. Gene symbol: GAA. Disease: glycogen storage disease 2.

Lin HY, Wu TJ, Hsu JH, Yu HC, Lin SP, Chuang CK, Huang CH, Niu DM. Lin HY, et al. Among authors: wu tj. Hum Genet. 2010 Apr;127(4):465. Hum Genet. 2010. PMID: 21488245 No abstract available.

5

Novel human pathological mutations. Gene symbol: GAA. Disease: glycogen storage disease 2.

Niu DM, Lin HY, Wu TJ, Hsu JH, Yu HC, Lin SP, Chuang CK, Huang CH. Niu DM, et al. Among authors: wu tj. Hum Genet. 2010 Apr;127(4):466. Hum Genet. 2010. PMID: 21488246 No abstract available.

6

Novel human pathological mutations. Gene symbol: GAA. Disease: glycogen storage disease 2.

Niu DM, Lin HY, Wu TJ, Hsu JH, Yu HC, Lin SP, Chuang CK, Huang CH. Niu DM, et al. Among authors: wu tj. Hum Genet. 2010 Apr;127(4):465. Hum Genet. 2010. PMID: 21488291 No abstract available.

7

Novel human pathological mutations. Gene symbol: GAA. Disease: glycogen storage disease 2.

Niu DM, Lin HY, Wu TJ, Hsu JH, Yu HC, Lin SP, Chuang CK, Huang CH. Niu DM, et al. Among authors: wu tj. Hum Genet. 2010 Apr;127(4):465. Hum Genet. 2010. PMID: 21488292 No abstract available.

8

Novel human pathological mutations. Gene symbol: GAA. Disease: glycogen storage disease 2.

Lin HY, Wu TJ, Hsu JH, Yu HC, Chuang CK, Huang CH, Niu DM. Lin HY, et al. Among authors: wu tj. Hum Genet. 2010 Apr;127(4):464. Hum Genet. 2010. PMID: 21488293 No abstract available.

9

The use of high resolution melting analysis to detect Fabry mutations in heterozygous females via dry bloodspots.

Tai CL, Liu MY, Yu HC, Chiang CC, Chiang H, Suen JH, Kao SM, Huang YH, Wu TJ, Yang CF, Tsai FC, Lin CY, Chang JG, Chen HD, Niu DM. Tai CL, et al. Among authors: wu tj. Clin Chim Acta. 2012 Feb 18;413(3-4):422-7. doi: 10.1016/j.cca.2011.10.023. Epub 2011 Oct 29. Clin Chim Acta. 2012. PMID: 22063097

10

Recessive congenital methemoglobinemia caused by a rare mechanism: maternal uniparental heterodisomy with segmental isodisomy of a chromosome 22.

Huang YH, Tai CL, Lu YH, Wu TJ, Chen HD, Niu DM. Huang YH, et al. Among authors: wu tj. Blood Cells Mol Dis. 2012 Aug 15;49(2):114-7. doi: 10.1016/j.bcmd.2012.05.005. Epub 2012 May 30. Blood Cells Mol Dis. 2012. PMID: 22658170

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