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"lin wd"的相关文件
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| 中山醫學大學 |
2021 |
Effects of Acrylamide-Induced Vasorelaxation and Neuromuscular Blockage: A Rodent Study
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Lin, WD; Ou, CC; Hsiao, SH; Chang, CH; Tsai, FJ; Liao, JW; Chen, YT |
| 中山醫學大學 |
2021 |
Is Preterm Birth a Risk Factor for Subsequent Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder in Children with Febrile Seizure?-A Retrospective Study
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Lin, CH; Lin, WD; Chou, IC; Lee, IC; Hong, SY |
| 中山醫學大學 |
2021 |
Association Between Kawasaki Disease and Childhood Epilepsy: A Nationwide Cohort Study in Taiwan
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Lin, CH; Lai, JN; Lee, IC; Chou, IC; Lin, WD; Lin, MC; Hong, SY |
| 國立交通大學 |
2014-12-08T15:45:13Z |
Comments on "Reliability and component importance of a consecutive-k-out-of-n system" by Zuo
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Hwang, FK; Cui, LR; Chang, JC; Lin, WD |
| 國立交通大學 |
2014-12-08T15:40:31Z |
A general construction for nonblocking crosstalk-free photonic switching networks
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Hwang, FK; Lin, WD |
| 國立交通大學 |
2014-12-08T15:40:01Z |
The incremental group testing model for gap closing in sequencing long molecules
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Hwang, FK; Lin, WD |
| 國立交通大學 |
2014-12-08T15:26:51Z |
A general construction for nonblocking crosstalk-free photonic switching networks
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Hwang, FK; Lin, WD |
| 國立交通大學 |
2014-12-08T15:17:55Z |
Necessary and sufficient conditions for rearrangeable Log(d) (N, m, p)
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Hwang, FK; Lin, WD |
| 中國醫藥大學 |
2005 |
Asymmetrical synthesis of L-homophenylalanine using engineered Escherichia coli aspartate aminotransferase
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Lo, HH; Hsu, SK; Lin, WD; Chan, NL; Hsu, WH |
| 中國醫藥大學 |
2004 |
Genetic and biochemical study in a patient with glutaric acidemia type I
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Lin, WD; Wang, CH; Lai, CC; Lee, CC; Tsai, FJ |
| 國立臺灣大學 |
2003-10 |
The development of a risk-adjusted capitation model based on principal inpatient diagnoses in Taiwan.
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Lin, WD; Chang, RE; Hsieh, CJ; Yaung, CL; Chiang, TL |
| 高雄醫學大學 |
2003 |
Anti-4-1BB-based immunotherapy for autoimmune diabetes: lessons from a transgenic non-obese diabetic (NOD) model.
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鄭添祿; Sytwu HK;Lin WD;Roffler SR;Hung JT;Sung HS;Wang CH;Cheng TL;Tsou SC;Hsi SC;Shen KL |
| 國立臺灣大學 |
2002-10 |
Healthcare utilization pattern and risk adjustment under Taiwan’s National Health Insurance system.
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Chang, RE; Lin, WD; Hsieh, CJ; Chiang, TL |
| 中國醫藥大學 |
2002 |
Monitoring of congenital adrenal hyperplasia by microbore HPLC-electrospray ionization tandem mass spectrometry of dried blood spots
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Lai, CC; Tsai, CH; Tsai, FJ; Wu, JY; Lin, WD; Lee, CC |
| 中國醫藥大學 |
2002 |
Monitoring of congenital adrenal hyperplasia by microbore HPLC-electrospray ionization tandem mass spectrometry of dried blood spots
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Lai, CC; Tsai, CH; Tsai, FJ; Wu, JY; Lin, WD; Lee, CC |
| 中國醫藥大學 |
2002 |
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
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Lai, CC; Tsai, CH; Tsai, FJ; Wu, JY; Lin, WD; Lee, CC |
| 中國醫藥大學 |
2002 |
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
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Lai, CC; Tsai, CH; Tsai, FJ; Wu, JY; Lin, WD; Lee, CC |
| 中國醫藥大學 |
2002 |
Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers
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Lin, WD; Wu, JY; Tsai, FJ; Gau, MT; Lee, CC |
| 中國醫藥大學 |
2002 |
Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers
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Lin, WD; Wu, JY; Tsai, FJ; Gau, MT; Lee, CC |
| 中國醫藥大學 |
2001 |
Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots
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Lai, CC; Tsai, CH; Tsai, FJ; Lee, CC; Lin, WD |
| 中國醫藥大學 |
2001 |
Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots
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Lai, CC; Tsai, CH; Tsai, FJ; Lee, CC; Lin, WD |
| 中國醫藥大學 |
2001 |
Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation
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Lin, WD; Wu, JY; Hsu, HB; Tsai, FJ; Lee, CC; Tsai, CH |
| 中國醫藥大學 |
2001 |
Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation
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Lin, WD; Wu, JY; Hsu, HB; Tsai, FJ; Lee, CC; Tsai, CH |
| 中國醫藥大學 |
2000 |
A stop codon mutation in the CBFA 1 gene causes cleidocranial dysplasia
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Tsai, FJ; Wu, JY; Lin, WD; Tsai, CH |
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