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機構	日期	題名	作者
中國醫藥大學	2000	Longitudinal Doppler sonographic measurements of vascular impedance in the central and peripheral spiral arteries throughout pregnancy	Hsieh, YY; Chang, CC; Tsai, HD; Lee, CC; Tsai, CH
中國醫藥大學	2000	Longitudinal Doppler sonographic measurements of vascular impedance in the central and peripheral spiral arteries throughout pregnancy	Hsieh, YY; Chang, CC; Tsai, HD; Lee, CC; Tsai, CH
中國醫藥大學	2000	Lewis (FUT3) genotypes in Taiwanese, Thai, and Filipino populations	Liu, TC; Chang, JG; Lin, SF; Chang, WC; Yang, TY; Lin, CL; Wang, NM; Tsai, CH
中國醫藥大學	2000	Lewis (FUT3) genotypes in Taiwanese, Thai, and Filipino populations	Liu, TC; Chang, JG; Lin, SF; Chang, WC; Yang, TY; Lin, CL; Wang, NM; Tsai, CH
中國醫藥大學	2000	G protein beta 3 subunit variant and essential hypertension in Taiwan - a case-control study	Tsai, CH; Yeh, HI; Chou, YS; Liu, HF; Yang, TY; Wang, JC; Wang, NM; Chang, JG
中國醫藥大學	2000	Genetic risk factors of sporadic Alzheimer's disease among Chinese in Taiwan	Hu, CJ; Sung, SM; Liu, HC; Hsu, WC; Lee, LS; Lee, CC; Tsai, CH; Chang, JG
中國醫藥大學	2000	Genetic risk factors of sporadic Alzheimer's disease among Chinese in Taiwan	Hu, CJ; Sung, SM; Liu, HC; Hsu, WC; Lee, LS; Lee, CC; Tsai, CH; Chang, JG
中國醫藥大學	2000	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
中國醫藥大學	2000	Analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency	Lee, HH; Chang, JG; Tsai, CH; Tsai, FJ; Chao, HT; Chung, BC
中國醫藥大學	2000	No evidence of correlation between mutation at codon 531 of src and the risk of colon cancer in Chinese	Wang, NM; Yeh, KT; Tsai, CH; Chen, SJ; Chang, JG
中國醫藥大學	2000	Analysis of the mRNA transcripts of the survival motor neuron (SMN) gene in the tissue of an SMA fetus and the peripheral blood mononuclear cells of normals, carriers and SMA patients	Jong, YJ; Chang, JG; Lin, SP; Yang, TY; Wang, JC; Chang, CP; Lee, CC; Li, H; Hsieh-Li, HM; Tsai, CH
中國醫藥大學	2000	Analysis of the mRNA transcripts of the survival motor neuron (SMN) gene in the tissue of an SMA fetus and the peripheral blood mononuclear cells of normals, carriers and SMA patients	Jong, YJ; Chang, JG; Lin, SP; Yang, TY; Wang, JC; Chang, CP; Lee, CC; Li, H; Hsieh-Li, HM; Tsai, CH
中國醫藥大學	2000	Carrier analysis and prenatal diagnosis of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in Chinese	Lee, HH; Kuo, JM; Chao, HT; Lee, YJ; Chang, JG; Tsai, CH; Chung, BC
中國醫藥大學	2000	Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in cervical cancer	Su, TH; Chang, JG; Perng, LI; Chang, CP; Wei, HJ; Wang, NM; Tsai, CH
中國醫藥大學	2000	A mouse model for spinal muscular atrophy	Hsieh-Li, HM; Chang, JG; Jong, YJ; Wu, MH; Wang, NM; Tsai, CH; Li, H
中國醫藥大學	2000	A mouse model for spinal muscular atrophy	Hsieh-Li, HM; Chang, JG; Jong, YJ; Wu, MH; Wang, NM; Tsai, CH; Li, H
中國醫藥大學	2000	Epidemiologic features of rotavirus infection in Taiwan: A review	Tsai, CH; Chiu, HH; Abe, T
中國醫藥大學	2000	Aberrant transcripts of FHIT, TSG101 and PTEN/MMAC1 genes in normal peripheral mononuclear cells	Wang, NM; Chang, JG; Liu, TC; Lin, SF; Peng, CT; Tsai, FJ; Tsai, CH
中國醫藥大學	2000	G protein beta 3 subunit variant and essential hypertension in Taiwan - a case-control study	Tsai, CH; Yeh, HI; Chou, YS; Liu, HF; Yang, TY; Wang, JC; Wang, NM; Chang, JG
中國醫藥大學	2000	Analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency	Lee, HH; Chang, JG; Tsai, CH; Tsai, FJ; Chao, HT; Chung, BC
中國醫藥大學	2000	Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in cervical cancer	Su, TH; Chang, JG; Perng, LI; Chang, CP; Wei, HJ; Wang, NM; Tsai, CH
中國醫藥大學	2000	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
中國醫藥大學	2000	No evidence of correlation between mutation at codon 531 of src and the risk of colon cancer in Chinese	Wang, NM; Yeh, KT; Tsai, CH; Chen, SJ; Chang, JG
國立臺灣大學	1999-12	Immunogenicity and safety of standard-titer AIK-C measles vaccine in 9-month-old infants.	Tsai, HY; Huang, LM; Shih, YT; Chen, JM; Jiang, TM; Tsai, CH; Lee, CY
國立臺灣大學	1999-06	Long-term outcome studies of hyperactive children: literature review	Tsai, CH; Gau, SF
國立臺灣大學	1999	Changes in the mRNA levels of delayed rectifier potassium channels in human atrial fibrillation.	Lai, LP; Su, MJ; Lin, JL; Lin, FY; Tsai, CH; Chen, YS; Tseng, YZ; Lien, WP; Huang, SK.
國立臺灣大學	1999	Down-regulation of L-type calcium channel and sarcoplasmic reticular Ca(2+)-ATPase mRNA in human atrial fibrillation without significant change in the mRNA of ryanodine receptor, calsequestrin and phospholamban: an insight into the mechanism of atria	Lai, LP; Su, MJ; Lin, JL; Lin, FY; Tsai, CH; Chen, YS; Huang, SK; Tseng, YZ; Lien, WP.
國立臺灣大學	1999	Measurement of funny current (I(f)) channel mRNA in human atrial tissue: correlation with left atrial filling pressure and atrial fibrillation.	Lai, LP; Su, MJ; Lin, JL; Tsai, CH; Lin, FY; Chen, YS; Hwang, JJ; Huang, SK; Tseng, YZ; Lien, WP.
中國醫藥大學	1999	Echocardiographic (ECHO) flow pattern of patent ductus arteriosus (PDA): An indicator of indomethacin (Ind.) treatment in premature infants	Su, BH; Lin, HC; Peng, CT; Tsai, CH; Yeh, TF
中國醫藥大學	1999	The effects of early postnatal dexamethasone (D) therapy on the blood cell count in preterm infants	Peng, CT; Lin, HC; Lin, YJ; Tsai, CH; Yeh, TF
中國醫藥大學	1999	Mutations in the fibroblast growth factor receptor 3 (FGFR3) cause achondroplasia, hypochondroplasia, and thanatophoric dysplasia: Taiwanese data	Tsai, FJ; Tsai, CH; Chang, JG; Wu, JY
中國醫藥大學	1999	Identification of a common N540K mutation in 8/18 Taiwanese hypochondroplasia patients: further evidence for genetic heterogeneity	Tsai, FJ; Wu, JY; Tsai, CH; Chang, JG
中國醫藥大學	1999	Bcl 10 is not commonly mutated in multiple primary solid tumors.	Chang, JG; Lee, HH; Wang, NM; Yeh, KT; Tsai, FJ; Tsai, CH
中國醫藥大學	1999	A rapid and direct detection for the CYP21P/CYP21 chimeric gene in steroid 21-hydroxylase deficiency: an analysis for PCR dropout.	Lee, HH; Chang, JG; Tsai, CH; Chung, BC
中國醫藥大學	1999	Further characterization of Wilson disease in Taiwan: identification of two novel mutations and high correlation between haplotype and mutation.	Wu, JY; Tsai, FJ; Lee, CC; Chang, JG; Tsai, CH
中國醫藥大學	1999	Immunogenicity and safety of standard-titer AIK-C measles vaccine in nine-month-old infants	Tsai, HY; Huang, LM; Shih, YT; Chen, JM; Jiang, TM; Tsai, CH; Lee, CY
中國醫藥大學	1999	Echocardiographic flow pattern of patent ductus arteriosus: a guide to indomethacin treatment in premature infants	Su, BH; Peng, CT; Tsai, CH
中國醫藥大學	1999	Early dexamethasone therapy and blood cell count in preterm infants	Peng, CT; Lin, HC; Lin, YJ; Tsai, CH; Yeh, TF
中國醫藥大學	1999	Different race, different face: minor anomalies in Chinese newborn infants	Tsai, FJ; Tsai, CH; Peng, CT; Wu, JY; Lien, CH; Wang, TR
中國醫藥大學	1999	Kawasaki disease complicated by peripheral gangrene	Chang, JS; Lin, JS; Peng, CT; Tsai, CH
中國醫藥大學	1999	Prenatal diagnosis of thoracopelvic dysplasia - A case report	Hsieh, YY; Hsu, TY; Lee, CC; Chang, CC; Tsai, HD; Tsai, CH
中國醫藥大學	1999	Prenatal diagnosis of thoracopelvic dysplasia - A case report	Hsieh, YY; Hsu, TY; Lee, CC; Chang, CC; Tsai, HD; Tsai, CH
中國醫藥大學	1999	Twin vs. singleton pregnancy - Clinical characteristics and latency periods in preterm premature rupture of membranes	Hsieh, YY; Chang, CC; Tsai, HD; Yang, TC; Lee, CC; Tsai, CH
中國醫藥大學	1999	Twin vs. singleton pregnancy - Clinical characteristics and latency periods in preterm premature rupture of membranes	Hsieh, YY; Chang, CC; Tsai, HD; Yang, TC; Lee, CC; Tsai, CH
中國醫藥大學	1999	The prenatal diagnosis of Pierre-Robin sequence	Hsieh, YY; Chang, CC; Tsai, HD; Yang, TC; Lee, CC; Tsai, CH
中國醫藥大學	1999	The prenatal diagnosis of Pierre-Robin sequence	Hsieh, YY; Chang, CC; Tsai, HD; Yang, TC; Lee, CC; Tsai, CH
中國醫藥大學	1999	Prenatal diagnosis of dyssegmental dysplasia - A case report	Hsieh, YY; Chang, CC; Tsai, HD; Lee, CC; Tsai, FJ; Tsai, CH
中國醫藥大學	1999	Apoptosis in primary cutaneous amyloidosis	Chang, YT; Wong, CK; Chow, KC; Tsai, CH
中國醫藥大學	1999	Molecular characterization of secretor type alpha(1,2)-fucosyltransferase gene deficiency in the Philippine population	Peng, CT; Tsai, CH; Lin, TP; Perng, LI; Kao, MC; Yang, TY; Wang, NM; Liu, TC; Lin, SF; Chang, JG
中國醫藥大學	1999	Molecular characterization of secretor type alpha(1,2)-fucosyltransferase gene deficiency in the Philippine population	Peng, CT; Tsai, CH; Lin, TP; Perng, LI; Kao, MC; Yang, TY; Wang, NM; Liu, TC; Lin, SF; Chang, JG

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