| 國家衛生研究院 |
2012-01 |
Association of the ADRA1A gene and the severity of metabolic abnormalities in patients with schizophrenia
|
Cheng, C;Chiu, HJ;Loh, EW;Chan, CH;Hwu, TM;Liu, YR;Lan, TH |
| 國家衛生研究院 |
2024-04-08 |
Association of the AhR, ARNT, and AhRR gene polymorphisms and cord blood AhR levels with elevated cord blood IgE susceptibility in Taiwan mother-infant pairs: A nested case-control study
|
Lin, YC;Wang, LH;Wen, HJ;Yang, CY;Lee, YL;Lee, CC;Tsai, EM;Huang, SK;Guo, YLL |
| 國立成功大學 |
2024-12-01 |
Association of the AhR, ARNT, and AhRR gene polymorphisms and cord blood AhR levels with elevated cord blood IgE susceptibility in Taiwan mother-infant pairs: a nested case-control study
|
Lin;Ying-Chu;Wang;Li-Hsuan;Wen;Hui-Ju;Yang;Chiu-Yueh;Lee;Yung-Ling;Lee;Ching-Chang;Tsai;Eing-Mei;Huang;Shau-Ku;Guo, Leon;Yue-Liang |
| 國立成功大學 |
2024 |
Association of the AhR, ARNT, and AhRR gene polymorphisms and cord blood AhR levels with elevated cord blood IgE susceptibility in Taiwan mother-infant pairs: a nested case–control study
|
Lin;Y, -C.;Wang;L, -H.;Wen;H, -J.;Yang;C, -Y.;Lee;Y, -L.;Lee;C, -C.;Tsai;E, -M.;Huang;S, -K.;Guo, Leon;Y, -L. |
| 國立成功大學 |
2019-09 |
Association of the built environments and health-related quality of life in community-dwelling older adults: a cross-sectional study
|
Huang;Nuan-Ching;Chu;Cordia;Kung;Shiann-Far;Hu;Susan, C. |
| 國立成功大學 |
2019 |
Association of the built environments and health-related�quality of life in community-dwelling older adults: a cross-sectional study
|
Huang, N.-C.;Chu, Chu C.;Kung, S.-F.;Hu, S.C. |
| 中國醫藥大學 |
2011-01 |
Association of the C-285T and A5954G Polymorphisms in the DNA repair gene OGG1 with the Susceptibility of Rheumatoid Arthritis
|
陳世殷(Shih-Yin, Chen); 萬磊(Lei Wan); 黃春明(Chung-Ming Huang); 黃毓銓(Yu-Chuen Huang); 許晉銓(Jinn-Chyuan Sheu); 林應如(Ying-Ju Lin); 劉詩平(Shih-Ping Liu); 藍郁青(Yu-Ching Lan); 賴志和(Chih-HO Lai); 林振文(Lin Cheng Wen); 蔡長海(Chang-Hai Tsai); 蔡輔仁(Fuu-Jen Tsai)* |
| 國立臺灣大學 |
2005-12 |
Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases
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Lee, CN; Su, YN; Cheng, WF; Lin, MT; Wang, JK; Wu, MH; Hsieh, FJ |
| 國立臺灣大學 |
2005 |
ASSOCIATION OF THE C677T METHYLENETETRAHYDROFOLATE REDUCTASE MUTATION WITH CONGENITAL HEART DISEASES
|
李建南; 蘇怡寧; 鄭文芳; 林銘泰; 王主科; 吳美環; 李建南; 謝豐舟 |
| 臺大學術典藏 |
2020-02-06T05:22:29Z |
Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases
|
Hsieh F.-J.;Wu M.-H.;Wang J.-K.;Lin M.-T.;WEN-FANG CHENG;Su Y.-N.;Lee C.-N.; Lee C.-N.; Su Y.-N.; WEN-FANG CHENG; Lin M.-T.; Wang J.-K.; Wu M.-H.; Hsieh F.-J.; Lee C.-N.; Su Y.-N.; WEN-FANG CHENG; Lin M.-T.; Wang J.-K.; Wu M.-H.; Hsieh F.-J. |
| 臺大學術典藏 |
2020-02-12T04:06:26Z |
Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases
|
Hsieh F.-J.;Wu M.-H;Wang J.-K;Lin M.-T;Cheng W.-F;Su Y.-N;CHIEN-NAN LEE; CHIEN-NAN LEE; Su Y.-N; Cheng W.-F; Lin M.-T; Wang J.-K; Wu M.-H; Hsieh F.-J. |
| 臺大學術典藏 |
2020-02-14T02:50:12Z |
Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases
|
Lee C.-N.;Su Y.-N.;Wen-Fang Cheng;Lin M.-T.;Wang J.-K.;Wu M.-H.;Hsieh F.-J.; Lee C.-N.; Su Y.-N.; WEN-FANG CHENG; Lin M.-T.; Wang J.-K.; Wu M.-H.; Hsieh F.-J. |
| 臺大學術典藏 |
2020-12-21T02:55:25Z |
Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases
|
Lee C.-N.;Su Y.-N.;Cheng W.-F.;Ming-Tai Lin;Wang J.-K.;Wu M.-H.;Hsieh F.-J.; Lee C.-N.; Su Y.-N.; Cheng W.-F.; MING-TAI LIN; Wang J.-K.; Wu M.-H.; Hsieh F.-J. |
| 臺大學術典藏 |
2021-01-05T08:07:39Z |
Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases
|
Lee C.-N.;Su Y.-N.;Cheng W.-F.;Lin M.-T.;Wang J.-K.;Mei-Hwan Wu;Hsieh F.-J.; Lee C.-N.; Su Y.-N.; Cheng W.-F.; Lin M.-T.; Wang J.-K.; MEI-HWAN WU; Hsieh F.-J. |
| 臺大學術典藏 |
2021-01-06T05:46:48Z |
Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases
|
Lee C.-N.;Su Y.-N.;Cheng W.-F.;Lin M.-T.;Jou-Kou Wang;Wu M.-H.;Hsieh F.-J.; Lee C.-N.; Su Y.-N.; Cheng W.-F.; Lin M.-T.; JOU-KOU WANG; Wu M.-H.; Hsieh F.-J. |
| 臺大學術典藏 |
2021-02-04T06:05:12Z |
Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases
|
Chien-Nan Lee;Su Y.-N.;Cheng W.-F.;Lin M.-T.;Wang J.-K.;Wu M.-H.;Hsieh F.-J.; CHIEN-NAN LEE; Su Y.-N.; Cheng W.-F.; Lin M.-T.; Wang J.-K.; Wu M.-H.; Hsieh F.-J. |
| 中國醫藥大學 |
2013-01 |
Association of the C825T polymorphism in the GNB3 gene with obesity and metabolic phenotypes in a Taiwanese population
|
(Tun-Jen Hsiao);(Yuchi Hwang);(Can-Hong Liu);(Hua-Mei Chang);林詩鈞(Eugene Lin)* |
| 國立臺灣大學 |
2012 |
Association of the Congenital Neuromuscular Form of Glycogen Storage Disease Type IV With a Large Deletion and Recurrent Frameshift Mutation
|
Li, Sing-Chung; Hwu, Wuh-Liang; Lin, Ju-Li; Bali, Deeksha S.; Yang, Chen; Chu, Shih-Ming; Chien, Yin-Hsiu; Chou, Hung-Chieh; Chen, Chien-Yi; Hsieh, Wu-Shiun; Tsao, Po-Nien; Chen, Yuan-Tsong; Lee, Ni-Chung; 胡務亮; 謝武勳; 李妮鍾; 簡穎秀 |
| 臺大學術典藏 |
2020-12-09T01:38:32Z |
Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation
|
Li S.-C.; Hwu W.-L.; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; Chien Y.-H.; Chou H.-C.; Chen C.-Y.; Hsieh W.-S.; Tsao P.-N.; Chen Y.-T.; NI-CHUNG LEE |
| 臺大學術典藏 |
2020-12-16T02:25:38Z |
Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation
|
Li S.-C.; WUH-LIANG HWU; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; Chien Y.-H.; Chou H.-C.; Chen C.-Y.; Hsieh W.-S.; Tsao P.-N.; Chen Y.-T.; Lee N.-C. |
| 臺大學術典藏 |
2020-12-22T03:29:29Z |
Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation
|
Lee N.-C.; Li S.-C.; Hwu W.-L.; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; Chien Y.-H.; Chou H.-C.; Chen C.-Y.; Hsieh W.-S.; PO-NIEN TSAO; Chen Y.-T. |
| 臺大學術典藏 |
2020-12-24T02:03:54Z |
Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation
|
Lee N.-C.; Chen Y.-T.; Tsao P.-N.; Li S.-C.; Hwu W.-L.; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; Chien Y.-H.; HUNG-CHIEH CHOU; Chen C.-Y.; Hsieh W.-S. |
| 臺大學術典藏 |
2020-12-24T06:16:51Z |
Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation
|
Lee N.-C.; Chen Y.-T.; Tsao P.-N.; Hsieh W.-S.; Chen C.-Y.; Chou H.-C.; Li S.-C.; Hwu W.-L.; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; YIN-HSIU CHIEN |
| 臺大學術典藏 |
2021-01-21T02:05:00Z |
Association of the congenital neuromuscular form of glycogen storage disease type IV with a large deletion and recurrent frameshift mutation
|
Li S.-C.; Hwu W.-L.; Lin J.-L.; Bali D.S.; Yang C.; Chu S.-M.; Chien Y.-H.; Chou H.-C.; CHIEN-YI CHEN; Hsieh W.-S.; Tsao P.-N.; Chen Y.-T.; Lee N.-C. |
| 國立成功大學 |
2022 |
Association of the consumption of common drinks with early puberty in both sexes
|
Tsai, M.-C.;Lee, Y.L.;Chen, Y.C. |
