|
|
Taiwan Academic Institutional Repository >
Browse by Author
|
"lee yann jinn"
Showing items 1-10 of 13 (2 Page(s) Totally)
1 2 > >>
View [10|25|50] records per page
| 臺大學術典藏 |
2022-09-21T23:33:22Z |
Use of expert consensus to improve the diagnosis and management of type 1 diabetes mellitus
|
Lin, Chia Hung; YI-CHING TUNG; TIEN-JYUN CHANG; Huang, Chien Ning; Hwu, Chii Min; Chen, Bai Hsiun; Chiu, Pao Chin; Chen, Jung Fu; Chen, Yann Jang; Chu, Der Ming; Huang, Bi Yu; Gung, Chang; Ke, Yu Yuan; Hsiao, Pi Jung; Kuo, Feng Chih; Lee, Ting I.; Lin, Ching Ling; Lee, Yann Jinn; Lo, Fu Sung; Ou, Horng Yih; Tai, Tong Yuan; Tsai, Meng Che; Tsai, Shih Tzer; Tu, Shih Te; Wang, Hui Fang; Wang, Jun Sing; Wong, Siew Lee; Wu, Yi Lei |
| 嘉南藥理大學 |
2014 |
Genetic Variations in the Kir6.2 Subunit (KCNJ11) of Pancreatic ATP-Sensitive Potassium Channel Gene Are Associated with Insulin Response to Glucose Loading and Early Onset of Type 2 Diabetes in Childhood and Adolescence in Taiwan
|
Jiang, Yi-Der; Chuang, Lee-Ming; Pei, Dee; Lee, Yann-Jinn; Wei, Jun-Nan; Sung, Fung-Chang; Chang, Tien-Jyun |
| 臺北醫學大學 |
2014 |
Human leucocyte antigen-G polymorphisms are associated with cervical squamous cell carcinoma risk in Taiwanese women
|
Yang, Yuh-Cheng;Chang, Tzu-Yang;Chen, Tze-Chien;Lin, Wen-Shan;Chang, Shih-Chuan;Lee, Yann-Jinn |
| 國立臺灣大學 |
2014 |
Mutations in Pseudohypoparathyroidism 1a and Pseudopseudohypoparathyroidism in Ethnic Chinese
|
Wu, Yi-Lei; Hwang, Daw-Yang; Hsiao, Hui-Pin; Ting, Wei-Hsin; Huang, Chi-Yu; Tsai, Wen-Yu; Chen, Hung-Chun; Chao, Mei-Chyn; Lo, Fu-Sung; Tsai, Jeng-Daw; Yang, Stone; Shih, Shin-Lin; Lin, Shuan-Pei; Lin, Chiung-Ling; Lee, Yann-Jinn; 蔡文友 |
| 臺北醫學大學 |
2012 |
Impact of pubertal development and physical activity on heart rate variability in overweight and obese children in Taiwan.
|
陳淑如; Chen, Su-Ru;Chiu, Hung-Wen;Lee, Yann-Jinn;Sheen, Tzong-Chi;Jeng, Chii |
| 國立成功大學 |
2008-04 |
Low frequency of the CYP21A2 deletion in ethnic Chinese (Taiwanese) patients with 21-hydroxylase deficiency
|
Lee, Hsien-Hsiung; Lee, Yann-Jinn; Wang, Yu-Mei; Chao, Hsiang-Tai; Niu, Dau-Ming; Chao, Mei-Chyn; Tsai, Fuu-Jen; Lo, Fu-Sung; Lin, Shio-Jean |
| 高雄醫學大學 |
2008 |
Low frequency of the CYP21A2 deletion in ethnic Chinese (Taiwanese) patients with 21-hydroxylase deficiency.
|
李賢雄;趙美琴; Lee, Hsien-Hsiung;Lee, Yann-Jinn;Wang, Yu-Mei;Chao, Hsiang-Tai;Niu, Dau-Ming;Chao, Mei-Chyn;Tsai, Fuu-Jen;Lo, Fu-Sung;Lin , Shio-Jean |
| 國立成功大學 |
2007-06 |
Prader-Willi syndrome in Taiwan
|
Lin, Hsiang-Yu; Lin, Shuan-Pei; Yen, Jui-Lung; Lee, Yann-Jinn; Huang, Chi-Yu; Hung, Han-Yang; Hsu, Chyong-Hsin; Kao, Hsin-An; Chang, Jui-Hsing; Chiu, Nan-Chang; Ho, Che-Sheng; Chao, Mei-Chyn; Niu, Dau-Ming; Tsai, Li-Ping; Kuo, Pao-Lin |
| 國立成功大學 |
2007-06 |
Genotype and phenotype in patients with Prader-Willi Syndrome in Taiwan
|
Lin, Hsiang-Yu; Lin, Shuan-Pei; Chuang, Chih-Kuang; Chen, Ming-Ren; Yen, Jui-Lung; Lee, Yann-Jinn; Huang, Chi-Yu; Tsai, Li-Ping; Niu, Dau-Ming; Chao, Mei-Chyn; Kuo, Pao-Lin |
| 高雄醫學大學 |
2007 |
Mutation al analysis of PTPN11 gene in Taiwanese children with Noonan syndrome.
|
趙美琴;羅福松; Hung, Chia-Sui;Lin, Ju-Li;Lee, Yann-Jinn;Lin, Shuan-Pei;Chao, Mei-Chyn;Lo , Fu-Sung |
Showing items 1-10 of 13 (2 Page(s) Totally)
1 2 > >>
View [10|25|50] records per page
|
