|
|
???tair.name??? >
???browser.page.title.author???
|
"lo fu sung"???jsp.browse.items-by-author.description???
Showing items 1-10 of 10 (1 Page(s) Totally)
1
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 |
| 臺大學術典藏 |
2022-02-21T23:31:20Z |
Data Homogeneity Effect in Deep Learning-Based Prediction of Type 1 Diabetic Retinopathy
|
Lo, Jui En; Kang, Eugene Yu Chuan; YUN-NUNG CHEN; Hsieh, Yi Ting; Wang, Nan Kai; TA-CHING CHEN; Chen, Kuan Jen; Wu, Wei Chi; Hwang, Yih Shiou; Lo, Fu Sung; Lai, Chi Chun |
| 國立臺灣大學 |
2015 |
Moyamoya disease in two patients with Noonan-like syndrome with loose anagen hair
|
Lo, Fu-Sung; Wang, Chao-Jan; Wong, Mun-Ching; Lee, Ni-Chung; 李妮鍾 |
| 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 |
| 國立臺灣大學 |
2010 |
Cushing's Disease in Children: Report of Three Cases
|
許秉依; 童怡靖; 李正婷; 羅福松; 吳木榮; 蔡文友; 杜永光; HSU, PING-YI; TUNG, YI-CHING; LEE, CHENG-TING; LO, FU-SUNG; WU, MU-ZON; TSAI, WEN-YU; TU, YONG-KWANG |
| 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 |
| 國立臺灣大學 |
2004 |
Clinical Features of Type 1 Diabetic Children at Initial Diagnosis
|
羅福松; 楊敏慧; 張鑾英; 歐湧淳; 范揚灝; LO, FU-SUNG; YANG, MIN-HAI; CHANG, LUAN-YIN; OU, YUNG-CHUN; VAN, YANG-HAU |
| 國立成功大學 |
2003-02 |
Deletion of the C4-CYP21 repeat module leading to the formation of a chimeric CYP21P/CYP21 gene in a 9.3-kb fragment as a cause of steroid 21-hydroxylase deficiency
|
Lee, Hsien-Hsiung; Chang, Shwu-Fen; Lee, Yann-Jinn; Raskin, Salmo; Lin, Shio-Jean; Chao, Mei-Chyn; Lo, Fu-Sung; Lin, Ching-Yu |
| 高雄醫學大學 |
2003 |
Delection of the C4-CYP21 repeat module leading to the formation of a cause of steroid 21-hydroxylase deficiency.
|
趙美琴; Lee, Hsien-Hsiung;Chang, Shwu-Fen;Lee, Yann-Jinn;Raskin, Salmo;Lin, Shio-Jean;Chao, Mei-Chyn;Lo, Fu-Sung;Lin , and Ching-Yi |
Showing items 1-10 of 10 (1 Page(s) Totally)
1
View [10|25|50] records per page
|
