Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Hui Pin Hsiao"'
Autor:
Yu-Wen Pan, Tsung-Ying Ou, Yen-Yin Chou, Pao-Lin Kuo, Hui-Pin Hsiao, Pao-Chin Chiu, Ju-Li Lin, Fu-Sung Lo, Chung-Hsing Wang, Peng-Chieh Chen, Meng-Che Tsai
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-11 (2024)
Abstract Background Syndromic ciliopathies are a group of congenital disorders characterized by broad clinical and genetic overlap, including obesity, visual problems, skeletal anomalies, mental retardation, and renal diseases. The hallmark of the pa
Externí odkaz:
https://doaj.org/article/73060ee9b5c9490996048dfd21858c78
Autor:
Rai-Hseng Hsu, Wei-De Lin, Mei-Chyn Chao, Hui-Pin Hsiao, Siew-Lee Wong, Pao-Chin Chiu, Shao-Yin Chu, Yu-Yuan Ke, Beng-Huat Lau, Yin-Hsiu Chien, Wuh-Liang Hwu, Fuu-Jen Tsai, Chung-Hsing Wang, Ni-Chung Lee
Publikováno v:
Journal of the Formosan Medical Association, Vol 118, Iss 1, Pp 142-147 (2019)
Background: Congenital generalized lipodystrophy (CGL) is a rare disorder characterized by scarce adipose tissue. This disease is distributed worldwide, but little is known about these patients in the Chinese population. Here, we delineate the phenot
Externí odkaz:
https://doaj.org/article/ebefc780d6ae484f93b3268cb1cbfd97
Autor:
Rajni Kant, Chung-Kuang Lu, Hien Minh Nguyen, Hui-Hua Hsiao, Chao-Ju Chen, Hui-Pin Hsiao, Kai-Jay Lin, Cheng-Chieh Fang, Chia-Hung Yen
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 129, Iss , Pp 110348- (2020)
Non-alcoholic fatty liver disease (NAFLD) is currently the most frequently occurring liver disorder in the world. However, a specific drug for the treatment of patients with NAFLD is not available. Therefore, the discovery of novel compounds for the
Externí odkaz:
https://doaj.org/article/f1f63c322aab4850a07f45febc737f07
Autor:
Hsiang-Yu Lin, Chung-Lin Lee, Yuan-Rong Tu, Ya-Hui Chang, Dau-Ming Niu, Chia-Ying Chang, Pao Chin Chiu, Yen-Yin Chou, Hui-Pin Hsiao, Meng-Che Tsai, Mei-Chyn Chao, Li-Ping Tsai, Chia-Feng Yang, Pen-Hua Su, Yu-Wen Pan, Chen-Hao Lee, Tzu-Hung Chu, Chih-Kuang Chuang, Shuan-Pei Lin
Publikováno v:
International Journal of Medical Sciences; 2024, Vol. 21 Issue 1, p8-18, 11p
Autor:
PEN-HUA SU, JU-SHAN YU, YU-ZHEN WU, YU-SHEN TSAI, FU-SUNG LO, JU-LI LIN, MEI-CHYN CHAO, CHIA-CHI HSU, YU-YUAN KE, PAO-CHIN CHIU, JO-CHING CHEN, YING-HUA HUANG, SHUAN-PEI LIN, YEN-YIN CHOU, WEI-HSIN TING, SHUO-YU WANG, CHIAO-FAN CHIU, YEN-CHUN HUANG, HUI-PIN HSIAO, CHAO-HSU LIN
Publikováno v:
In Vivo; Jan/Feb2024, Vol. 38 Issue 1, p341-350, 10p
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 30, Iss 8, Pp 383-389 (2014)
The thyrotropin-releasing hormone (TRH) test is useful for differentiating central and primary hypothyroidism, and is also valuable for diagnosing hypothyroidism. The threshold of the TRH test is usually set at 10–40 mIU/L. However, some experts ar
Externí odkaz:
https://doaj.org/article/c2f6095aa0ad4ff88ba5df9f615953f5
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 30, Iss 2, Pp 86-93 (2014)
Early detection and interventions for metabolic syndrome (MetS) are the most cost-effective methods for preventing many chronic diseases. There have been discordant findings in various countries due to different genetics and lifestyles. The goal of t
Externí odkaz:
https://doaj.org/article/ec3cde18b9dd49288878cc818fb490e8
Autor:
Hsiu-Hui Huang, Tai-Heng Chen, Hui-Pin Hsiao, Chia-Tsuan Huang, Cheng-Chu Wang, Ya-Huei Shiau, Mei-Chyn Chao
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 26, Iss 11, Pp 615-620 (2010)
Congenital generalized lipodystrophy (CGL) is a rare autosomal recessive disease that is characterized by a near-complete absence of adipose tissue from birth or early infancy. Mutations in the BSCL2 gene are known to result in CGL2, a more severe ph
Externí odkaz:
https://doaj.org/article/bb527d76cba4433cacb1b1ac453bc8ca
Autor:
Yi-Ching Lin, Mei-Lan Tsai, Hui-Pin Hsiao, Mei-Chyn Chao, Chih-Hsing Hung, Chang-Hung Kuo, Chung-Hsiang Li, Ming-Sheng Lee
Publikováno v:
Journal of Inflammation Research
Chang-Hung Kuo,1,2 Mei-Lan Tsai,3 Chung-Hsiang Li,2,4 Hui-Pin Hsiao,4 Mei-Chyn Chao,4 Ming-Sheng Lee,4 Yi-Ching Lin,5â 8 Chih-Hsing Hung3,4,9 1Ta-Kuo Clinic, Kaohsiung, Taiwan; 2Department of Pediatrics, Kaohsiung Municipal Ta-Tung Hospital, Kao
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6e83b185000a94983c904dc12cf57c1
https://www.dovepress.com/altered-pattern-of-macrophage-polarization-as-a-biomarker-for-severity-peer-reviewed-fulltext-article-JIR
https://www.dovepress.com/altered-pattern-of-macrophage-polarization-as-a-biomarker-for-severity-peer-reviewed-fulltext-article-JIR
Autor:
Sisca Fran, Meng Che Tsai, Hsiang-Yu Lin, Ya-Hui Chang, Chia-Ying Chang, Chung-Lin Lee, Li-Ping Tsai, Pao-Chin Chiu, Chih-Kuang Chuang, Yen Yin Chou, Tzu-Hung Chu, Yu-Wen Pan, Ru-Yi Tu, Chen-Hao Lee, Hui-Pin Hsiao, Chia-Feng Yang, Mei-Chyn Chao, Dau-Ming Niu, Pen-Hua Su, Shuan-Pei Lin
Publikováno v:
Journal of Personalized Medicine
Volume 11
Issue 11
Journal of Personalized Medicine, Vol 11, Iss 1197, p 1197 (2021)
Volume 11
Issue 11
Journal of Personalized Medicine, Vol 11, Iss 1197, p 1197 (2021)
Background: Silver–Russell syndrome (SRS) is a clinically and genetically heterogeneous disorder characterized by severe intrauterine growth retardation, poor postnatal growth, characteristic facial features, and body asymmetry. Hypomethylation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c76541632b787c98bd791d926e6cbe8e