Zobrazeno 1 - 10
of 125
pro vyhledávání: '"Mei Chyn Chao"'
Autor:
Aman Bhakti Pulungan, Fabian Yap, Mei-Chyn Chao, Kah Yin Loke, Chen Yang, Tianrong Ma, Leroy Ovbude, Pen-Hua Su
Publikováno v:
Paediatrica Indonesiana, Vol 62, Iss 2, Pp 79-85 (2022)
Background Non-objective assessments indicate poor patient adherence to growth hormone (GH) prescribed for growth failure, with sub-optimal growth response. The easypod™ connect device for GH administration enables real-time, objective assessment o
Externí odkaz:
https://doaj.org/article/b6887653e95748d8a4f78587a681667b
Autor:
Hsiang-Yu Lin, Chung-Lin Lee, Chia-Ying Chang, Pao Chin Chiu, Yin-Hsiu Chien, Dau-Ming Niu, Fuu-Jen Tsai, Wuh-Liang Hwu, Shio Jean Lin, Ju-Li Lin, Mei-Chyn Chao, Tung-Ming Chang, Wen-Hui Tsai, Tzu-Jou Wang, Chih-Kuang Chuang, Shuan-Pei Lin
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Abstract Background Mucopolysaccharidoses (MPSs) are a group of inherited metabolic diseases, which are characterized by the accumulation of glycosaminoglycans, and eventually lead to the progressive damage of various tissues and organs. Methods An e
Externí odkaz:
https://doaj.org/article/1a7cb82677974c78a14f127068c04131
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:
Kuan-Jung Chen, Hsin-Ru Wu, Mei-Chyn Chao, Tung-Ming Chang, Jien-Wen Chien, Ming Chen, Gwo-Chin Ma, Yu-Yuan Ke
Publikováno v:
Pediatrics and Neonatology, Vol 62, Iss 3, Pp 327-328 (2021)
Externí odkaz:
https://doaj.org/article/1c5e63f0876a41c69b5c01da4c7fc7b6
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
Autor:
Chung‐Lin Lee, Hsiang‐Yu Lin, Chih‐Kuang Chuang, Huei‐Ching Chiu, Ru‐Yi Tu, You‐Hsin Huang, Wuh‐Liang Hwu, Fuu‐Jen Tsai, Pao‐Chin Chiu, Dau‐Ming Niu, Yann‐Jang Chen, Mei‐Chyn Chao, Tung‐Ming Chang, Ju‐Li Lin, Chia‐Ying Chang, Yu‐Chia Kao, Shuan‐Pei Lin
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 8, Pp n/a-n/a (2019)
Abstract Background Information on functional strengths and weaknesses of mucopolysaccharidosis (MPS) patients is important for early intervention programs and enzyme replacement therapy (ERT). Methods We used the Functional Independence Measure for
Externí odkaz:
https://doaj.org/article/f3646cc5c1dc4090a9d026a7f73a96bb
Autor:
Pen-Hua Su, Leroy Ovbude, Tianrong Ma, Chen Yang, Kah Yin Loke, Mei-Chyn Chao, Fabian Yap, Aman Bhakti Pulungan
Publikováno v:
Paediatrica Indonesiana. 62:79-85
Background Non-objective assessments indicate poor patient adherence to growth hormone (GH) prescribed for growth failure, with sub-optimal growth response. The easypod™ connect device for GH administration enables real-time, objective assessment o
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
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