Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Mei‐Chyn Chao"'
Autor:
Mei Chyn Chao, Pao Chin Chiu, Siew Lee Wong, Fuu Jen Tsai, Wei De Lin, Ni-Chung Lee, Yu Yuan Ke, Hui Pin Hsiao, Wuh-Liang Hwu, Yin-Hsiu Chien, Chung Hsing Wang, Shao Yin Chu, Beng Huat Lau, Rai Hseng Hsu
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
Autor:
Yin-Hsiu Chien, Wen-Hui Tsai, Shio Jean Lin, Ju-Li Lin, Dau-Ming Niu, Chih-Kuang Chuang, Chung-Lin Lee, Wuh-Liang Hwu, Tzu-Jou Wang, Pao Chin Chiu, Fuu Jen Tsai, Shuan-Pei Lin, Hsiang-Yu Lin, Tung-Ming Chang, Mei-Chyn Chao, Chia-Ying Chang
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
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 epidemiolo
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 33(11)
Objectives Holocarboxylase synthetase deficiency (HCSD) (OMIM #253270) is a rare inborn error of metabolism with an estimated annual incidence of 1 in 200,000 people. Typical manifestations of HCSD include eczema, alopecia, lactic acidosis and hypera
Autor:
Wuh-Liang Hwu, Jiunn Ming Sheen, Mei Chyn Chao, Shinn Forng Peng, Yin-Hsiu Chien, Ni-Chung Lee, Chia-Tung Shun, Siew Lee Wong, Fuu Jen Tsai, Joseph Hang Leung
Publikováno v:
Blood Cells, Molecules, and Diseases. 53:105-109
Recombinant human acid β-glucosidase GBA (rhGBA) infusion is an effective therapy for non-neuropathic (type I) Gaucher disease (GD), but its effect on subacute neuropathic (type III) GD is still controversial. The most common genotype for type III G
Autor:
Dau Ming Niu, Huei Ching Chiu, Mei Chyn Chao, Ni-Chung Lee, Fuu Jen Tsai, Ru Yi Tu, Shuan-Pei Lin, Hsiang-Yu Lin, Yin-Hsiu Chien, Yen Yin Chou, You Hsin Huang, Chih-Kuang Chuang, Chung Lin Lee, Li Ping Tsai
Publikováno v:
American journal of medical genetics. Part A. 176(6)
Prader-Willi syndrome (PWS) is a genetic disorder with obesity, developmental delay, short stature, and behavioral abnormalities. The study aimed to assess the functional independence in children with PWS. The Functional Independence Measure for Chil
Autor:
Mei-Chyn Chao, Ching-Kuan Liu, Ming-Tsang Wu, Chi-Kung Ho, Eric K. Chen, Bai-Hsiun Chen, Jiunn-Ren Wu, Chia-Fang Wu
Publikováno v:
Environment International, Vol 44, Iss, Pp 75-79 (2012)
A major incident of phthalate-contaminated foodstuffs happened in Taiwan between April and July, 2011. Phthalates were deliberately added to foodstuffs as a substitute of emulsifier. We describe the course of this incident, government response and ma
Autor:
Hong-Ren Yu, Yu Wen Hsu, Ying Hsien Huang, Ho-Chang Kuo, Kuender D. Yang, Chih Lu Wang, Chi Di Liang, Mei Chyn Chao, Ming-Feng Hou, Ying Chi Lin, Wei Chiao Chang
Publikováno v:
The Scientific World Journal, Vol 2012 (2012)
The Scientific World Journal
The Scientific World Journal
Background. Kawasaki disease (KD) is characterized by systemic vasculitis of unknown etiology. Our previous studies showed expression ofCD40ligand on CD4+ T cells correlated to the coronary artery lesion (CAL) and disease progress in KD. Other studie
Autor:
Yoshihiro Onouchi, Wei Chiao Chen, Ying Hsien Huang, Yu Wen Hsu, Kuender D. Yang, Ho-Chang Kuo, Yung Shun Juan, Hong-Ren Yu, Jin Ding Huang, Chiu Ming Kuo, Jung San Huang, Wei Chiao Chang, Ya-Ling Yang, Mei Chyn Chao
Publikováno v:
Journal of Human Genetics. 56:840-845
Kawasaki disease (KD) is a systemic vasculitis associated with cardiovascular symptom. A previous study in the European descent has indicated that genetic variants of the transforming growth factor-β (TGF-β) pathway are involved in the KD susceptib
Autor:
Cheng-Chu Wang, Hsiu-Hui Huang, Chia-Tsuan Huang, Tai-Heng Chen, Ya-Huei Shiau, Hui-Pin Hsiao, 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
Autor:
Cheng Hung Huang, Pao Lin Kuo, Ming-Ren Chen, Mei-Chyn Chao, Jui-Lung Yen, Hsiang-Yu Lin, Li-Ping Tsai, Chi-Yu Huang, I-Ching Chou, Ju-Li Lin, Shuan-Pei Lin, Fuu Jen Tsai, Chih-Kuang Chuang, Pao-Ching Chiu
Publikováno v:
Journal of the Chinese Medical Association, Vol 71, Iss 6, Pp 305-309 (2008)
BackgroundInformation regarding the efficacy of growth hormone (GH) therapy in Asian Prader-Willi syndrome (PWS) patients is lacking. We report our experience with GH treatment in children with PWS in Taiwan.MethodsForty-six PWS patients (27 males, 1