Zobrazeno 1 - 10
of 58
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:
Jien-Wen Chien, Gwo-Chin Ma, Yu-Yuan Ke, Mei-Chyn Chao, Hsin-Ru Wu, Tung-Ming Chang, Ming Chen, Kuan-Jung Chen
Publikováno v:
Pediatrics and Neonatology, Vol 62, Iss 3, Pp 327-328 (2021)
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:
Shuan-Pei Lin, Yann Jang Chen, Pao Chin Chiu, Chia-Ying Chang, Huei Ching Chiu, Ju Li Lin, Tung Ming Chang, You Hsin Huang, Chih-Kuang Chuang, Hsiang-Yu Lin, Dau Ming Niu, Ru Yi Tu, Mei Chyn Chao, Fuu Jen Tsai, Yu Chia Kao, Wuh-Liang Hwu, Chung Lin Lee
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 8, Pp n/a-n/a (2019)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
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 Children
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
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
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
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 30(6)
BACKGROUND Central precocious puberty (CPP), predominant in girls, is defined by early development of secondary sexual characteristics driven by the early secretion of hypothalamic gonadotropin releasing hormone (GnRH) and subsequent gonadotropin. Re