Zobrazeno 1 - 10
of 22
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:
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:
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:
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:
Pei-Chin Lin, Yu-Wen Chen, Shih-Hsiung Lin, Zen-Kong Dai, Shah-Hwa Chou, Jiunn-Ren Wu, Twei-Shun Jaw, Mei-Chyn Chao, Tai-Tsung Chang
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 26, Iss 9, Pp 496-501 (2010)
Intrathoracic tumor is a rare entity in the pediatric population and neurogenic tumors account for 40-50% of childhood intrathoracic tumors. They can cause severe symptoms, such as respiratory distress, neurological dysfunction and metabolic disturba
Autor:
Yushin Tsai, Shuan-Pei Lin, Wuh-Liang Hwu, Ni-Chung Lee, Wei-De Lin, Chung Hsing Wang, Mei-Chyn Chao, I-Ching Chou, Fuu Jen Tsai
Publikováno v:
cclm. 48:485-488
Background: Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) is an autosomal dominant developmental disorder that includes an eyelid malformation associated with (type I) or without (type II) premature ovarian failure (POF). Mutations in
Autor:
Chang-Hung Kuo, I-Chen Chen, Zen-Kong Dai, Ming-Chen Paul Shih, Mei-Chyn Chao, Shih-Shiung Lin, Jiunn-Ren Wu
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 26, Iss 1, Pp 45-49 (2010)
Posttraumatic empyema is a rare complication of trauma with an incidence of 1.6–2.4% in trauma patients. However, it is rarely reported in children. We report the case of a 15-year-old boy who was involved in a traffic accident and diagnosed with a
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 25, Iss 11, Pp 588-595 (2009)
Recent longitudinal experiences have emphasized that the follow-up of children with treated congenital hypothyroidism (CHT) should not be limited to the cognitive domain. This study attempted to evaluate the emotional–behavioral profiles in childre
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