Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Mei-Chyn Chao"'
Autor:
Pei-Chin Lin, Shih-Hsiung Lin, Shah-Hwa Chou, Yu-Wen Chen, Tai-Tsung Chang, Jiunn-Ren Wu, Twei-Shun Jaw, Zen-Kong Dai, Mei-Chyn Chao
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
Externí odkaz:
https://doaj.org/article/a1fc45ca797d47f881d44a258d8238f3
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
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:
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
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
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:
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
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