Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Mei-Chyn Chao"'
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
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
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:
Chang-Hung Kuo, I-Chen Chen, Shih-Shiung Lin, Ming-Chen Paul Shih, Jiunn-Ren Wu, Zen-Kong Dai, Mei-Chyn Chao
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
Externí odkaz:
https://doaj.org/article/aced49263878455ca4bd2790611ef7c6
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
Externí odkaz:
https://doaj.org/article/439fda8bd843413d847ca95d9e181566
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 25, Iss 4, Pp 212-216 (2009)
A 15-year-old girl was admitted because of an acute onset of facial palsy and right hemiparesis. The patient had a history of moderate mental retardation and developmental delay. On admission, her vital signs were stable, except for high blood pressu
Externí odkaz:
https://doaj.org/article/014ef87c01844988a3fb2469478a4b96
Autor:
Hsiao-Lin Hwa, Yih-Yuan Chang, Chien-Hao Huang, Chung-Hsiung Chen, Yen-Shi Kao, Yuh-Jyh Jong, Mei-Chyn Chao, Tsang-Ming Ko
Publikováno v:
Journal of the Formosan Medical Association, Vol 107, Iss 6, Pp 463-469 (2008)
Duchenne/Becker muscular dystrophies are X-linked recessive disorders caused by mutations in the Duchenne muscular dystrophy (DMD) gene. We aimed to demonstrate the small mutation patterns of the DMD gene in Taiwanese subjects. Methods: We sequenced
Externí odkaz:
https://doaj.org/article/4de27393a122444482a9358022cb47b6
Autor:
Hsiao-Lin Hwa, Yih-Yuan Chang, Chung-Hsiung Chen, Yen-Shi Kao, Yuh-Jyh Jong, Mei-Chyn Chao, Tsang-Ming Ko
Publikováno v:
Journal of the Formosan Medical Association, Vol 106, Iss 5, Pp 339-346 (2007)
Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are X- linked recessive disorders caused by mutations in the DMD gene. We intended to determine the distribution of DMD gene deletions and duplications in local Taiwanese male pati
Externí odkaz:
https://doaj.org/article/95f31595fd49440c9089aafee0344fb8
Publikováno v:
Journal of the Formosan Medical Association, Vol 106, Iss 2, Pp 169-172 (2007)
Noonan syndrome (NS) is an autosomal dominant disorder presenting with characteristic facies, short stature, skeletal anomalies, and congenital heart defects. Mutations in protein-tyrosine phosphatase, nonreceptor-type 11 (PTPN11), encoding SHP-2, ac
Externí odkaz:
https://doaj.org/article/39102f58873140d8bbc8ec6eef9b84fa