Zobrazeno 1 - 10
of 14 857
pro vyhledávání: '"Chih An Chen"'
Autor:
Hung-Chieh Su, Yu-Chang Chang, Chih-Hao Chen, Meng-Yu Cheng, Wen-Hsin Hsih, Yi-Jhen Chen, Chia-Huei Chou, Yu-Chao Lin, Chiung-Tzu Hsiao, Hong-Mo Shih, Mao-Wang Ho, Po-Ren Hsueh
Publikováno v:
Journal of Microbiology, Immunology and Infection, Vol 57, Iss 6, Pp 868-878 (2024)
Background: The emergence of SARS-CoV-2 in late 2019 sparked the global COVID-19 pandemic, leading to varied vaccine policies worldwide. The evolving patterns of respiratory pathogens, aside from SARS-CoV-2, during the pandemic have had a significant
Externí odkaz:
https://doaj.org/article/b056c467c196406cba2f28ec8149ea92
Autor:
Chi-Ting Chung, Chih-Hao Chen, Yen-Heng Lin, Chang-Jie Cheng, Hai-Jui Chu, Chuan-Hsiu Fu, Kuo-Wei Chen, Chung-Wei Lee, Sung-Chun Tang, Jiann-Shing Jeng
Publikováno v:
Journal of the Formosan Medical Association, Vol 123, Iss 12, Pp 1253-1259 (2024)
Purpose: Carotid artery web (CaW) is a rare focal fibromuscular dysplasia that can lead to embolic strokes with large vessel occlusion. This condition can be effectively treated with endovascular thrombectomy (EVT). Our study aims to assess the preva
Externí odkaz:
https://doaj.org/article/542e97eb5923492f91e6ba50fb56b7e5
Autor:
Chun-Min Wang, Yu-Ming Chang, Ray-Chang Tzeng, Tsang-Shan Chen, Shang-Te Wu, Kuan-Hung Lin, Che-Chao Chang, Meng-Hua Huang, Si-Chon Vong, Mu-Han Wu, Chih-Hung Chen, Che-Wei Lin, Pi-Shan Sung
Publikováno v:
Journal of the Formosan Medical Association, Vol 123, Iss 12, Pp 1246-1252 (2024)
Background: Endovascular thrombectomy (EVT) is a time-sensitive treatment for acute ischemic stroke with large vessel occlusion. To optimize transfer efficiency, a web-based platform was introduced in the Tainan Stroke Network (TSN). We assessed its
Externí odkaz:
https://doaj.org/article/ba721510f5444884937659cb72dc20ab
Autor:
Fang-Tzu Wu, Chih-Ping Chen
Publikováno v:
Journal of Medical Ultrasound, Vol 32, Iss 4, Pp 285-290 (2024)
Amniotic fluid assessment is crucial in prenatal ultrasound to monitor fetal conditions, with polyhydramnios, characterized by excessive amniotic fluid, affecting 1%–2% of pregnancies. Polyhydramnios is linked to complications such as placental abr
Externí odkaz:
https://doaj.org/article/b5837cc18ae5430abb1e947cf2265275
Autor:
Yeong-Yuh Xu, Shao-Jen Weng, Ping-Wen Huang, Lee-Min Wang, Chih-Hao Chen, Yao-Te Tsai, Ming-Che Tsai
Publikováno v:
BMC Health Services Research, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Objective The number of patients using emergency medical services (EMS) through ambulance dispatch has been increasing annually in Taiwan. Due to limited medical resource allocation, patients may not get on-time admission after they are sent
Externí odkaz:
https://doaj.org/article/bb4fac08abaf4037b1d98245ed0768cd
Autor:
Yu-Ren Wang, Shao-Ming Chang, Jinn-Jy Lin, Hsiao-Chian Chen, Lo-Tung Lee, Dien-Yu Tsai, Shih-Da Lee, Chung-Yu Lan, Chuang-Rung Chang, Chih-Feng Chen, Chen Siang Ng
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-17 (2024)
Abstract Background Z-DNA, a left-handed helical form of DNA, plays a significant role in genomic stability and gene regulation. Its formation, associated with high GC content and repetitive sequences, is linked to genomic instability, potentially le
Externí odkaz:
https://doaj.org/article/9305d39835f84a798472f43287d23cb2
Autor:
Chih-Ping Chen, Chen-Yu Chen, Fang-Tzu Wu, Peih-Shan Wu, Yen-Ting Pan, Chen-Chi Lee, Wen-Lin Chen, Wayseen Wang
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 63, Iss 6, Pp 913-917 (2024)
Objective: We present prenatal diagnosis of a 14-Mb 11p11.2-p13 deletion by chromosome microarray analysis (CMA) in a pregnancy with fetal recombinant chromosome 11 syndrome of rec(11)del(11) (p11.2p13)ins(11) (q21p11.2p13) and maternal intrachromoso
Externí odkaz:
https://doaj.org/article/1f8948be708c4dcb8d40f60e4532930f
Autor:
Chih-Ping Chen, Shun-Long Weng, Fang-Tzu Wu, Peih-Shan Wu, Yen-Ting Pan, Wen-Lin Chen, Chien-Wen Yang, Wayseen Wang
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 63, Iss 6, Pp 909-912 (2024)
Objective: We present first-trimester application of expanded non-invasive prenatal testing (NIPT) in the genetic investigation of fetal 1p36 deletion syndrome associated with a familial unbalanced reciprocal translocation of 46,XX,der(1)t(1;2) (p36.
Externí odkaz:
https://doaj.org/article/08715fcd276149e3925dea0af7175041
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 63, Iss 6, Pp 931-934 (2024)
Objective: We present prenatal diagnosis of mosaic trisomy 21 at amniocentesis associated with unbalanced Robertsonian translocation in the fetus and a favorable fetal outcome. Case Report: A 41-year-old, primigravid woman underwent amniocentesis at
Externí odkaz:
https://doaj.org/article/65cf8a3ecaf54f3683ac337e53c9982f
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 63, Iss 6, Pp 918-921 (2024)
Objective: We present application of chromosome microarray analysis (CMA) in the detection of chromosome 5q interstitial deletion of 5q14.3-q31.1 in a second-trimester fetus with multiple congenital anomalies on fetal ultrasound. Case Report: A 30-ye
Externí odkaz:
https://doaj.org/article/42548832d7884df9b532af9d9df7a030