Zobrazeno 1 - 10
of 14 988
pro vyhledávání: '"Chih-An Chen"'
Autor:
Po-Sung Chen, Ju Lee, Hui-Ping Pan, Yuh-Jyh Lin, Yung-Chieh Lin, Yu-Shan Chang, Yen-Ju Chen, Chia-Liang Yen, Ching-Wei Lin, Chih-An Chen, Chi-Chang Shieh
Publikováno v:
Journal of Microbiology, Immunology and Infection, Vol 56, Iss 4, Pp 871-874 (2023)
From 2011, 37 children were referred to a hospital due to low levels of T cell receptor excision circles (TRECs) from newborn screening. Among them, three children were immunologically characterized and followed up to show that postnatal corticostero
Externí odkaz:
https://doaj.org/article/41b75d3fc9534a0da89ccd59f02f15bc
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
ObjectiveChildren of women with systemic lupus erythematosus (SLE) are at risk for childhood-onset SLE (cSLE). This study evaluated the incidence of early-onset cSLE and associated risk factors, including concomitant maternal and paternal autoimmune
Externí odkaz:
https://doaj.org/article/f12b3f7a2a0349c6bef9a1900106b810
Autor:
Chih-An Chen, Shiuh-Liang Hsu, Ching-Hsi Hsiao, David Hui-Kang Ma, Chi-Chin Sun, Hun-Ju Yu, Po-Chiung Fang, Ming-Tse Kuo
Publikováno v:
Annals of Clinical Microbiology and Antimicrobials, Vol 19, Iss 1, Pp 1-8 (2020)
Abstract Background Fungal keratitis (FK) has been shown to be a climate-sensitive disease. The differentiation between FK from bacterial keratitis (BK) was difficult. The purpose of this study was to compare the bacteriology and mycology between tro
Externí odkaz:
https://doaj.org/article/261e262c6fe740cc9a3b9eedbcd5c0be
Autor:
Yi-Chu Liao, Szu-Yu Wu, Ya-Fang Huang, Pei-Chi Lo, Tzu-Yi Chan, Chih-An Chen, Chun-Hsin Wu, Che-Chia Hsu, Chia-Liang Yen, Peng-Chieh Chen, Chi-Chang Shieh
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Immune-mediated arthritis is an important chronic inflammatory disease of joints causing debilitating morbidity in affected patients. The mechanisms underlying immune-mediated arthritis have been intensively investigated, however the cellular and mol
Externí odkaz:
https://doaj.org/article/eec2468f89ac411ebe6f35a6d350844b
Publikováno v:
PLoS ONE, Vol 15, Iss 5, p e0233564 (2020)
BACKGROUND:High myopia is a sight-threatening disease that causes axial length elongation and severe complications. Data on the benefits of posterior scleral reinforcement surgery in myopia control have been conflicting. The purpose of this study was
Externí odkaz:
https://doaj.org/article/e005133761cf427bac9067d3e4946250
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
Autor:
Chih-Ping Chen, Jian-Pei Huang, 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 922-926 (2024)
Objective: We present prenatal diagnosis of Jacobsen syndrome associated with a distal 11q deletion and a distal 8q duplication by chromosome microarray analysis (CMA) in a fetus with multiple congenital anomalies on fetal ultrasound. Case Report: A
Externí odkaz:
https://doaj.org/article/5003a87398b74acfbfd1d20f9dd33506