Zobrazeno 1 - 10
of 144
pro vyhledávání: '"Wen-hsiang Lin"'
Autor:
Wen-Hsiang Lin1 warren@isu.edu.tw, Chih-Chi Yu2 yusupergo@gmail.com, Hsin-Wei Fu3 hfu@isu.edu.tw, Yun-Shao Jao4 Js891506@gmail.com
Publikováno v:
International Journal of Organizational Innovation. Apr2024, Vol. 16 Issue 4, p145-157. 13p.
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 61, Iss 5, Pp 812-817 (2022)
Objective: Low molecular weight heparin (LMWH) has been given to reproductive-age women with various indications. This study aims to assess the benefits and risks of such use. Materials and methods: We retrospectively reviewed data (n = 204) between
Externí odkaz:
https://doaj.org/article/8e87915a1e1d41a39e7347aa8a5192d6
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 61, Iss 4, Pp 722-725 (2022)
Objective: The prenatal course of a rare case with fetal anemia caused by maternal anti-c alloimmunization was reported. Case report: A 39-year-old female with anti-c and anti-E antibodies against red cells had previously experienced a stillbirth. At
Externí odkaz:
https://doaj.org/article/894b62700eed4ba6b73655b7ce6c009c
Autor:
Caleb Liang, Wen-Hsiang Lin, Tai-Yuan Chang, Chi-Hong Chen, Chen-Wei Wu, Wen-Yeo Chen, Hsu-Chia Huang, Yen-Tung Lee
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract Body ownership concerns what it is like to feel a body part or a full body as mine, and has become a prominent area of study. We propose that there is a closely related type of bodily self-consciousness largely neglected by researchers—exp
Externí odkaz:
https://doaj.org/article/ab5c1fabcaf5421ba3c10d4c5c543817
Publikováno v:
Diagnostics, Vol 12, Iss 10, p 2267 (2022)
Background: Hemophilia A (HA) and B (HB) are X-linked recessive disorders that mainly affect males born from a mother carrier. Females are rarely affected but a number of mechanisms have been suggested in symptomatic females, such as skewed X-chromos
Externí odkaz:
https://doaj.org/article/b4e07914b6f640ff95b5805325d67a41
Publikováno v:
Diagnostics, Vol 12, Iss 7, p 1709 (2022)
Background: Beckwith–Wiedemann syndrome (BWS) is a phenotypically and genetically heterogeneous disorder associated with epigenetic/genetic aberrations on chromosome 11p15.4p15.5. There is no consensus criterion for prenatal diagnosis of BWS. Metho
Externí odkaz:
https://doaj.org/article/ca6e66eec8c14068a775772eab1b6785
Publikováno v:
IEEE Access, Vol 7, Pp 8713-8725 (2019)
This paper describes research toward a tracking system for locating persons indoor based on low-cost Bluetooth Low Energy (BLE) beacons. Wireless fingerprinting based on BLE beacons has emerged as an increasingly popular solution for fine-grained ind
Externí odkaz:
https://doaj.org/article/5a38ef42583c4189b83475567021a4e8
Autor:
Shin-Yu Lin, Chien-Nan Lee, Ai-Ying Peng, Ti-Jia Yuan, Dong-Jay Lee, Wen-Hsiang Lin, Gwo-Chin Ma, Ming Chen
Publikováno v:
Journal of the Formosan Medical Association, Vol 117, Iss 11, Pp 1027-1031 (2018)
We present a rare male fetus with karyotype of mosaic 45,X that comprises two types of aberrant Y chromosomes arising de novo (Yq12 deletion and isodicentric Yq11.22). Both types of the aberrant Y chromosomes lack the AZFc region which are expected t
Externí odkaz:
https://doaj.org/article/d7f52b725d4b4341bb8b83aa1a22928d
Autor:
Tien-Yu Yao, Wan-Ju Wu, Kim-Seng Law, Mei-Hui Lee, Shun-Ping Chang, Dong-Jay Lee, Wen-Hsiang Lin, Ming Chen, Gwo-Chin Ma
Publikováno v:
Diagnostics, Vol 11, Iss 8, p 1457 (2021)
This study examined the molecular characterization of a prenatal case with true fetal mosaicism of small supernumerary marker chromosome 16 (sSMC(16)). A 41-year-old female underwent amniocentesis at 19 weeks of gestation due to advanced maternal age
Externí odkaz:
https://doaj.org/article/a48e13df49d3414c957b957b39bd618c
Autor:
Chung-Er Huang, Gwo-Chin Ma, Hei-Jen Jou, Wen-Hsiang Lin, Dong-Jay Lee, Yi-Shing Lin, Norman A. Ginsberg, Hsin-Fu Chen, Frank Mau-Chung Chang, Ming Chen
Publikováno v:
Molecular Cytogenetics, Vol 10, Iss 1, Pp 1-11 (2017)
Abstract Background Noninvasive prenatal testing (NIPT) based on cell-free DNA in maternal circulation has been accepted worldwide by the clinical community since 2011 but limitations, such as maternal malignancy and fetoplacental mosaicism, preclude
Externí odkaz:
https://doaj.org/article/9e1f0dd2d3db4ec58fa451c9f2bf9553