Zobrazeno 1 - 10
of 99
pro vyhledávání: '"Kuntharee, Traisrisilp"'
Autor:
Nitchanut Chaipongpun, Chanane Wanapirak, Supatra Sirichotiyakul, Fuanglada Tongprasert, Kasemsri Srisupundit, Suchaya Luewan, Kuntharee Traisrisilp, Phudit Jatavan, Sirinart Sirilert, Theera Tongsong
Publikováno v:
International Journal of Public Health, Vol 68 (2023)
Objective: To assess the effectiveness of Quad test in the detection of Down syndrome (DS) in routine practice among a large-scale population and to compare the effectiveness of Quad test based on the Western reference model (WM) and that based on Th
Externí odkaz:
https://doaj.org/article/c32c990ce30d49eead4f4a055ae35f32
Autor:
Kuntharee Traisrisilp, Supatra Sirichotiyakul, Fuanglada Tongprasert, Kasemsri Srisupundit, Suchaya Luewan, Phudit Jatavan, Sirinart Sirilert, Theera Tongsong
Publikováno v:
Clinical and Experimental Obstetrics & Gynecology, Vol 48, Iss 4, Pp 860-866 (2021)
Background: To determine the association between increased nuchal translucency (INT) and fetal outcomes among Thai population. Methods: A prospective database of fetal Down syndrome screening project was accessed to enable retrieval of the records of
Externí odkaz:
https://doaj.org/article/7957f246c0a0463b8951a07bbe9a34c0
Autor:
Kuntharee Traisrisilp, Supatra Sirichotiyakul, Fuanglada Tongprasert, Kasemsri Srisupundit, Suchaya Luewan, Phudit Jatavan, Sirinart Sirilert, Theera Tongsong
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 60, Iss 4, Pp 706-710 (2021)
Objective: To evaluate the performance of first trimester sonomarkers in the detection of fetal Down syndrome among Thai pregnant women. Materials and methods: Pregnant women at 11–13+6 weeks’ gestation underwent ultrasound examination for assess
Externí odkaz:
https://doaj.org/article/ec41967668f94bf9a2acddda8c6c0761
Autor:
Rakchanok Boonpiam, Chanane Wanapirak, Supatra Sirichotiyakul, Ratanaporn Sekararithi, Kuntharee Traisrisilp, Theera Tongsong
Publikováno v:
BMC Pregnancy and Childbirth, Vol 20, Iss 1, Pp 1-9 (2020)
Abstract Background To identify the relationship between quadruple test for aneuploidy screening (alpha-fetoprotein: AFP; free beta-human chorionic gonadotropin: b-hCG; unconjugated estriol: uE3 and inhibin-A: IHA) and fetal growth restriction and to
Externí odkaz:
https://doaj.org/article/ae0c896621704261901aaf154c20b560
Autor:
Kuntharee Traisrisilp, Fuanglada Tongprasert, Kasemsri Srisupundit, Suchaya Luewan, Theera Tongsong
Publikováno v:
Obstetrics & Gynecology Science, Vol 63, Iss 3, Pp 330-336 (2020)
Objective22q11.2DS (deletion syndrome) is one of the common serious anomalies resulting in high perinatal morbidity and mortality rate. Nevertheless, prenatal diagnosis of 22q11.2DS in Southeast Asia has never been described and its prevalence in pre
Externí odkaz:
https://doaj.org/article/6954ccc6103b40f997bcb3260549e4e6
Autor:
Fuanglada Tongprasert, Kasemsri Srisupundit, Suchaya Luewan, Kuntharee Traisrisilp, Phudit Jatavan, Theera Tongsong
Publikováno v:
Clinical Case Reports, Vol 10, Iss 2, Pp n/a-n/a (2022)
Abstract Simple assessment of FHR baseline variability can differentiate second‐degree heart block (SHB) from complete heart block (CHB). In cases of SHB, antepartum NST can be reliably used for fetal surveillance. Intrapartum assessment of FHR var
Externí odkaz:
https://doaj.org/article/8cf3451ad813426f93fd303f5c4ecc77
Autor:
Chanane Wanapirak, Wirawit Piyamongkol, Supatra Sirichotiyakul, Fuanglada Tongprasert, Kasemsri Srisupundit, Suchaya Luewan, Kuntharee Traisrisilp, Phudit Jatavan, Theera Tongsong
Publikováno v:
BMC Health Services Research, Vol 19, Iss 1, Pp 1-7 (2019)
Abstract Background To identify the performance of fetal Down syndrome (DS) screening for developing countries. Methods A prospective study on MSS (maternal serum screening) with complete follow-ups (n = 41,924) was conducted in 32 network hospitals
Externí odkaz:
https://doaj.org/article/df8f3f0110eb4b598ca4fa24ad9f3442
Publikováno v:
Clinical Case Reports, Vol 7, Iss 7, Pp 1365-1369 (2019)
Abstract In a difficult case of macroadenoma with progressive change during pregnancy, timely cesarean delivery, avoidance of breastfeeding, and intensive conservative treatment after birth could have satisfactory results, in terms of fetal outcomes,
Externí odkaz:
https://doaj.org/article/500bafc5b14a4022a71ce7dd38cf3d21
Publikováno v:
Diagnostics, Vol 12, Iss 4, p 885 (2022)
Ring chromosome 15, a rare genetic disease, is very rarely prenatally diagnosed. We present a unique case of fetal ring chromosome 15 with ultrasound findings at 32 weeks of gestation including congenital diaphragmatic hernia, hypoplasia of the aorta
Externí odkaz:
https://doaj.org/article/c3c404e8f3b1404a8a98c83af09ec93e
Publikováno v:
Diagnostics, Vol 12, Iss 2, p 421 (2022)
Cri-du-Chat syndrome (CdCS) is a rare but serious genetic disorder. Most cases occur de novo, without specific risk factors as an indication of invasive prenatal diagnosis. Moreover, no specific ultrasound findings have been reported to facilitate ea
Externí odkaz:
https://doaj.org/article/28414ae846d24544a019285beca848b5