Case report of transient abnormal myelopoiesis in fetuses with down syndrome

by Wirada Hansahiranwadee, Chayada Tangshewinsirikul, Panyu Panburana
Published 2019

Factors influencing parental decisions to terminate pregnancies following prenatal diagnoses of major fetal anomalies at Ramathibodi Hospital, Bangkok, Thailand

by Papapin Pusayapaibul, Jittima Manonai, Chayada Tangshewinsirikul
Published 2022

Feasibility and learning curve of performing first trimester fetal anatomy screening among operators with varying experience using the protocol of the International Society of Ultr...

by Saranthorn Sripilaipong, Panyu Panburana, Rujira Wattanayingcharoenchai, Chayada Tangshewinsirikul
Published 2022

Effects of probiotic supplements on insulin resistance in gestational diabetes mellitus: A double-blind randomized controlled trial

by Athasit Kijmanawat, Panyu Panburana, Sirimon Reutrakul, Chayada Tangshewinsirikul
Published 2020

Effect of cord puncture site in cordocentesis at mid-pregnancy on pregnancy outcomes

by Chayada Tangshewinsirikul, Chanane Wanapirak, Wirawit Piyamongkol, Supatra Sirichotiyakul, Theera Tongsong
Published 2018

Lupeol and stigmasterol suppress tumor angiogenesis and inhibit cholangiocarcinoma growth in mice via downregulation of tumor necrosis factor-a

by Thaned Kangsamaksin, Supattra Chaithongyot, Chanida Wootthichairangsan, Rattanavinan Hanchaina, Chayada Tangshewinsirikul, Jisnuson Svasti
Published 2018

Successful pregnancy outcome in Herlyn-Werner-Wunderlich syndrome with pyocolpos: A case report and literature review

by Chayada Tangshewinsirikul, Wirada Dulyaphat, Sanpon Diawtipsukon, Yada Tingthanatikul, Chonthicha Satirapod, Duangrurdee Wattanasirichaigoon
Published 2020

Preeclampsia and Baby Complications Correlated to High-Risk Score for Obstructive Sleep Apnea Screen by STOP-Bang Questionnaire

by Lisa Sangkum, Saowanee Sawang, Visasiri Tantrakul, Chayada Tangshewinsirikul, Sukanya Siriyotha, Sivaporn Termpornlert, Rojnarin Komonhirun
Published 2022

The p.(Pro170Leu) variant in NOG impairs noggin secretion and causes autosomal dominant congenital conductive hearing loss due to stapes ankylosis

by Yilai Shu, Lijun Wang, Xiaoting Cheng, Chayada Tangshewinsirikul, Weili Shi, Yasheng Yuan, Zhiqiang Yan, Huawei Li, Jun Shen, Bing Chen, Weiguo Zou
Published 2020

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

by Yoel Hirsch, Chayada Tangshewinsirikul, Kevin T. Booth, Hela Azaiez, Devorah Yefet, Adina Quint, Tzvi Weiden, Zippora Brownstein, Michal Macarov, Bella Davidov, John Pappas, Rachel Rabin, Margaret A. Kenna, Andrea M. Oza, Katherine Lafferty, Sami S. Amr, Heidi L. Rehm, Diana L. Kolbe, Kathy Frees, Carla Nishimura, Minjie Luo, Chantal Farra, Cynthia C. Morton, Sholem Y. Scher, Josef Ekstein, Karen B. Avraham, Richard J.H. Smith, Jun Shen
Published 2022