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Browsing by Author Chayada Tangshewinsirikul

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Showing results 1 to 6 of 6
Issue DateTitleAuthor(s)
1-May-2018Case report of transient abnormal myelopoiesis in fetuses with down syndromeWirada Hansahiranwadee; Chayada Tangshewinsirikul; Panyu Panburana; Faculty of Medicine, Ramathibodi Hospital, Mahidol University
1-Jan-2019Effects of probiotic supplements on insulin resistance in gestational diabetes mellitus: A double-blind randomized controlled trialAthasit Kijmanawat; Panyu Panburana; Sirimon Reutrakul; Chayada Tangshewinsirikul; University of Illinois at Chicago; Faculty of Medicine, Ramathibodi Hospital, Mahidol University
1-Dec-2017Lupeol and stigmasterol suppress tumor angiogenesis and inhibit cholangiocarcinoma growth in mice via downregulation of tumor necrosis factor-aThaned Kangsamaksin; Supattra Chaithongyot; Chanida Wootthichairangsan; Rattanavinan Hanchaina; Chayada Tangshewinsirikul; Jisnuson Svasti; Mahidol University; Chulabhorn Research Institute
20-Sep-2019The p.(Pro170Leu) variant in NOG impairs noggin secretion and causes autosomal dominant congenital conductive hearing loss due to stapes ankylosisYilai Shu; Lijun Wang; Xiaoting Cheng; Chayada Tangshewinsirikul; Weili Shi; Yasheng Yuan; Zhiqiang Yan; Huawei Li; Jun Shen; Bing Chen; Weiguo Zou; School of Life Sciences Fudan University; Zhengzhou University; Brigham and Women's Hospital; Faculty of Medicine, Ramathibodi Hospital, Mahidol University; Fudan University; Harvard Medical School Center for Hereditary Deafness; Shanghai Institute for Biological Sciences Chinese Academy of Sciences
1-Jan-2020Successful pregnancy outcome in Herlyn-Werner-Wunderlich syndrome with pyocolpos: A case report and literature reviewChayada Tangshewinsirikul; Wirada Dulyaphat; Sanpon Diawtipsukon; Yada Tingthanatikul; Chonthicha Satirapod; Duangrurdee Wattanasirichaigoon; Faculty of Medicine, Ramathibodi Hospital, Mahidol University
1-Jan-2021A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicingYoel 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; American University of Beirut Medical Center; Massachusetts General Hospital; Partners HealthCare Personalized Medicine; NYU Grossman School of Medicine; University of Iowa; Rabin Medical Center Israel; Maine Medical Center; Faculty of Medicine, Ramathibodi Hospital, Mahidol University; Harvard Medical School Center for Hereditary Deafness; Tel Aviv University, Sackler Faculty of Medicine; The University of Manchester; University of Pennsylvania Perelman School of Medicine; Harvard Medical School; Broad Institute; Hadassah University Medical Centre; Dor Yeshorim; Dor Yeshorim