Associations between UGT1A1 and SLCO1B1 polymorphisms and susceptibility to neonatal hyperbilirubinemia in Thai population

por Atasilp, Chalirmporn, Kanjanapipak, Janjira, Vichayaprasertkul, Jaratdao, Jinda, Pimonpan, Tiyasirichokchai, Rawiporn, Srisawasdi, Pornpen, Prempunpong, Chatchay, Chamnanphon, Monpat, Puangpetch, Apichaya, Vanwong, Natchaya, Klongthalay, Suwit, Jantararoungtong, Thawinee, Sukasem, Chonlaphat
Publicado 2022

Epidermolysis Bullosa With Congenital Absence of Skin: Congenital Corneal Cloudiness and Esophagogastric Obstruction Including Extended Genotypic Spectrum of PLEC, LAMC2, ITGB4 and...

por Pongmee, Pharuhad, Wittayakornrerk, Sanchawan, Lekwuttikarn, Ramrada, Pakdeeto, Sasikarn, Watcharakuldilok, Piangor, Prempunpong, Chatchay, Tim-Aroon, Thipwimol, Puttanapitak, Chawintee, Wattanasoontornsakul, Piyawan, Junhasavasdikul, Thitiporn, Wongkittichote, Parith, Noojarern, Saisuda, Wattanasirichaigoon, Duangrurdee
Publicado 2022

Prospective Research in Infants with Mild Encephalopathy (PRIME) Identified in the First Six Hours of Life: Neurodevelopmental Outcomes at 18-22 Months

por Chalak, Lina F, Nguyen, Kim-Anh, Prempunpong, Chatchay, Heyne, Roy, Thayyil, Sudhin, Shankaran, Seetha, Laptook, Abbot R, Rollins, Nancy, Pappas, Athina, Koclas, Louise, Shah, Birju, Montaldo, Paolo, Techasaensiri, Benyachalee, Sánchez, Pablo J, Sant’Anna, Guilherme
Publicado 2018

Variations in medical practice of retinopathy of prematurity among 8 Asian countries from an international survey

por Youn, Young-Ah, Kim, Sae Yun, Cho, Su Jin, Chang, Yun Sil, Miyake, Fuyu, Kusuda, Satoshi, Iskandar, Adhi Teguh Perma, Rohsiswatmo, Rinawati, Dewi, Rizalya, Chee, Seok Chiong, Neoh, Siew Hong, Imperial, Ma. Lourdes S., Velasco, Belen Amparo E., Quek, Bin Huey, Lin, Yuh-Jyh, Chang, Jui-Hsing, Nuntnarumit, Pracha, Ngerncham, Sopapan, Supapannachart, Sarayut, Ozawa, Yuri, Tomotaki, Seiichi, Prempunpong, Chatchay, Prempraphan, Pathaporn, Isayama, Tetsuya
Publicado 2023