日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Asian Neonatal Network Collaboration (AsianNeo): a study protocol for international collaborative comparisons of health services and outcomes to improve quality of care for sick newborn infants in Asia - survey, cohort and quality improvement studies

亚洲新生儿网络协作(AsianNeo):一项旨在通过国际合作比较医疗服务和结果,以提高亚洲患病新生儿护理质量的研究方案——包括调查、队列研究和质量改进研究。

Isayama, Tetsuya; Miyake, Fuyu; Rohsiswatmo, Rinawati; Dewi, Rizalya; Ozawa, Yuri; Tomotaki, Seiichi; Morisaki, Naho; Chee, Seok Chiong; Neoh, Siew Hong; Imperial, Ma Lourdes S; Velasco, Belen Amparo E; Chang, Yun Sil; Cho, Su Jin; Youn, YoungAh; Quek, Bin Huey; Poon, Woei Bing; Amin, Zubair; Jayaratne, Kapila; Kumara, Saman; Lin, Yuh-Jyh; Chang, Jui-Hsing; Lin, Hsiang Yu; Lin, Ming-Chih; Nuntnarumit, Pracha; Ngerncham, Sopapan; Prempunpong, Chatchay; Prempraphan, Pathaporn; Supapannachart, Sarayut; Kusuda, Satoshi

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

一项国际调查显示,8个亚洲国家在早产儿视网膜病变的医疗实践方面存在差异。

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

Epidermolysis Bullosa With Congenital Absence of Skin: Congenital Corneal Cloudiness and Esophagogastric Obstruction Including Extended Genotypic Spectrum of PLEC, LAMC2, ITGB4 and COL7A1

先天性皮肤缺失伴大疱性表皮松解症:先天性角膜混浊和食管胃梗阻,包括PLEC、LAMC2、ITGB4和COL7A1基因型谱的扩展

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

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

UGT1A1 和 SLCO1B1 多态性与泰国人群新生儿高胆红素血症易感性的关系

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

Prospective research in infants with mild encephalopathy identified in the first six hours of life: neurodevelopmental outcomes at 18-22 months

针对出生后六小时内确诊的轻度脑病婴儿的前瞻性研究:18-22个月时的神经发育结果

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