Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Birth Weight and UGT1A1[original query] |
---|
Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia. Gastroenterology 2002 Jul 123 (1): 127-33. Huang Ching-Shan, Chang Pi-Feng, Huang May-Jen, Chen En-Sung, Chen Wu-Char |
UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms vs. neonatal hyperbilirubinemia: is there an association? Pediatric research 2012 Aug 72 (2): 169-73. Alencastro de Azevedo Laura, Reverbel da Silveira Themis, Carvalho Clarissa Gutierrez, Martins de Castro Simone, Giugliani Roberto, Matte Ursu |
Identifying term breast-fed infants at risk of significant hyperbilirubinemia. Pediatric research 2013 Oct 74 (4): 408-12. Chang Pi-Feng, Lin Yu-Cheng, Liu Kevin, Yeh Shu-Jen, Ni Yen-Hsu |
Risk factors associated with unconjugated neonatal hyperbilirubinemia in Malaysian neonates. Journal of tropical pediatrics 2013 Aug 59 (4): 280-5. Wong Feiliang, Boo NemYun, Othman Aino |
Association of UGT1A1 variants and hyperbilirubinemia in breast-fed full-term Chinese infants. PloS one 2014 9 (8): e104251. Zhou Youyou, Wang San-nan, Li Hong, Zha Weifeng, Wang Xuli, Liu Yuanyuan, Sun Jian, Peng Qianqian, Li Shilin, Chen Ying, Jin |
Profiling of UGT1A16, UGT1A160, UGT1A193, and UGT1A128 Polymorphisms in Indonesian Neonates With Hyperbilirubinemia Using Multiplex PCR Sequencing. Frontiers in pediatrics 2019 8 7 328. Amandito Radhian, Rohsiswatmo Rinawati, Carolina Erica, Maulida Rizka, Kresnawati Windhi, Malik Amari |
UGT1A1*6 mutation associated with the occurrence and severity in infants with prolonged jaundice. Frontiers in pediatrics 2023 1 10 1080212. Yang Zhe, Lin Fen, Xu Jia-Xin, Yang Hui, Wu Yong-Hao, Chen Zi-Kai, Xie He, Huang Bin, Lin Wei-Hao, Wu Jian-Peng, Ma Yu-Bin, Li Jian-Dong, Yang Li- |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 29, 2024
- Content source: