Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: Hyperbilirubinemia and Abo[original query] |
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Genetic polymorphisms in Thai neonates with hyperbilirubinemia. Acta paediatrica (Oslo, Norway : 1992) 2009 Jul 98 (7): 1106-10. Prachukthum Sariya, Nunnarumit Pracha, Pienvichit Paneeya, Chuansumrit Ampaiwan, Songdej Daunthida, Kajanachumpol Saowanee, Pakakasama Samart, Hongeng Surad |
Complex multifactorial nature of significant hyperbilirubinemia in neonates. Pediatrics 2009 Nov 124 (5): e868-77. Watchko Jon F, Lin Zhili, Clark Reese H, Kelleher Amy S, Walker M Whit, Spitzer Alan R, |
A causal relationship between UDP-glucuronosyltransferase 1A1 promoter polymorphism and idiopathic hyperbilirubinemia in Turkish newborns. The Turkish journal of pediatrics 0 52 (1): 28-34. Ergin Hacer, Bican Mevlüt, Atalay O Er |
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 |
UGT1A1 gene variants and clinical risk factors modulate hyperbilirubinemia risk in newborns. Journal of perinatology : official journal of the California Perinatal Association 2014 Feb 34 (2): 120-4. Tiwari P K, Bhutada A, Agarwal R, Basu S, Raman R, Kumar |
Relation between Neonatal Icter and Gilbert Syndrome in Gloucose-6-Phosphate Dehydrogenase Deficient Subjects. Journal of clinical and diagnostic research : JCDR 2014 Mar 8 (3): 63-5. Zahedpasha Yadollah, Ahmadpour Mousa, Niaki Haleh Akhavan, Alaee Ehs |
Risk assessment of gene variants for neonatal hyperbilirubinemia in Taiwan. BMC pediatrics 2016 16 (1): 144. Weng Yi-Hao, Chiu Ya-Wen, Cheng Shao-Wen, Yang Chun-Y |
The role of UGT1A1 promoter polymorphism and exon-1 mutations in neonatal jaundice. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2016 Nov 1-21. Halis Hülya, Ergin Hacer, Köseler Aylin, Atalay Erol Öm |
Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case-Control Study. BioMed research international 2018 2018 7803175. Zhou Jinfu, Yang Changyi, Zhu Wenbin, Chen Shuwei, Zeng Yinglin, Wang Jing, Zhao Hong, Chen Yao, Lin Fe |
Study of Gilbert's Syndrome-Associated UGT1A1 Polymorphism in Jaundiced Neonates of ABO Incompatibility Hemolysis Disease. American journal of perinatology 2019 May . Yu Yingfang, Du Lizhong, Chen An, Chen Lih |
UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China. BMC pediatrics 2021 06 21 (1): 259. Yang Hui, Lin Fen, Chen Zi-Kai, Zhang Lin, Xu Jia-Xin, Wu Yong-Hao, Gu Jing-Ying, Ma Yu-Bin, Li Jian-Dong, Yang Li- |
Clinical features and genetic variations of severe neonatal hyperbilirubinemia: Five case reports. World journal of clinical cases 2022 Jul 10 (20): 6999-7005. Lin Fen, Xu Jian-Xin, Wu Yong-Hao, Ma Yu-Bin, Yang Li- |
Clinical and genetic risk factors associated with neonatal severe hyperbilirubinemia: a case-control study based on the China Neonatal Genomes Project. Frontiers in genetics 2024 1 14 1292921. Xiao Wang, Tiantian Xiao, Jin Wang, Bingbing Wu, Huijun Wang, Yulan Lu, Yaqiong Wang, Bin Chen, Liyuan Hu, Yun Cao, Rong Zhang, Guoqiang Cheng, Laishuan Wang, Zhihua Li, Xinran Dong, Lin Yang, Wenhao Zh |
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- Page last updated:Apr 22, 2024
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