Risk factors for severe neonatal hyperbilirubinemia in low and middle-income countries: a systematic review and meta-analysis
BO Olusanya, FB Osibanjo, TM Slusher - PloS one, 2015 - journals.plos.org
Background Available evidence suggests that low-and middle-income countries (LMICs)
bear the greatest burden of severe neonatal hyperbilirubinemia characterized by …
bear the greatest burden of severe neonatal hyperbilirubinemia characterized by …
Roles of UGT1A1 Gly71Arg and TATA promoter polymorphisms in neonatal hyperbilirubinemia: A meta-analysis
J Wang, J Yin, M Xue, J Lyu, Y Wan - Gene, 2020 - Elsevier
Objective To identify the association between UGT1A1 Gly71Arg and TATA promoter
polymorphisms and neonatal hyperbilirubinemia. Methods The studies related to the …
polymorphisms and neonatal hyperbilirubinemia. Methods The studies related to the …
Prevalence, factors associated and treatment outcome of hyperbilirubinaemia in neonates admitted to St Francis hospital, Nsambya, Uganda: a descriptive study
C Nyangabyaki-Twesigye, E Mworozi, C Namisi… - African health …, 2020 - ajol.info
Background: With targeted management of neonatal hyperbilirubinaemia in high-income
countries, there has been a dras-tic drop in both the prevalence and mortality. On the …
countries, there has been a dras-tic drop in both the prevalence and mortality. On the …
Bilirubin enhances the activity of ASIC channels to exacerbate neurotoxicity in neonatal hyperbilirubinemia in mice
K Lai, XL Song, HS Shi, X Qi, CY Li, J Fang… - Science Translational …, 2020 - science.org
Neonatal hyperbilirubinemia is a common clinical condition that can lead to brain
encephalopathy, particularly when concurrent with acidosis due to infection, ischemia, and …
encephalopathy, particularly when concurrent with acidosis due to infection, ischemia, and …
The relationship between hyperbilirubinemia and the promoter region and first exon of UGT1A1 gene polymorphisms in Vietnamese newborns
TT Nguyen, W Zhao, X Yang, DN Zhong - Pediatric research, 2020 - nature.com
Background To investigate the relationship between unexplained indirect
hyperbilirubinemia of Vietnamese newborns and the polymorphism of the promoter TATA …
hyperbilirubinemia of Vietnamese newborns and the polymorphism of the promoter TATA …
Hyperbilirubinemia in preterm infants admitted to neonatal intensive care units in Ethiopia
S Aynalem, M Abayneh, G Metaferia… - Global Pediatric …, 2020 - journals.sagepub.com
Background. Hyperbilirubinemia is prevalent and protracted in preterm infants. This study
assessed the pattern of hyperbilirubinemia in preterm infants in Ethiopia. Methods. This …
assessed the pattern of hyperbilirubinemia in preterm infants in Ethiopia. Methods. This …
Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case‐Control Study
J Zhou, C Yang, W Zhu, S Chen, Y Zeng… - BioMed Research …, 2018 - Wiley Online Library
To date, the genetic risk factors for neonatal hyperbilirubinemia remain unknown in
Southeastern China. This case‐control study aimed to identify the genetic risk factors for …
Southeastern China. This case‐control study aimed to identify the genetic risk factors for …
Profiling of UGT1A1*6, UGT1A1*60, UGT1A1*93, and UGT1A1*28 Polymorphisms in Indonesian Neonates With Hyperbilirubinemia Using Multiplex PCR …
R Amandito, R Rohsiswatmo, E Carolina… - Frontiers in …, 2019 - frontiersin.org
Background: Single nucleotide polymorphism (SNP) variants of the uridine diphosphate
glucuronosyltransferase 1A1 (UGT1A1) gene have been studied as an important factor in …
glucuronosyltransferase 1A1 (UGT1A1) gene have been studied as an important factor in …
Effects of Gly71Arg mutation in UGT1A1 gene on neonatal hyperbilirubinemia: a systematic review and meta-analysis
Abstract Objective: The associations between Gly71Arg polymorphism in the coding region
of uridine diphosphate glucuronosyl transferase 1A1 (UGT1A1) gene and the risk of …
of uridine diphosphate glucuronosyl transferase 1A1 (UGT1A1) gene and the risk of …
[HTML][HTML] Association of neonatal hyperbilirubinemia with UGT1A1 gene polymorphisms: A meta-analysis
Z Yu, K Zhu, L Wang, Y Liu, J Sun - Medical science monitor …, 2015 - ncbi.nlm.nih.gov
Background The results of studies on association between the polymorphisms in the coding
region and the promoter of uridine diphosphateglucuronosyl transferase 1A1 (UGT1A1) and …
region and the promoter of uridine diphosphateglucuronosyl transferase 1A1 (UGT1A1) and …