Literature DB >> 11883809

Presence of the genetic marker for Gilbert syndrome is associated with increased level and duration of neonatal jaundice.

N Roy-Chowdhury, B Deocharan, H R Bejjanki, J Roy-Chowdhury, C Koliopoulos, S Petmezaki, T Valaes.   

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Year:  2002        PMID: 11883809     DOI: 10.1080/080352502753458058

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


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  4 in total

1.  UGT1A1 gene mutations and neonatal hyperbilirubinemia in Guangxi Heiyi Zhuang and Han populations.

Authors:  Xiao-Jing Wu; Dan-Ni Zhong; Xiang-Zhi Xie; De-Zhi Ye; Zong-Yan Gao
Journal:  Pediatr Res       Date:  2015-07-22       Impact factor: 3.756

2.  UGT1A1 gene variants and clinical risk factors modulate hyperbilirubinemia risk in newborns.

Authors:  P K Tiwari; A Bhutada; R Agarwal; S Basu; R Raman; A Kumar
Journal:  J Perinatol       Date:  2013-11-14       Impact factor: 2.521

Review 3.  Inherited disorders of bilirubin clearance.

Authors:  Naureen Memon; Barry I Weinberger; Thomas Hegyi; Lauren M Aleksunes
Journal:  Pediatr Res       Date:  2015-11-23       Impact factor: 3.756

4.  Association of Neonatal Hyperbilirubinemia with UGT1A1 Gene Polymorphisms: A Meta-Analysis.

Authors:  Zibi Yu; Kaichang Zhu; Li Wang; Ying Liu; Jianmei Sun
Journal:  Med Sci Monit       Date:  2015-10-15
  4 in total

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