UGT1A1 gene variants and clinical risk factors modulate hyperbilirubinemia risk in newborns-Reference-Cited by-同舟云学术

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

Published:2013-11-14 Issue:2 Volume:34 Page:120-124
ISSN:0743-8346
Container-title:Journal of Perinatology
language:en
Short-container-title:J Perinatol

Author:

Tiwari P K,Bhutada A,Agarwal R,Basu S,Raman R,Kumar A

Publisher

Springer Science and Business Media LLC

Subject

Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health

Link

http://www.nature.com/articles/jp2013140.pdf

Reference27 articles.

1. Bhutani VK, Johnson L, Sivieri EM . Predictive ability of a predischarge hour-specific serum bilirubin for subsequent significant hyperbiliru- binemia in healthy term and near-term newborns. Pediatrics 1999; 103: 6–14.

2. Kaplan M, Muraca M, Hammerman C, Rubaltelli FF, Vilei MT, Vreman HJ et al. Imbalance between production and conjugation of bilirubin: a fundamental concept in the mechanism of neonatal jaundice. Pediatrics 2002; 110: e47.

3. Huang MJ, Kua KE, Teng HC, Tang KS, Weng HW, Huang CS . Risk factors for severe hyperbilirubinemia in neonates. Pediatr Res 2004; 56: 682–689.

4. Watchko JF, Lin Z, Clark RH, Kelleher AS, Walker MW, Spitzer AR . Complex multifactorial nature of significant hyperbilirubinemia in neonates. Pediatrics 2009; 124: e868–e877.

5. Bosma PJ, Chowdhury JR, Bakker C, Gantla S, de Boer A, Oostra BA et al. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert’s syndrome. N Eng J Med 1995; 333: 1171–1175.

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