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Items: 1 to 20 of 104

1.

Complex multifactorial nature of significant hyperbilirubinemia in neonates.

Watchko JF, Lin Z, Clark RH, Kelleher AS, Walker MW, Spitzer AR; Pediatrix Hyperbilirubinemia Study Group..

Pediatrics. 2009 Nov;124(5):e868-77. doi: 10.1542/peds.2009-0460.

PMID:
19858149
2.

Exploring the genetic architecture of neonatal hyperbilirubinemia.

Watchko JF, Lin Z.

Semin Fetal Neonatal Med. 2010 Jun;15(3):169-75. doi: 10.1016/j.siny.2009.11.003. Review.

PMID:
20022574
3.

Genetic polymorphisms in Thai neonates with hyperbilirubinemia.

Prachukthum S, Nunnarumit P, Pienvichit P, Chuansumrit A, Songdej D, Kajanachumpol S, Pakakasama S, Hongeng S.

Acta Paediatr. 2009 Jul;98(7):1106-10. doi: 10.1111/j.1651-2227.2009.01275.x.

PMID:
19397531
4.

Risk factors associated with unconjugated neonatal hyperbilirubinemia in Malaysian neonates.

Wong F, Boo N, Othman A.

J Trop Pediatr. 2013 Aug;59(4):280-5. doi: 10.1093/tropej/fmt023.

PMID:
23640907
5.

Coexpression of gene polymorphisms involved in bilirubin production and metabolism.

Lin Z, Fontaine J, Watchko JF.

Pediatrics. 2008 Jul;122(1):e156-62. doi: 10.1542/peds.2007-3249.

PMID:
18558634
6.

UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms vs. neonatal hyperbilirubinemia: is there an association?

Alencastro de Azevedo L, Reverbel da Silveira T, Carvalho CG, Martins de Castro S, Giugliani R, Matte U.

Pediatr Res. 2012 Aug;72(2):169-73.

PMID:
22580719
7.

Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphisms.

Sato H, Uchida T, Toyota K, Nakamura T, Tamiya G, Kanno M, Hashimoto T, Watanabe M, Aoki K, Hayasaka K.

J Hum Genet. 2015 Jan;60(1):35-40. doi: 10.1038/jhg.2014.98.

PMID:
25391605
8.

Risk of hyperbilirubinemia in breast-fed infants.

Chang PF, Lin YC, Liu K, Yeh SJ, Ni YH.

J Pediatr. 2011 Oct;159(4):561-5. doi: 10.1016/j.jpeds.2011.03.042.

PMID:
21592495
9.

Genetic factors related to unconjugated hyperbilirubinemia amongst adults.

Huang CS, Huang MJ, Lin MS, Yang SS, Teng HC, Tang KS.

Pharmacogenet Genomics. 2005 Jan;15(1):43-50.

PMID:
15864125
10.

[Genetic factors in the occurrence of neonatal unconjugated hyperbilirubinemia].

Sun LL, Chen YS, Yu ZZ, Huang BX, Xu G, Ma DL, Li CG, Liu L, Liu XH.

Zhongguo Dang Dai Er Ke Za Zhi. 2012 Apr;14(4):256-9. Chinese.

11.

The impact of SLCO1B1 genetic polymorphisms on neonatal hyperbilirubinemia: a systematic review with meta-analysis.

Liu J, Long J, Zhang S, Fang X, Luo Y.

J Pediatr (Rio J). 2013 Sep-Oct;89(5):434-43. doi: 10.1016/j.jped.2013.01.008. Review.

12.

Multiple Genetic Modifiers of Bilirubin Metabolism Involvement in Significant Neonatal Hyperbilirubinemia in Patients of Chinese Descent.

Yang H, Wang Q, Zheng L, Lin M, Zheng XB, Lin F, Yang LY.

PLoS One. 2015 Jul 6;10(7):e0132034. doi: 10.1371/journal.pone.0132034.

13.

Identifying term breast-fed infants at risk of significant hyperbilirubinemia.

Chang PF, Lin YC, Liu K, Yeh SJ, Ni YH.

Pediatr Res. 2013 Oct;74(4):408-12. doi: 10.1038/pr.2013.120.

PMID:
23857295
14.

[OATP 1B1 T521C/A388G is an important polymorphism gene related to neonatal hyperbilirubinemia].

Zhang HX, Zhao X, Yang Z, Peng CY, Long R, Li GN, Li J, He ZK.

Zhonghua Er Ke Za Zhi. 2010 Sep;48(9):650-5. Chinese.

PMID:
21092521
15.

Polymorphic variants of SLCO1B1 in neonatal hyperbilirubinemia in China.

Liu J, Long J, Zhang S, Fang X, Luo Y.

Ital J Pediatr. 2013 Aug 12;39:49. doi: 10.1186/1824-7288-39-49.

16.

UGT1A1 gene polymorphisms in North Indian neonates presenting with unconjugated hyperbilirubinemia.

Agrawal SK, Kumar P, Rathi R, Sharma N, DAS R, Prasad R, Narang A.

Pediatr Res. 2009 Jun;65(6):675-80. doi: 10.1203/PDR.0b013e31819ed5de.

PMID:
19430380
17.

Neonatal hyperbilirubinemia in infants with G6PD c.563C > T Variant.

Moiz B, Nasir A, Khan SA, Kherani SA, Qadir M.

BMC Pediatr. 2012 Aug 20;12:126. doi: 10.1186/1471-2431-12-126.

18.

Risk factors for severe hyperbilirubinemia in neonates.

Huang MJ, Kua KE, Teng HC, Tang KS, Weng HW, Huang CS.

Pediatr Res. 2004 Nov;56(5):682-9.

PMID:
15319464
19.

Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia.

Huang CS, Chang PF, Huang MJ, Chen ES, Chen WC.

Gastroenterology. 2002 Jul;123(1):127-33.

PMID:
12105841
20.

Effects of statin treatments and polymorphisms in UGT1A1 and SLCO1B1 on serum bilirubin levels in Chinese patients with hypercholesterolaemia.

Hu M, Tomlinson B.

Atherosclerosis. 2012 Aug;223(2):427-32. doi: 10.1016/j.atherosclerosis.2012.06.002.

PMID:
22749334
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