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Results: 1 to 20 of 112

1.

Clinical and genetic risk factors for moderate hyperbilirubinemia in Brazilian newborn infants.

Mezzacappa MA, Facchini FP, Pinto AC, Cassone AE, Souza DS, Bezerra MA, Albuquerque DM, Saad ST, Costa FF.

J Perinatol. 2010 Dec;30(12):819-26. doi: 10.1038/jp.2010.48. Epub 2010 Apr 8.

PMID:
20376058
[PubMed - indexed for MEDLINE]
2.

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
[PubMed - indexed for MEDLINE]
3.

(TA)n UDP-glucuronosyltransferase 1A1 promoter polymorphism in Nigerian neonates.

Kaplan M, Slusher T, Renbaum P, Essiet DF, Pam S, Levy-Lahad E, Hammerman C.

Pediatr Res. 2008 Jan;63(1):109-11.

PMID:
18043502
[PubMed - indexed for MEDLINE]
4.

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. Epub 2009 Apr 21.

PMID:
19397531
[PubMed - indexed for MEDLINE]
5.

Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia.

Kaplan M, Renbaum P, Levy-Lahad E, Hammerman C, Lahad A, Beutler E.

Proc Natl Acad Sci U S A. 1997 Oct 28;94(22):12128-32.

PMID:
9342374
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

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. Epub 2013 May 2.

PMID:
23640907
[PubMed - indexed for MEDLINE]
7.

Homozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia.

Boo NY, Wong FL, Wang MK, Othman A.

Pediatr Int. 2009 Aug;51(4):488-93. doi: 10.1111/j.1442-200X.2008.02798.x.

PMID:
19674361
[PubMed - indexed for MEDLINE]
8.

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. Epub 2009 Oct 26.

PMID:
19858149
[PubMed - indexed for MEDLINE]
Free Article
9.

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.

PMID:
22906047
[PubMed - indexed for MEDLINE]
Free PMC Article
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.

PMID:
22537951
[PubMed - indexed for MEDLINE]
Free Article
11.

Heme oxygenase-1 gene variants and hyperbilirubinemia risk in North Indian newborns.

Tiwari PK, Sethi A, Basu S, Raman R, Kumar A.

Eur J Pediatr. 2013 Dec;172(12):1627-32. doi: 10.1007/s00431-013-2091-7. Epub 2013 Jul 23.

PMID:
23877636
[PubMed - indexed for MEDLINE]
12.

Clinical characteristics of G6PD deficiency in infants with marked hyperbilirubinemia.

Weng YH, Chiu YW.

J Pediatr Hematol Oncol. 2010 Jan;32(1):11-4. doi: 10.1097/MPH.0b013e3181c09aec.

PMID:
20051781
[PubMed - indexed for MEDLINE]
13.

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
[PubMed - indexed for MEDLINE]
14.

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
[PubMed - indexed for MEDLINE]
15.

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
[PubMed - indexed for MEDLINE]
16.

A causal relationship between UDP-glucuronosyltransferase 1A1 promoter polymorphism and idiopathic hyperbilirubinemia in Turkish newborns.

Ergin H, Bican M, Atalay OE.

Turk J Pediatr. 2010 Jan-Feb;52(1):28-34.

PMID:
20402064
[PubMed - indexed for MEDLINE]
Free Article
17.

Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G>A (G71R) mutation becomes a risk factor under inadequate feeding.

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

J Hum Genet. 2013 Jan;58(1):7-10. doi: 10.1038/jhg.2012.116. Epub 2012 Sep 27.

PMID:
23014115
[PubMed - indexed for MEDLINE]
18.

Should we screen newborns for glucose-6-phosphate dehydrogenase deficiency in the United States?

Watchko JF, Kaplan M, Stark AR, Stevenson DK, Bhutani VK.

J Perinatol. 2013 Jul;33(7):499-504. doi: 10.1038/jp.2013.14. Epub 2013 Feb 21. Review.

PMID:
23429543
[PubMed - indexed for MEDLINE]
19.

Glucose-6-phosphate dehydrogenase deficiency and borderline deficiency: association with neonatal hyperbilirubinemia.

Riskin A, Gery N, Kugelman A, Hemo M, Spevak I, Bader D.

J Pediatr. 2012 Aug;161(2):191-6.e1. doi: 10.1016/j.jpeds.2012.02.018. Epub 2012 Mar 27.

PMID:
22459229
[PubMed - indexed for MEDLINE]
20.

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. Epub 2009 Dec 21. Review.

PMID:
20022574
[PubMed - indexed for MEDLINE]

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