Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 131

1.

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]
2.

Prolonged unconjugated hyperbilirubinemia associated with breast milk and mutations of the bilirubin uridine diphosphate- glucuronosyltransferase gene.

Maruo Y, Nishizawa K, Sato H, Sawa H, Shimada M.

Pediatrics. 2000 Nov;106(5):E59.

PMID:
11061796
[PubMed - indexed for MEDLINE]
3.

211 G to a variation of UDP-glucuronosyl transferase 1A1 gene and neonatal breastfeeding jaundice.

Chou HC, Chen MH, Yang HI, Su YN, Hsieh WS, Chen CY, Chen HL, Chang MH, Tsao PN.

Pediatr Res. 2011 Feb;69(2):170-4. doi: 10.1203/PDR.0b013e31820263d2.

PMID:
20975617
[PubMed - indexed for MEDLINE]
4.

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. 2014 Nov 13. doi: 10.1038/jhg.2014.98. [Epub ahead of print]

PMID:
25391605
[PubMed - as supplied by publisher]
5.

Association between UGT 1A1 Gly71Arg (G71R) polymorphism and neonatal hyperbilirubinemia.

Prachukthum S, Gamnarai P, Kangsadalampai S.

J Med Assoc Thai. 2012 Jan;95 Suppl 1:S13-7.

PMID:
23964438
[PubMed - indexed for MEDLINE]
6.

Screening for G71R mutation of the UDP-glucuronosyltransferase 1 (UGT1A1) gene in neonates with pathologic and prolonged hyperbilirubinemia in Turkey.

Kilic I, Koseler A, Cakaloz I, Atalay E.

Int J Clin Pharmacol Ther. 2010 Aug;48(8):504-8.

PMID:
20650040
[PubMed - indexed for MEDLINE]
7.

Neonatal hyperbilirubinemia and G71R mutation of the UGT1A1 gene in Turkish patients.

Narter F, Can G, Ergen A, Isbir T, Ince Z, Çoban A.

J Matern Fetal Neonatal Med. 2011 Feb;24(2):313-6. doi: 10.3109/14767058.2010.490889. Epub 2010 Jun 8.

PMID:
20528217
[PubMed - indexed for MEDLINE]
8.

[Roles of UGT 1A1 gene mutation in the development of neonatal hyperbilirubinemia in Guangxi].

Gao ZY, Zhong DN, Liu Y, Liu YN, Wei LM.

Zhonghua Er Ke Za Zhi. 2010 Sep;48(9):646-9. Chinese.

PMID:
21092520
[PubMed - indexed for MEDLINE]
9.

Gly71Arg mutation of the bilirubin UDP-glucuronosyltransferase 1A1 gene is associated with neonatal hyperbilirubinemia in the Japanese population.

Yamamoto A, Nishio H, Waku S, Yokoyama N, Yonetani M, Uetani Y, Nakamura H.

Kobe J Med Sci. 2002 Aug;48(3-4):73-7.

PMID:
12502904
[PubMed - indexed for MEDLINE]
Free Article
10.

Development of icterus gravis in a preterm infant with G71R UGT1A1 polymorphism.

Kaga A, Ohkubo Y, Watanabe Y, Saito S, Matsuki T, Usuda H, Kanda S, Suzuki Y, Tanabu M, Kure S.

BMC Res Notes. 2013 Feb 6;6:51. doi: 10.1186/1756-0500-6-51.

PMID:
23388413
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism.

Maruo Y, Nishizawa K, Sato H, Doida Y, Shimada M.

Pediatrics. 1999 Jun;103(6 Pt 1):1224-7.

PMID:
10353933
[PubMed - indexed for MEDLINE]
12.

Neonatal hyperbilirubinemia and Gly71Arg mutation of UGT1A1 gene: a Chinese case-control study followed by systematic review of existing evidence.

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

Acta Paediatr. 2011 Jul;100(7):966-71. doi: 10.1111/j.1651-2227.2011.02176.x. Epub 2011 Feb 25. Review. Erratum in: Acta Paediatr. 2012 Nov;101(11):1184.

PMID:
21272068
[PubMed - indexed for MEDLINE]
13.

[Mutations in UGT1A1 gene in neonates with hyperbilirubinemia of Guangxi Heiyi Zhuang nationality].

Wu XJ, Zhong DN, Ye DZ, Zhong Y, Xie XZ.

Zhongguo Dang Dai Er Ke Za Zhi. 2014 May;16(5):483-8. Chinese.

PMID:
24856997
[PubMed - indexed for MEDLINE]
Free Article
14.

Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene: the common -3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese.

Kanai M, Kijima K, Shirahata E, Sasaki A, Akaba K, Umetsu K, Tezuka N, Kurachi H, Aikawa S, Hayasaka K.

Pediatr Int. 2005 Apr;47(2):137-41.

PMID:
15771689
[PubMed - indexed for MEDLINE]
15.

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]
16.

Bilirubin uridine diphosphate-glucuronosyltransferase variation is a genetic basis of breast milk jaundice.

Maruo Y, Morioka Y, Fujito H, Nakahara S, Yanagi T, Matsui K, Mori A, Sato H, Tukey RH, Takeuchi Y.

J Pediatr. 2014 Jul;165(1):36-41.e1. doi: 10.1016/j.jpeds.2014.01.060. Epub 2014 Mar 17.

PMID:
24650397
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Prolonged unconjugated hyperbiliriubinemia in breast-fed male infants with a mutation of uridine diphosphate-glucuronosyl transferase.

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

J Pediatr. 2009 Dec;155(6):860-3. doi: 10.1016/j.jpeds.2009.05.034. Epub 2009 Aug 14.

PMID:
19683255
[PubMed - indexed for MEDLINE]
18.

UGT1A1 haplotype mutation among Asians in Singapore.

Zhou YY, Lee LY, Ng SY, Hia CP, Low KT, Chong YS, Goh DL.

Neonatology. 2009;96(3):150-5. doi: 10.1159/000209851. Epub 2009 Mar 27.

PMID:
19325249
[PubMed - indexed for MEDLINE]
19.

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]
20.

Is breastfeeding really favoring early neonatal jaundice?

Bertini G, Dani C, Tronchin M, Rubaltelli FF.

Pediatrics. 2001 Mar;107(3):E41.

PMID:
11230622
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk