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Items: 1 to 20 of 120

1.

Study of a family in the province of Matera presenting with glucose-6-phosphate dehydrogenase deficiency and Gilbert's syndrome.

Dell'edera D, Epifania AA, Tinelli A, Leo M, Novelli A, Di Trani A, Barrano G, Bertoli M, Mazzone E, Benedetto M, Simona D, Malvasi A.

Mol Med Rep. 2012 Jun;5(6):1521-5. doi: 10.3892/mmr.2012.830.

PMID:
22407023
2.

The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency.

Sampietro M, Lupica L, Perrero L, Comino A, Martinez di Montemuros F, Cappellini MD, Fiorelli G.

Br J Haematol. 1997 Nov;99(2):437-9.

PMID:
9375769
3.

Molecular pathogenesis of Gilbert's syndrome: decreased TATA-binding protein binding affinity of UGT1A1 gene promoter.

Hsieh TY, Shiu TY, Huang SM, Lin HH, Lee TC, Chen PJ, Chu HC, Chang WK, Jeng KS, Lai MM, Chao YC.

Pharmacogenet Genomics. 2007 Apr;17(4):229-36.

PMID:
17496722
4.

Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndrome.

Iolascon A, Faienza MF, Giordani L, Perrotta S, Ruggiu G, Meloni GF, del Giudice EM.

Eur J Haematol. 1999 May;62(5):307-10.

PMID:
10359058
6.

The combination of new missense mutation with [A(TA)7TAA] dinucleotide repeat in UGT1A1 gene promoter causes Gilbert's syndrome.

D'Angelo R, Rinaldi C, Donato L, Nicocia G, Sidoti A.

Ann Clin Lab Sci. 2015 Spring;45(2):202-5.

PMID:
25887876
7.

[A study of polymorphism in UDP-glucuronosyltransferase 1 (UGT-1A1) promoter gene in Korean patients with Gilbert's syndrome].

Kim YH, Yeon JE, Jung GM, Kim HJ, Kim JS, Byun KS, Bak YT, Lee CH.

Taehan Kan Hakhoe Chi. 2002 Jun;8(2):132-8. Korean.

8.

Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome.

Galanello R, Cipollina MD, Carboni G, Perseu L, Barella S, Corrias A, Cao A.

Eur J Pediatr. 1999 Nov;158(11):914-6.

PMID:
10541948
9.

(TA)8 allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndrome.

Iolascon A, Faienza MF, Centra M, Storelli S, Zelante L, Savoia A.

Haematologica. 1999 Feb;84(2):106-9.

10.
11.

Gilbert's syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonates.

Iolascon A, Faienza MF, Perrotta S, Meloni GF, Ruggiu G, del Giudice EM.

Haematologica. 1999 Feb;84(2):99-102.

12.

Rapid molecular diagnosis of the Gilbert's syndrome-associated exon 1 mutation within the UGT1A1 gene.

Hsieh TY, Shiu TY, Chu NF, Chao TY, Chu HC, Chang WK, Chao YC, Huang HH.

Genet Mol Res. 2014 Jan 28;13(1):670-9. doi: 10.4238/2014.January.28.12.

13.
14.

The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.

Bosma PJ, Chowdhury JR, Bakker C, Gantla S, de Boer A, Oostra BA, Lindhout D, Tytgat GN, Jansen PL, Oude Elferink RP, et al.

N Engl J Med. 1995 Nov 2;333(18):1171-5.

15.

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.

16.

Donor liver uridine diphosphate (UDP)-glucuronosyltransferase-1A1 deficiency causing Gilbert's syndrome in liver transplant recipients.

Te HS, Schiano TD, Das S, Kuan SF, DasGupta K, Conjeevaram HS, Baker AL.

Transplantation. 2000 May 15;69(9):1882-6.

PMID:
10830226
17.
18.

A homozygous mutation in UGT1A1 exon 5 may be responsible for persistent hyperbilirubinemia in a Japanese girl with Gilbert's syndrome.

Nakagawa T, Mure T, Yusoff S, Ono E, Kusuma Harahap IS, Morikawa S, Morioka I, Takeshima Y, Nishio H, Matsuo M.

Kobe J Med Sci. 2011 Jul 20;57(1):E26-31.

19.

Gilbert's syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn.

Monaghan G, McLellan A, McGeehan A, Li Volti S, Mollica F, Salemi I, Din Z, Cassidy A, Hume R, Burchell B.

J Pediatr. 1999 Apr;134(4):441-6.

PMID:
10190918
20.

Gilbert's disease and atazanavir: from phenotype to UDP-glucuronosyltransferase haplotype.

Lankisch TO, Moebius U, Wehmeier M, Behrens G, Manns MP, Schmidt RE, Strassburg CP.

Hepatology. 2006 Nov;44(5):1324-32.

PMID:
17058217

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