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Items: 1 to 20 of 47

1.

Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three cases.

Jamwal M, Aggarwal A, Kumar V, Sharma P, Sachdeva MU, Bansal D, Malhotra P, Das R.

Clin Chim Acta. 2016 Jul 1;458:51-4. doi: 10.1016/j.cca.2016.04.020. Epub 2016 Apr 20.

PMID:
27108201
2.

Effectiveness of switching from oral ziprasidone to risperidone in a patient with comorbid autistic disorder, profound intellectual disability, Gilbert syndrome, and exacerbation of psychosis.

Del Casale A, Kotzalidis GD, Sacco M, Rapinesi C, De Giorgi R, Giardini M, D'Andreagiovanni M, Carlino N, Brugnoli R, Girardi P.

Psychiatr Danub. 2016 Mar;28(1):91-4. No abstract available.

3.

Donor Safety and Recipient Liver Function After Right-Lobe Liver Transplantation From Living Donors With Gilbert Syndrome.

Kang WH, Hwang S, Song GW, Jung DH, Kim KH, Park GC, Ha TY, Ahn CS, Moon DB, Yoon YI, Shin MH, Kim WJ, Kim SH, Lee SG.

Transplant Proc. 2015 Dec;47(10):2827-30. doi: 10.1016/j.transproceed.2015.10.050.

PMID:
26707296
4.

Scoliosis in a Patient With Gilbert Syndrome: A Case Report and Review of the Literature.

Li Z, Shen J, Liang J.

Medicine (Baltimore). 2015 Nov;94(47):e2147. doi: 10.1097/MD.0000000000002147.

5.

Evaluation of aortic stiffness in Gilbert syndrome patients: a protective effect of elevated bilirubin levels.

Yüce S, Cüre E, Çiçek Y, Cumhur Cüre M, Yılmaz A, Kızılkaya B.

Turk Kardiyol Dern Ars. 2015 Oct;43(7):599-606. doi: 10.5543/tkda.2015.44457.

6.

Protective effect of elevated bilirubin levels on cardiovascular disease in patients with Gilbert syndrome.

Gürel E, Tigen MK.

Turk Kardiyol Dern Ars. 2015 Oct;43(7):591-3. doi: 10.5543/tkda.2015.14868. No abstract available.

7.

Gilbert syndrome acts as a risk factor of developing gallstone among β hemoglobinopathy Tunisian patients.

Chaouch L, Kalai M, Chaouachi D, Mallouli F, Hafsia R, Ben Ammar S, Abbes S.

Tunis Med. 2015 Apr;93(4):237-41.

8.

Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome.

Maruo Y, Nakahara S, Yanagi T, Nomura A, Mimura Y, Matsui K, Sato H, Takeuchi Y.

J Gastroenterol Hepatol. 2016 Feb;31(2):403-8. doi: 10.1111/jgh.13071.

PMID:
26250421
9.

Unusual presentation of Gilbert disease with high levels of unconjugated bilirubin. Report of two cases.

Flores-Villalba E, Rodriguez-Montalvo C, Bosques-Padilla F, Arredondo-Saldaña G, Zertuche-Maldonado T, Torre-Flores L.

Rev Esp Enferm Dig. 2016 Apr;108(4):228-30. doi: 10.17235/reed.2015.3719/2015.

10.

Outcome and toxicities associated to chemotherapy in children with acute lymphoblastic leukemia and Gilbert syndrome. Usefulness of UGT1A1 mutational screening.

Berrueco R, Alonso-Saladrigues A, Martorell-Sampol L, Català-Temprano A, Ruiz-Llobet A, Toll T, Torrebadell M, Naudó M, Camós M, Rives S.

Pediatr Blood Cancer. 2015 Jul;62(7):1195-201. doi: 10.1002/pbc.25457. Epub 2015 Apr 8.

PMID:
25855413
11.

Perfluorocarbons and Gilbert syndrome (phenotype) in the C8 Health Study Population.

Fan H, Ducatman A, Zhang J.

Environ Res. 2014 Nov;135:70-5. doi: 10.1016/j.envres.2014.08.011. Epub 2014 Sep 28.

12.

Severe neonatal hyperbilirubinemia and UGT1A1 promoter polymorphism.

Travan L, Lega S, Crovella S, Montico M, Panontin E, Demarini S.

J Pediatr. 2014 Jul;165(1):42-5. doi: 10.1016/j.jpeds.2014.03.013. Epub 2014 Apr 14.

PMID:
24726540
13.

Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients.

Dabke PS, Colah RB, Ghosh KK, Nadkarni AH.

Hematology. 2014 Oct;19(7):388-92. doi: 10.1179/1607845413Y.0000000142. Epub 2013 Nov 30.

PMID:
24620945
14.

UGT1A1 gene mutations in Pakistani children suffering from inherited nonhemolytic unconjugated hyperbilirubinemias.

Khan S, Irfan M, Sher G, Zubaida B, Alvi MA, Yasinzai M, Naeem M.

Ann Hum Genet. 2013 Nov;77(6):482-7. doi: 10.1111/ahg.12039. Epub 2013 Aug 29.

15.

Anti-genotoxic potential of bilirubin in vivo: damage to DNA in hyperbilirubinemic human and animal models.

Wallner M, Antl N, Rittmannsberger B, Schreidl S, Najafi K, Müllner E, Mölzer C, Ferk F, Knasmüller S, Marculescu R, Doberer D, Poulsen HE, Vitek L, Bulmer AC, Wagner KH.

Cancer Prev Res (Phila). 2013 Oct;6(10):1056-63. doi: 10.1158/1940-6207.CAPR-13-0125. Epub 2013 Aug 27.

17.

Gallstone disease in Swedish twins is associated with the Gilbert variant of UGT1A1.

Marschall HU, Krawczyk M, Grünhage F, Katsika D, Einarsson C, Lammert F.

Liver Int. 2013 Jul;33(6):904-8. doi: 10.1111/liv.12141. Epub 2013 Mar 20.

PMID:
23517300
18.

Gilbert and Crigler Najjar syndromes: an update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database.

Canu G, Minucci A, Zuppi C, Capoluongo E.

Blood Cells Mol Dis. 2013 Apr;50(4):273-80. doi: 10.1016/j.bcmd.2013.01.003. Epub 2013 Feb 9.

PMID:
23403257
19.

Investigation of the aortic pulse wave velocity in patients with Gilbert's syndrome.

Arslan E, Çakar M, Şarlak H, Kılınç A, Demirbaş S, Ay SA, Karaman M, Bulucu F, Sağlam K.

Clin Exp Hypertens. 2013;35(7):512-5. doi: 10.3109/10641963.2012.758277. Epub 2013 Jan 3.

PMID:
23286369
20.

Wayward effect of polymorphism (TA)8 in the promoter region of UGT1A1 gene in a Mexican family.

Tintos-Hernández JA, Perea FJ, Ibarra B, Figuera LE.

West Indian Med J. 2012 Jan;61(1):81-3.

PMID:
22808571

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