Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 131

1.

A Case of hereditary spherocytosis coexisting with Gilbert's syndrome.

Lee MJ, Chang YH, Kang SH, Mun SK, Kim H, Han CJ, Kim J, Kang HJ.

Korean J Gastroenterol. 2013 Mar 25;61(3):166-9.

PMID:
23575236
[PubMed - indexed for MEDLINE]
Free Article
2.

A case of concomitant Gilbert's syndrome and hereditary spherocytosis.

Lee HJ, Moon HS, Lee ES, Kim SH, Sung JK, Lee BS, Jeong HY, Lee HY, Eu YJ.

Korean J Hepatol. 2010 Sep;16(3):321-4. doi: 10.3350/kjhep.2010.16.3.321.

PMID:
20924216
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Hereditary spherocytosis coexisting with Gilbert's syndrome: a diagnostic dilemma.

Garg PK, Kumar A, Teckchandani N, Hadke NS.

Singapore Med J. 2008 Nov;49(11):e308-9.

PMID:
19037536
[PubMed - indexed for MEDLINE]
Free Article
4.

Extreme hyperbilirubinemia in a patient with hereditary spherocytosis, Gilbert's syndrome, and obstructive jaundice.

Katz ME, Weinstein IM.

Am J Med Sci. 1978 May-Jun;275(3):373-9.

PMID:
686044
[PubMed - indexed for MEDLINE]
5.

[Gilbert's syndrome in patients with splenomegaly].

de Magalhães AF, Sevá-Pereira A.

Arq Gastroenterol. 1982 Oct-Dec;19(4):187-9. Portuguese.

PMID:
7186402
[PubMed - indexed for MEDLINE]
6.

Gilbert's syndrome co-existing with and masking hereditary spherocytosis.

Sharma S, Vukelja SJ, Kadakia S.

Ann Hematol. 1997 Jun;74(6):287-9.

PMID:
9236515
[PubMed - indexed for MEDLINE]
7.

Intractable neonatal jaundice due to hereditary spherocytosis and Gilbert's syndrome.

Ismail AQ, Gandhi A, El-Shimy N.

BMJ Case Rep. 2011 Jul 28;2011. pii: bcr0520114293. doi: 10.1136/bcr.05.2011.4293.

PMID:
22689841
[PubMed - indexed for MEDLINE]
Free PMC Article
8.
9.

Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis.

Kumar D, Parakh A, Sharma S.

J Pediatr Hematol Oncol. 2012 Jan;34(1):54-6. doi: 10.1097/MPH.0b013e318228fdd1.

PMID:
22134611
[PubMed - indexed for MEDLINE]
10.

Coexisting Gilbert's syndrome and sickle cell disease.

Borker A, Udall J, Warrier R.

South Med J. 2002 Aug;95(8):939-40.

PMID:
12190239
[PubMed - indexed for MEDLINE]
11.

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
[PubMed - indexed for MEDLINE]
12.

Gilbert's syndrome--a frequent cause of unconjugated hyperbilirubinemia in children after orthotopic liver transplantation.

Kathemann S, Lainka E, Baba HA, Hoyer PF, Gerner P.

Pediatr Transplant. 2012 Mar;16(2):201-4. doi: 10.1111/j.1399-3046.2012.01662.x.

PMID:
22360405
[PubMed - indexed for MEDLINE]
13.

Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome.

Monaghan G, Ryan M, Seddon R, Hume R, Burchell B.

Lancet. 1996 Mar 2;347(9001):578-81.

PMID:
8596320
[PubMed - indexed for MEDLINE]
14.

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
[PubMed - indexed for MEDLINE]
15.

Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis.

del Giudice EM, Perrotta S, Nobili B, Specchia C, d'Urzo G, Iolascon A.

Blood. 1999 Oct 1;94(7):2259-62.

PMID:
10498597
[PubMed - indexed for MEDLINE]
Free Article
16.

TATA-box mutant in the promoter of the uridine diphosphate glucuronosyltransferase gene in Italian patients with Gilbert's syndrome.

Sampietro M, Lupica L, Perrero L, Romano R, Molteni V, Fiorelli G.

Ital J Gastroenterol Hepatol. 1998 Apr;30(2):194-8.

PMID:
9675658
[PubMed - indexed for MEDLINE]
17.

Combined test for UGT1A1 -3279T-->G and A(TA)nTAA polymorphisms best predicts Gilbert's syndrome in Italian pediatric patients.

Ferraris A, D'Amato G, Nobili V, Torres B, Marcellini M, Dallapiccola B.

Genet Test. 2006 Summer;10(2):121-5.

PMID:
16792515
[PubMed - indexed for MEDLINE]
18.

[Gilbert's syndrome--myths and reality].

Muchová L, Kráslová I, Lenícek M, Vítek L.

Cas Lek Cesk. 2004;143(6):375-80. Review. Czech.

PMID:
15309863
[PubMed - indexed for MEDLINE]
19.

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.

PMID:
7565971
[PubMed - indexed for MEDLINE]
Free Article
20.

Molecular genetic basis of Gilbert's syndrome.

Burchell B, Hume R.

J Gastroenterol Hepatol. 1999 Oct;14(10):960-6. Review.

PMID:
10530490
[PubMed - indexed for MEDLINE]
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk