1 |
Lee HJ, Moon HS, Lee ES, Kim SH, Sung JK, Lee BS, et al. A case of concomitant Gilbert's syndrome and hereditary spherocytosis. Korean J Hepatol 2010;16:321-4.
DOI
ScienceOn
|
2 |
Perrotta S, Gallagher PG, Mohandas N. Hereditary spherocytosis. Lancet 2008;372:1411-26.
DOI
ScienceOn
|
3 |
Bader-Meunier B, Gauthier F, Archambaud F, Cynober T, Miélot F, Dommergues JP, et al. Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis. Blood 2001;97:399-403.
DOI
ScienceOn
|
4 |
Iijima S, Ohzeki T, Maruo Y. Hereditary spherocytosis coexisting with UDP-glucuronosyltransferase deficiency highly suggestive of Crigler-Najjar syndrome type II. Yonsei Med J 2011;52:369-72.
DOI
ScienceOn
|
5 |
Sharma S, Vukelja SJ, Kadakia S. Gilbert's syndrome co-existing with and masking hereditary spherocytosis. Ann Hematol 1997;74:287-9.
DOI
ScienceOn
|
6 |
Garg PK, Kumar A, Teckchandani N, Hadke NS. Hereditary spherocytosis coexisting with Gilbert's syndrome: a diagnostic dilemma. Singapore Med J 2008;49:e308-9.
|
7 |
del Giudice EM, Perrotta S, Nobili B, Specchia C, d'Urzo G, Iolascon A. Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis. Blood 1999;94:2259-62.
|
8 |
Owens D, Evans J. Population studies on Gilbert's syndrome. J Med Genet 1975;12:152-6.
DOI
|
9 |
Fretzayas A, Moustaki M, Liapi O, Karpathios T. Gilbert syndrome. Eur J Pediatr 2012;171:11-5.
DOI
ScienceOn
|
10 |
Bolton-Maggs PH, Langer JC, Iolascon A, Tittensor P, King MJ; General Haematology Task Force of the British Committee for Standards in Haematology. Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update. Br J Haematol 2012;156:37-49.
DOI
ScienceOn
|
11 |
Muraca M, Fevery J. Influence of sex and sex steroids on bilirubin uridine diphosphate-glucuronosyltransferase activity of rat liver. Gastroenterology 1984;87:308-13.
|
12 |
Tamary H, Aviner S, Freud E, Miskin H, Krasnov T, Schwarz M, et al. High incidence of early cholelithiasis detected by ultrasonography in children and young adults with hereditary spherocytosis. J Pediatr Hematol Oncol 2003;25:952-4.
DOI
ScienceOn
|
13 |
Sieg A, Arab L, Schlierf G, Stiehl A, Kommerell B. Prevalence of Gilbert's syndrome in Germany. Dtsch Med Wochenschr 1987;112:1206-8.
DOI
|
14 |
Kim YH, Yeon JE, Jung GM, Kim HJ, Kim JS, Byun KS, et al. A study of polymorphism in UDP-glucuronosyltransferase 1 (UGT-1A1) promoter gene in Korean patients with Gilbert's syndrome. Taehan Kan Hakhoe Chi 2002;8:132-8.
|
15 |
Monaghan G, Ryan M, Seddon R, Hume R, Burchell B. Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome. Lancet 1996;347:578-81.
DOI
ScienceOn
|
16 |
Maruo Y, D'Addario C, Mori A, Iwai M, Takahashi H, Sato H, et al. Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome. Hum Genet 2004;115:525-6.
DOI
ScienceOn
|
17 |
Yamamoto K, Sato H, Fujiyama Y, Doida Y, Bamba T. Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II. Biochim Biophys Acta 1998;1406:267-73.
DOI
ScienceOn
|
18 |
Lim JW, Choi JH, Nam YH, Seo IS, Yoon SM, Koo MS. A case of congenital hemolytic anemia of unknown cause combined with Gilbert's syndrome. Korean J Hematol 2008;43:58-61.
DOI
ScienceOn
|
19 |
Lee MJ, Chang YH, Kang SH, Mun SK, Kim H, Han CJ, et al. A case of hereditary spherocytosis coexisting with Gilbert's syndrome. Korean J Gastroenterol 2013;61:166-9.
DOI
|
20 |
Hong YS, Jin JY, Lee WR. A case of Gilbert's syndrome with severe neonatal hyperbilirubinemia. J Korean Soc Neonatol 2010;17:266-9.
DOI
|