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Volumn 88, Issue 2, 2003, Pages 220-222

Risk factors for hyperbilirubinemia and gallstones in Chinese patients with β thalassemia syndrome

Author keywords

Chinese; Gallstones; Gilbert alleles; Hyperbilirubinemia; Thalassemia

Indexed keywords

ADOLESCENT; ADULT; AGE; AGED; ARTICLE; BETA THALASSEMIA; BLOOD TRANSFUSION; CHILD; CHINESE; FEMALE; GALLSTONE; GENE FREQUENCY; GENOTYPE PHENOTYPE CORRELATION; GILBERT DISEASE; HUMAN; HYPERBILIRUBINEMIA; MAJOR CLINICAL STUDY; RISK ASSESSMENT; RISK FACTOR; ASIAN; CHINA; CHOLELITHIASIS; GENETICS; GENOTYPE; LETTER;

EID: 0037608696     PISSN: 03906078     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (13)

References (10)
  • 1
    • 0032852420 scopus 로고    scopus 로고
    • Co-inherited Gilbert's syndrome: A factor determining hyperbilirubinemia in homozygous α-thalassemia
    • Galanello R, Cipollina MD, Dessi C, Giagu N, Lai E, Cao A. Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinemia in homozygous α-thalassemia. Haematologica 1999;84:103-5.
    • (1999) Haematologica , vol.84 , pp. 103-105
    • Galanello, R.1    Cipollina, M.D.2    Dessi, C.3    Giagu, N.4    Lai, E.5    Cao, A.6
  • 2
    • 0035897912 scopus 로고    scopus 로고
    • Genetic determinants of jaundice and gallstones in haemoglobin E β thalassaemia
    • Premawardhena A, Fisher CA, Fathiu F, de Silva S, Perera W, Peto TE, et al. Genetic determinants of jaundice and gallstones in haemoglobin E β thalassaemia. Lancet 2001;357:1945-6.
    • (2001) Lancet , vol.357 , pp. 1945-1946
    • Premawardhena, A.1    Fisher, C.A.2    Fathiu, F.3    De Silva, S.4    Perera, W.5    Peto, T.E.6
  • 3
    • 0033816138 scopus 로고    scopus 로고
    • Variations of the bilirubin uridine-diphosphoglucuronosyl transferase 1A1 gene in healthy Taiwanese
    • Huang CS, Luo GA, Huang ML, Yu SC, Yang SS. Variations of the bilirubin uridine-diphosphoglucuronosyl transferase 1A1 gene in healthy Taiwanese. Pharmacogenetics 2000;10:539-44.
    • (2000) Pharmacogenetics , vol.10 , pp. 539-544
    • Huang, C.S.1    Luo, G.A.2    Huang, M.L.3    Yu, S.C.4    Yang, S.S.5
  • 6
    • 0030698230 scopus 로고    scopus 로고
    • Hyperbilirubinaemia in heterozygous β-thalassaemia is related to co-inherited Gilbert's syndrome
    • Galanello R, Perseu L, Melis MA, Cipollina L, Barella S, Giagu N, et al. Hyperbilirubinaemia in heterozygous β-thalassaemia is related to co-inherited Gilbert's syndrome. Br J Haematol 1997;99:433-6.
    • (1997) Br J Haematol , vol.99 , pp. 433-436
    • Galanello, R.1    Perseu, L.2    Melis, M.A.3    Cipollina, L.4    Barella, S.5    Giagu, N.6
  • 7
    • 0030663191 scopus 로고    scopus 로고
    • The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous β-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency
    • Sampietro M, Lupica L, Perrero L, Comino A, Martinez di Montemuros F, Cappellini MD, et al. The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous β-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency. Br J Haematol 1997;99:437-9.
    • (1997) Br J Haematol , vol.99 , pp. 437-439
    • Sampietro, M.1    Lupica, L.2    Perrero, L.3    Comino, A.4    Martinez di Montemuros, F.5    Cappellini, M.D.6
  • 8
    • 0008435402 scopus 로고    scopus 로고
    • 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. Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis. Blood 1999;94:2259-62.
    • (1999) Blood , vol.94 , pp. 2259-2262
    • Del Giudice, E.M.1    Perrotta, S.2    Nobili, B.3    Specchia, C.4    D'Urzo, G.5    Iolascon, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.