메뉴 건너뛰기




Volumn 850, Issue , 1998, Pages 490-494

Nontransfusional iron overload in thalassemia: Association with hereditary hemochromatosis

Author keywords

[No Author keywords available]

Indexed keywords

FERRITIN; IRON; TRANSFERRIN;

EID: 0031849493     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.1998.tb10530.x     Document Type: Conference Paper
Times cited : (21)

References (15)
  • 1
    • 0001019873 scopus 로고
    • Primary iron overload
    • J. H. Brock, J. W. Halliday, M. J. Pippard & L.W. Powell, Eds. Saunders. London
    • POWELL, L. W. et al. 1994. Primary iron overload. In Iron Metabolism in Health and Disease. J. H. Brock, J. W. Halliday, M. J. Pippard & L.W. Powell, Eds.: 227-270. Saunders. London.
    • (1994) Iron Metabolism in Health and Disease , pp. 227-270
    • Powell, L.W.1
  • 2
    • 9344224529 scopus 로고    scopus 로고
    • A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
    • FEDER, J. N. et al. 1996. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nature Genet. 13: 399-408.
    • (1996) Nature Genet. , vol.13 , pp. 399-408
    • Feder, J.N.1
  • 3
    • 0030221927 scopus 로고    scopus 로고
    • Mutation analysis in hereditary hemochromatosis
    • BEUTLER, E. et al. 1996. Mutation analysis in hereditary hemochromatosis. Blood Cell, Mole., Dis. 22: 187-194.
    • (1996) Blood Cell, Mole., Dis. , vol.22 , pp. 187-194
    • Beutler, E.1
  • 4
    • 0030294028 scopus 로고    scopus 로고
    • Haemochromatosis and HLA-H
    • JAZWINSKA, E. C. et al. 1996. Haemochromatosis and HLA-H. Nature Genet. 14: 249-251.
    • (1996) Nature Genet. , vol.14 , pp. 249-251
    • Jazwinska, E.C.1
  • 5
    • 16144368650 scopus 로고    scopus 로고
    • Haemochromatosis and HLA-H
    • JOUANOLLE, A. M. et al. 1996. Haemochromatosis and HLA-H. Nature Genet. 14: 251-252.
    • (1996) Nature Genet. , vol.14 , pp. 251-252
    • Jouanolle, A.M.1
  • 6
    • 0030923653 scopus 로고    scopus 로고
    • Global prevalence of putative haemochromatosis mutations
    • MERRYWEATHER-CLARKE, A. T. et al. 1997. Global prevalence of putative haemochromatosis mutations. J. Med. Genet. 34: 275-278.
    • (1997) J. Med. Genet. , vol.34 , pp. 275-278
    • Merryweather-Clarke, A.T.1
  • 7
    • 0029827481 scopus 로고    scopus 로고
    • Clinical and biochemical abnormalities in people heterozygous for hemachromatosis
    • BULAJ, Z. J. et al. 1996. Clinical and biochemical abnormalities in people heterozygous for hemachromatosis. N. Eng. J. Med. 335: 1799-1805.
    • (1996) N. Eng. J. Med. , vol.335 , pp. 1799-1805
    • Bulaj, Z.J.1
  • 9
    • 0019510131 scopus 로고
    • Coincidental nontransfusional iron overload and thalassemia minor: Association with HLA-linked hemochromatosis
    • EDWARDS, C. Q. et al. 1981. Coincidental nontransfusional iron overload and thalassemia minor: association with HLA-linked hemochromatosis. Blood 58: 844-848.
    • (1981) Blood , vol.58 , pp. 844-848
    • Edwards, C.Q.1
  • 11
    • 0021303766 scopus 로고
    • Globin chain precipitation, deranged iron metabolism and dyserythropoiesis in some thalassaemia syndromes
    • WICKRAMASINGHE, S. N. et al. 1984. Globin chain precipitation, deranged iron metabolism and dyserythropoiesis in some thalassaemia syndromes. Haematologia 17: 35-55.
    • (1984) Haematologia , vol.17 , pp. 35-55
    • Wickramasinghe, S.N.1
  • 12
    • 0027202405 scopus 로고
    • β-thalassemia unlinked to the β-globin gene in an English family
    • THEIN, S. L. et al. 1993. β-thalassemia unlinked to the β-globin gene in an English family. Blood 82: 961-967.
    • (1993) Blood , vol.82 , pp. 961-967
    • Thein, S.L.1
  • 13
    • 0018614007 scopus 로고
    • Iron absorption and loading in β-thalassaemia intermedia
    • PIPPARD, M. J. et al. 1979. Iron absorption and loading in β-thalassaemia intermedia. Lancet 2: 819-821.
    • (1979) Lancet , vol.2 , pp. 819-821
    • Pippard, M.J.1
  • 14
    • 0030604479 scopus 로고    scopus 로고
    • Hereditary hemochromatosis
    • WITTE, D. L. et al. 1996. Hereditary hemochromatosis. Clin. Chim. Acta 245: 139-200.
    • (1996) Clin. Chim. Acta , vol.245 , pp. 139-200
    • Witte, D.L.1
  • 15
    • 0031016791 scopus 로고    scopus 로고
    • Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda
    • ROBERTS, A. G. et al. 1997. Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda. Lancet 349: 321-323.
    • (1997) Lancet , vol.349 , pp. 321-323
    • Roberts, A.G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.