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Volumn 88, Issue 2, 2012, Pages 179-180

Letter to the editor

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE AMINOTRANSFERASE; ASPARTATE AMINOTRANSFERASE; CERULOPLASMIN; COPPER; CREATININE; TRIENTINE;

EID: 84855823497     PISSN: 09024441     EISSN: 16000609     Source Type: Journal    
DOI: 10.1111/j.1600-0609.2011.01711.x     Document Type: Letter
Times cited : (2)

References (11)
  • 1
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    • Was the C282Y mutation an Irish Gaelic mutation that the Vikings helped disseminate? HLA haplotype observations of hemochromatosis from the west coast of Sweden
    • Olsson KS, Konar J, Dufva IH, Ricksten A, Raha-Chowdhury R. Was the C282Y mutation an Irish Gaelic mutation that the Vikings helped disseminate? HLA haplotype observations of hemochromatosis from the west coast of Sweden. Eur J Haematol 2011;86:75-82.
    • (2011) Eur J Haematol , vol.86 , pp. 75-82
    • Olsson, K.S.1    Konar, J.2    Dufva, I.H.3    Ricksten, A.4    Raha-Chowdhury, R.5
  • 2
    • 0035139204 scopus 로고    scopus 로고
    • The Wilson's disease gene and phenotypic diversity
    • Riordan SM, Williams R. The Wilson's disease gene and phenotypic diversity. J Hepatol 2001;34:1615-71.
    • (2001) J Hepatol , vol.34 , pp. 1615-1671
    • Riordan, S.M.1    Williams, R.2
  • 3
    • 0346847502 scopus 로고    scopus 로고
    • Aceruloplasminemia, an iron metabolic disorder
    • Miyajima H. Aceruloplasminemia, an iron metabolic disorder. Neuropathology 2003;23:345-50.
    • (2003) Neuropathology , vol.23 , pp. 345-350
    • Miyajima, H.1
  • 4
    • 0034500466 scopus 로고    scopus 로고
    • Determination of the frequencies of ten allelic variants of the Wilson disease gene (ATP7B), in pooled DNA samples
    • Olsson C, Waldenström E, Westermark K, Landegren U, Syvänen AC. Determination of the frequencies of ten allelic variants of the Wilson disease gene (ATP7B), in pooled DNA samples. Eur J Hum Genet 2000;8:933-8.
    • (2000) Eur J Hum Genet , vol.8 , pp. 933-938
    • Olsson, C.1    Waldenström, E.2    Westermark, K.3    Landegren, U.4    Syvänen, A.C.5
  • 8
    • 0036905751 scopus 로고    scopus 로고
    • HFE gene mutations and iron metabolism in Wilson's disease
    • Erhardt A, Hoffmann A, Hefter H, Häussinger D. HFE gene mutations and iron metabolism in Wilson's disease. Liver 2002;22:474-8.
    • (2002) Liver , vol.22 , pp. 474-478
    • Erhardt, A.1    Hoffmann, A.2    Hefter, H.3    Häussinger, D.4
  • 9
    • 0032508265 scopus 로고    scopus 로고
    • Effect of treatment of Wilson's disease on natural history of haemochromatosis
    • Walshe JM, Cox DW. Effect of treatment of Wilson's disease on natural history of haemochromatosis. Lancet 1998;352:112-3.
    • (1998) Lancet , vol.352 , pp. 112-113
    • Walshe, J.M.1    Cox, D.W.2
  • 11
    • 38949162267 scopus 로고    scopus 로고
    • A rare case of hemochromatosis and Wilson's disease coexisting in the same patient
    • Abuzetun JY, Hazin R, Suker M, Porter J. A rare case of hemochromatosis and Wilson's disease coexisting in the same patient. J Natl Med Assoc 2008;100:112-4.
    • (2008) J Natl Med Assoc , vol.100 , pp. 112-114
    • Abuzetun, J.Y.1    Hazin, R.2    Suker, M.3    Porter, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.