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Volumn 60, Issue 5, 2003, Pages 737-741

Molecular diagnosis and prophylactic therapy for presymptomatic Chinese patients with Wilson disease

Author keywords

[No Author keywords available]

Indexed keywords

CERULOPLASMIN; COPPER; ZINC SULFATE;

EID: 0038326583     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.60.5.737     Document Type: Article
Times cited : (40)

References (16)
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    • (1995) The Metabolic Basis of Inherited Disease , pp. 2211-2235
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  • 3
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    • Prevention of Wilson's disease in asymptomatic patients
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    • (1968) N Engl J Med , vol.278 , pp. 352-359
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  • 4
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    • Development of neurologic symptoms in a patient with asymptomatic Wilson's disease treated with penicillamine
    • Brewer GJ, Turkay A, Yuzbaziyan-Gurkan V. Development of neurologic symptoms in a patient with asymptomatic Wilson's disease treated with penicillamine. Arch Neurol 1994;51:304-305.
    • (1994) Arch Neurol , vol.51 , pp. 304-305
    • Brewer, G.J.1    Turkay, A.2    Yuzbaziyan-Gurkan, V.3
  • 5
    • 0018764261 scopus 로고
    • Oral zinc sulphate as longterm treatment in Wilson's disease (hepatolenticular degeneration)
    • Hoogenraad TU, Koevoet R, de Ruyter Korver EGWM. Oral zinc sulphate as longterm treatment in Wilson's disease (hepatolenticular degeneration). Eur Neurol. 1979;18:205-211.
    • (1979) Eur Neurol , vol.18 , pp. 205-211
    • Hoogenraad, T.U.1    Koevoet, R.2    De Ruyter Korver, E.G.W.M.3
  • 7
    • 0034974763 scopus 로고    scopus 로고
    • Mutation analysis and the correlation between genotype and phenotype of Arg778Leu mutation in Chinese patients with Wilson disease
    • Wu Z-Y, Wang N, Lin M-T, Fang L, Murong S-X, Yu L. Mutation analysis and the correlation between genotype and phenotype of Arg778Leu mutation in Chinese patients with Wilson disease. Arch Neurol. 2001;58:971-976.
    • (2001) Arch Neurol , vol.58 , pp. 971-976
    • Wu, Z.-Y.1    Wang, N.2    Lin, M.-T.3    Fang, L.4    Murong, S.-X.5    Yu, L.6
  • 8
    • 0030202413 scopus 로고    scopus 로고
    • Gene diagnosis for hepatolenticular degeneration by genetic linkage analysis with four short tandem repeat polymorphisms
    • Wu Z-Y, Yu L, Wang N. Gene diagnosis for hepatolenticular degeneration by genetic linkage analysis with four short tandem repeat polymorphisms [in Chinese]. Zhonghua Yi Xue Za Zhi. 1996;76:578-581.
    • (1996) Zhonghua Yi Xue Za Zhi , vol.76 , pp. 578-581
    • Wu, Z.-Y.1    Yu, L.2    Wang, N.3
  • 9
    • 17544388130 scopus 로고    scopus 로고
    • Wilson's disease in patients presenting with liver disease: A diagnostic challenge
    • Steindl P, Ferenci P, Dienes HP, et al. Wilson's disease in patients presenting with liver disease: a diagnostic challenge. Gastroenterology. 1997;113:212-218.
    • (1997) Gastroenterology , vol.113 , pp. 212-218
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  • 10
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    • Uneven hepatic copper distribution in Wilson's disease
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    • Faa, G.1    Nurchi, V.2    Demelia, L.3
  • 11
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    • The Wilson disease is a putative copper transporting P-type ATPase similar to the Menkes gene
    • Bull O PC, Thomas GR, Rommens JM, Forbes JR, Cox DW. The Wilson disease is a putative copper transporting P-type ATPase similar to the Menkes gene. Nat Genet. 1993;5:327-337.
    • (1993) Nat Genet , vol.5 , pp. 327-337
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  • 12
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    • The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.