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Volumn 114, Issue 11, 2009, Pages 2360-2361

Iron excess treatable by copper supplementation in acquired aceruloplasminemia: A new form of secondary human iron overload?

Author keywords

[No Author keywords available]

Indexed keywords

CERULOPLASMIN; COPPER; CORTICOSTEROID; FERRITIN; HEMOGLOBIN; IRON; TRANSFERRIN;

EID: 70349569996     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2009-06-226175     Document Type: Letter
Times cited : (17)

References (10)
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    • Harris ZL, Klomp LW, Gitlin JD. Aceruloplasminemia: an inherited neurodegenerative disease with impairment of iron homeostasis. Am J Clin Nutr. 1998;67:972S-977S.
    • (1998) Am J Clin Nutr , vol.67
    • Harris, Z.L.1    Klomp, L.W.2    Gitlin, J.D.3
  • 2
    • 34250800318 scopus 로고    scopus 로고
    • Ferroxidase activity is required for the stability of cell surface ferroportin in cells expressing GPI-ceruloplasmin
    • DOI 10.1038/sj.emboj.7601735, PII 7601735
    • De Domenico I, Ward DM, di Patti MC, et al. Ferroxidase activity is required for the stability of cell surface ferroportin in cells expressing GPI-ceruloplasmin. EMBO J. 2007;26:2823-2831. (Pubitemid 46975784)
    • (2007) EMBO Journal , vol.26 , Issue.12 , pp. 2823-2831
    • De Domenico, I.1    Ward, D.M.2    Di Patti, M.C.B.3    Jeong, S.Y.4    David, S.5    Musci, G.6    Kaplan, J.7
  • 3
    • 0023240051 scopus 로고
    • Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration
    • Miyajima H, Nishimura Y, Mizoguchi K, Sakamoto M, Shimizu T, Honda N. Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration. Neurology. 1987;37:761-767. (Pubitemid 17064662)
    • (1987) Neurology , vol.37 , Issue.5 , pp. 761-767
    • Miyajima, H.1    Nishimura, Y.2    Mizoguchi, K.3
  • 5
    • 0037103195 scopus 로고    scopus 로고
    • Copper deficiency masquerading as myelodysplastic syndrome
    • DOI 10.1182/blood-2002-01-0256
    • Gregg XT, Reddy V, Prchal JT. Copper deficiency masquerading as myelodysplastic syndrome. Blood. 2002;100:1493-1495. (Pubitemid 34864311)
    • (2002) Blood , vol.100 , Issue.4 , pp. 1493-1495
    • Gregg, X.1    Reddy, V.2    Prchal, J.T.3
  • 6
    • 3242718536 scopus 로고    scopus 로고
    • Copper deficiency myelopathy produces a clinical picture like subacute combined degeneration
    • Kumar N, Gross JB Jr, Ahlskog JE. Copper deficiency myelopathy produces a clinical picture like subacute combined degeneration. Neurology. 2004;63:33-39. (Pubitemid 38943775)
    • (2004) Neurology , vol.63 , Issue.1 , pp. 33-39
    • Kumar, N.1    Gross Jr., J.B.2    Ahlskog, J.E.3
  • 8
    • 52449131277 scopus 로고    scopus 로고
    • Denture cream: An unusual source of excess zinc, leading to hypocupremia and neurologic disease
    • Nations SP, Boyer PJ, Love LA, et al. Denture cream: an unusual source of excess zinc, leading to hypocupremia and neurologic disease. Neurology. 2008;71:639-643.
    • (2008) Neurology , vol.71 , pp. 639-643
    • Nations, S.P.1    Boyer, P.J.2    Love, L.A.3
  • 9
    • 66549119902 scopus 로고    scopus 로고
    • Neutropenia in congenital nephrotic syndrome of the Finnish type: Role of urinary ceruloplasmin loss
    • Ulinski T, Aoun B, Toubiana J, Vitkevic R, Bensman A, Donadieu J. Neutropenia in congenital nephrotic syndrome of the Finnish type: role of urinary ceruloplasmin loss. Blood. 2009;113:4820-4821.
    • (2009) Blood , vol.113 , pp. 4820-4821
    • Ulinski, T.1    Aoun, B.2    Toubiana, J.3    Vitkevic, R.4    Bensman, A.5    Donadieu, J.6
  • 10
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    • The copper-iron connection: Hereditary aceruloplasminemia
    • Nittis T, Gitlin JD. The copper-iron connection: hereditary aceruloplasminemia. Semin Hematol. 2002;39:282-289.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.