-
1
-
-
0031981976
-
Aceruloplasminemia: An inherited neurodegenerative disease with impairment of iron homeostasis
-
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
-
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
-
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
-
4
-
-
0036623360
-
Aceruloplasminemia: New clinical, pathophysiological and therapeutic insights
-
DOI 10.1016/S0168-8278(02)00042-9, PII S0168827802000429
-
Loréal O, Turlin B, Pigeon C, et al. Aceruloplasminemia: new clinical, pathophysiological and therapeutic insights. J Hepatol. 2002;36:851-856. (Pubitemid 35177417)
-
(2002)
Journal of Hepatology
, vol.36
, Issue.6
, pp. 851-856
-
-
Loreal, O.1
Turlin, B.2
Pigeon, C.3
Moisan, A.4
Ropert, M.5
Morice, P.6
Gandon, Y.7
Jouanolle, A.-M.8
Verin, M.9
Hider, R.C.10
Yoshida, K.11
Brissot, P.12
-
5
-
-
0037103195
-
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
-
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
-
7
-
-
2442671766
-
Serum ceruloplasmin and ferroxidase activity are not decreased in hepatic failure related to alcoholic cirrhosis: Clinical and pathophysiological implications
-
DOI 10.1097/01.ALC.0000125341.42253.C2
-
Le Lan C, Ropert M, Lainé F, et al. Serum ceruloplasmin and ferroxidase activity are not decreased in hepatic failure related to alcoholic cirrhosis: clinical and pathophysiological implications. Alcohol Clin Exp Res. 2004;28:775-779. (Pubitemid 38661375)
-
(2004)
Alcoholism: Clinical and Experimental Research
, vol.28
, Issue.5
, pp. 775-779
-
-
Lan, C.L.1
Ropert, M.2
Laine, F.3
Medevielle, M.4
Jard, C.5
Pouchard, M.6
Treut, A.L.7
Moirand, R.8
Loreal, O.9
Brissot, P.10
-
8
-
-
52449131277
-
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
-
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
-
-
0036800145
-
The copper-iron connection: Hereditary aceruloplasminemia
-
Nittis T, Gitlin JD. The copper-iron connection: hereditary aceruloplasminemia. Semin Hematol. 2002;39:282-289.
-
(2002)
Semin Hematol
, vol.39
, pp. 282-289
-
-
Nittis, T.1
Gitlin, J.D.2
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