Ceruloplasmin deficiency

Known as: ACERULOPLASMINEMIA, Hypoceruloplasminemia 
 
National Institutes of Health

Papers overview

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Review
2008
Review
2008
Two decades ago, patients lacking circulating serum ceruloplasmin (Cp) presented with neurodegeneration associated with brain… (More)
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Highly Cited
2007
Highly Cited
2007
Ferroportin (Fpn), a ferrous iron Fe(II) transporter responsible for the entry of iron into plasma, is regulated post… (More)
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Highly Cited
2004
Highly Cited
2004
Significant increase in iron occurs in the substantia nigra pars compacta of Parkinsonian subjects, and in 6-hydroxydopamine (6… (More)
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Review
2002
Review
2002
Ceruloplasmin is a serum ferroxidase that contains greater than 95% of the copper found in plasma. This protein is a member of… (More)
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Highly Cited
2002
Highly Cited
2002
Ceruloplasmin is a ferroxidase that oxidizes toxic ferrous iron to its nontoxic ferric form. We have previously reported that a… (More)
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Highly Cited
1999
Highly Cited
1999
Aceruloplasminemia is an autosomal recessive disorder of iron metabolism. Affected individuals evidence iron accumulation in… (More)
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Highly Cited
1997
Highly Cited
1997
Ceruloplasmin is a copper-binding protein, which is the major ferroxidase in plasma of hepatic origin. We now provide evidence… (More)
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1996
1996
Hereditary ceruloplasmin deficiency with hemosiderosis (aceruloplasminemia) is a new disease characterized by systemic… (More)
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Highly Cited
1995
Highly Cited
1995
A hereditary ceruloplasmin deficiency associated with severe iron deposition in visceral organ and brain tissues found on… (More)
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Highly Cited
1995
Highly Cited
1995
We identified a mutation in the ceruloplasmin (Cp) gene in a Japanese family with aceruloplasminemia, some of whose members… (More)
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