(Q44014364)

28 November 2017

Aceruloplasminemia: new clinical, pathophysiological and therapeutic insights (English)

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28 November 2017

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Olivier Loréal

1

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28 November 2017

Bruno Turlin

2

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28 November 2017

Christelle Pigeon

3

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28 November 2017

Annick Moisan

4

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28 November 2017

Martine Ropert

5

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28 November 2017

Patrick Morice

6

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28 November 2017

Yves Gandon

7

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28 November 2017

Anne-Marie Jouanolle

8

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28 November 2017

Marc Vérin

9

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28 November 2017

Robert C Hider

10

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28 November 2017

Kunihiro Yoshida

11

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28 November 2017

Pierre Brissot

12

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28 November 2017

1 June 2002

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28 November 2017

Journal of Hepatology

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28 November 2017

36

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28 November 2017

6

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28 November 2017

851-856

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Haemochromatosis: novel gene discovery and the molecular pathophysiology of iron metabolism

28 November 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Aceruloplasminemia: molecular characterization of this disorder of iron metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Role of ceruloplasmin in cellular iron uptake

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Iron metabolism in eukaryotes: Mars and Venus at it again

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Quantification of non-transferrin-bound iron in the presence of unsaturated transferrin

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Hemochromatosis: diagnosis and quantification of liver iron with gradient-echo MR imaging

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Complete cDNA sequence of human preceruloplasmin

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Ascorbic acid status in idiopathic hemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

A nonsense mutation of the ceruloplasmin gene in hereditary ceruloplasmin deficiency with diabetes mellitus

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Estimation of the gene frequency of aceruloplasminemia in Japan

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Expression of the ceruloplasmin gene in the human retina and brain: implications for a pathogenic model in aceruloplasminemia

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

A novel glycosylphosphatidylinositol-anchored form of ceruloplasmin is expressed by mammalian astrocytes.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Alternative RNA splicing generates a glycosylphosphatidylinositol-anchored form of ceruloplasmin in mammalian brain

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Intestinal absorption and enterohepatic cycling of biliary iron originating from plasma non-transferrin-bound iron in rats

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Genes that modify the hemochromatosis phenotype in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Increased very long-chain fatty acids in erythrocyte membranes of patients with aceruloplasminemia

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Increased plasma lipid peroxidation in patients with aceruloplasminemia

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Liver pathology in genetic hemochromatosis: a review of 135 homozygous cases and their bioclinical correlations

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

A new syndrome of liver iron overload with normal transferrin saturation.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Histologic features of the liver in insulin resistance-associated iron overload. A study of 139 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Long-term survival in patients with hereditary hemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Obesity, body fat distribution, insulin sensitivity and Islet beta-cell function as explanations for metabolic diversity

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Use of desferrioxamine in the treatment of aceruloplasminemia

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

Investigation into the correlation between the structure of hydroxypyridinones and blood-brain barrier permeability.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900042-9

7 January 2021

10.1016/S0168-8278(02)00042-9

Identifiers

DOI

1 reference

28 November 2017

1 reference