Reduced serum ceruloplasmin levels in hereditary haemochromatosis

British Journal of Haematology

Volumn 114, Issue 1, 2001, Pages 226-229

  Cairo, Gaetano ^a,b   Conte, Dario ^a   Bianchi, Laura ^a   Fraquelli, Mirella ^a   Recalcati, Stefania ^a  

^a UNIVERSITY OF MILAN   (Italy)

^b CNR   (Italy)

Author keywords

Ceruloplasmin; Copper; Ferroxidase; Haemochromatosis; Iron

Indexed keywords

CERULOPLASMIN; COPPER; GENE PRODUCT; HFE PROTEIN; IRON; OROSOMUCOID; UNCLASSIFIED DRUG;

ADULT; ARTICLE; CERULOPLASMIN BLOOD LEVEL; CLINICAL ARTICLE; CONTROLLED STUDY; GENE MUTATION; HEMOCHROMATOSIS; HUMAN; IRON KINETICS; IRON OVERLOAD; PHLEBOTOMY; PRIORITY JOURNAL;

ADULT; CASE-CONTROL STUDIES; CERULOPLASMIN; FEMALE; HEMOCHROMATOSIS; HUMANS; IRON OVERLOAD; MALE; MIDDLE AGED; PHLEBOTOMY; STATISTICS, NONPARAMETRIC;

EID: 0034934762     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2001.02917.x     Document Type: Article

References (12)

1. EASL International Consensus Conference on Hemochromatosis
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5. The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22
6. Screening for Wilson's disease in patients with liver diseases by serum ceruloplasmin
7. Liver pathology in genetic hemochromatosis: A review of 135 homozygous cases and their bioclinical correlations
8. Transcriptional regulation of ceruloplasmin gene expression during inflammation
9. Mechanisms of caeruloplasmin biosynthesis in normal and copper-deficient rats
10. Regulation of hepatic transferrin, transferrin receptor and ferritin genes in human siderosis
11. Hereditary hemochromatosis in adults without pathogenic mutations in the hemochromatosis gene
12. Heterogeneity of hemochromatosis in Italy