Measurement of blood holoceruloplasmin by EIA using a mouse monoclonal antibody directed to holoceruloplasmin. Implication for mass screening of Wilson disease

Author:

Endo F.,Taketa K.,Nakamura K.,Awata H.,Tanoue A.,Eda Y.,Matsuda I.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference12 articles.

1. Bull PC, Thomas GR, Rommens JM et al (1993) The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene.Nature Genet 5: 327?337.

2. Danks DM (1989) Disorder of copper transport. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds.The Metabolic Basis of Inherited Disease, 6th edn. New York: McGraw Hill, 1411?1431.

3. Endo F, Tanoue A, Kitano A et al (1990) Biochemical basis of prolidase deficiency. Clinical phenotypes and RNA phenotypes and the relation to clinical phenotype.J Clin Invest 85: 162?169.

4. Holtzman NA, Naughton MA, Iber FL, Gaumnitz BM (1967) Ceruloplasmin in Wilson's disease.J Clin Invest 46: 993?1002.

5. Matsuda I, Pearson T, Holtzman NA (1974) Determination of apoceruloplasmin by radioimmunoassay in nutritional copper deficiency, Menkes' kinky hair syndrome, Wilson's disease, and umbilical cord blood.Pediatrics 8: 821?824.

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1. Population Screening for Wilson Disease;Clinical and Translational Perspectives on WILSON DISEASE;2019

2. Biochemical Diagnosis of Wilson Disease;Clinical and Translational Perspectives on WILSON DISEASE;2019

3. Quantification of ATP7B Protein in Dried Blood Spots by Peptide Immuno-SRM as a Potential Screen for Wilson’s Disease;Journal of Proteome Research;2016-12-09

4. Plasma exchange and chelator therapy rescues acute liver failure in Wilson disease without liver transplantation;Hepatology Research;2016-05-28

5. Diagnostic Value of Ceruloplasmin in the Diagnosis of Pediatric Wilson's Disease;Pediatric Gastroenterology, Hepatology & Nutrition;2015

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