Hereditary hypoceruloplasminemia

Author:

Edwards C. Q.,Williams D. M.,Cartwright G. E.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference18 articles.

1. The pathogenesis and evolution of Wilson's disease;Cartwright;Epatologia,1974

2. Studies on copper metabolism. XXIX. A critical analysis of serum copper and ceruloplasmin concentrations in normal subjects, patients with Wilson's disease and relatives of patients with Wilson's disease;Cartwright;Amer. J. Med.,1960

3. Copper metabolism in normal subjects;Cartwright;Amer. J. din. Nut.,1964

4. Factors influencing ceruloplasmin levels in normal individuals;Cox;J. Lab. din. Med.,1966

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1. Inherited Disorders of Iron Overload;Frontiers in Nutrition;2018-10-29

2. Wilson Disease;Clinics in Liver Disease;2017-11

3. A century for progress in the diagnosis of Wilson disease;Journal of Trace Elements in Medicine and Biology;2014-10

4. Uneven distribution of hepatic copper concentration and diagnostic value of double-sample biopsy in Wilson's disease;Scandinavian Journal of Gastroenterology;2013-10-28

5. Re-evaluation of the diagnostic criteria for Wilson disease in children with mild liver disease;Hepatology;2010-10-21

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