Investigations on the nature of ceruloplasmin deficiency in the newborn

Author:

Shokeir M. H. K.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference14 articles.

1. Studies on the rate of release and turnover of ceruloplasmin and apoceruloplasmin in rate plasma;Holtzman;J. Biol. Chem.,1970b

2. Physico-chemical properties of human ceruloplasmin;Kasper;J. Biol. Chem.,1963

3. Studies on the state of copper in native and modified human ceruloplasmin;Kasper;J Biol. Chem.,1963

4. Development of phenylalanine hydroxylase in mammalian liver;Kennedy;Science,1958

5. Physiologic” jaundice in newborn rhesus monkeys;Lucey;Amer. J. Dis. Child.,1963

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

2. Role of ceruloplasmin in nitric oxide metabolism in plasma of humans and sheep: a comparison of adults and fetuses;American Journal of Physiology-Regulatory, Integrative and Comparative Physiology;2013-12-01

3. Immunocytochemical identification of caeruloplasmin in hepatocytes of patients with Wilson's disease;Liver;2008-12-10

4. Diagnosis of Wilson's Disease: A Comprehensive Review;Critical Reviews in Clinical Laboratory Sciences;2008-01

5. Specific Oxidase Activity of Cord Serum Ceruloplasmin in the Newborn;Clinical Chemistry and Laboratory Medicine;2000-01-04

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