Literature DB >> 13792199

A rapid screening test for deficiency of plasma ceruloplasmin and its value in the diagnosis of Wilson's disease.

P AISEN, J B SCHORR, A G MORELL, R Z GOLD, I H SCHEINBERG.   

Abstract

Entities:  

Keywords:  HEPATOLENTICULAR DEGENERATION/blood; SERUM GLOBULIN

Mesh：

Substances：

Year:  1960        PMID： 13792199     DOI： 10.1016/0002-9343(60)90149-2

Source DB:  PubMed          Journal:  Am J Med        ISSN： 0002-9343            Impact factor:   4.965


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  4 in total

1.  DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.

Authors:  I Sternlier; A G Morell; C D Bauer; B Combes; S De Bobes-Sternberg; I H Schein-Berg
Journal:  J Clin Invest       Date:  1961-04       Impact factor: 14.808

2.  Set of simple side-room urine tests for detection of inborn errors of metabolism.

Authors:  N R Buist
Journal:  Br Med J       Date:  1968-06-22

3.  A screening test for Wilson's disease and its application to psychiatric patients.

Authors:  D W Cox
Journal:  Can Med Assoc J       Date:  1967-01-14       Impact factor: 8.262

Review 4.  The screening of hereditary metabolic defects among newborn infants.

Authors:  D Y Hsia
Journal:  Can Med Assoc J       Date:  1966-08-06       Impact factor: 8.262
  4 in total

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