Literature DB >> 14279137

DIAGNOSTIC VALUE OF SERUM COMPLEMENT DETERMINATION IN HEREDITARY GLOMERULONEPHRITIS.

E WASSERMAN, F SCHWARZ, M WACHSTEIN, K LANGE.   

Abstract

Keywords:  COMPLEMENT; DIAGNOSIS, DIFFERENTIAL; GENETICS, HUMAN; GLOMERULONEPHRITIS; HEMATURIA

Mesh：

Substances：

Year:  1965        PMID： 14279137

Source DB:  PubMed          Journal:  J Lab Clin Med        ISSN： 0022-2143


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  5 in total

1.  Segregation ratios in Alport's syndrome.

Authors:  E MacNeill; R F Shaw
Journal:  J Med Genet       Date:  1973-03       Impact factor: 6.318

2.  Correspondence: Alport's syndrome.

Authors:  O Mayo
Journal:  J Med Genet       Date:  1973-12       Impact factor: 6.318

3.  Recurrent haematuria in childhood. A five-year follow-up.

Authors:  C Johnston; S Shuler
Journal:  Arch Dis Child       Date:  1969-08       Impact factor: 3.791

4.  Serum C3 levels in acute glomerulonephritis and postnephritic children.

Authors:  M Popovic-Rolovic
Journal:  Arch Dis Child       Date:  1973-08       Impact factor: 3.791

5.  Estimation of beta-IG globulin in glomerulonephritis.

Authors:  S W Epstein; S Dubiski; J D Fitzgerald
Journal:  Can Med Assoc J       Date:  1967-04-29       Impact factor: 8.262
  5 in total

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