H deficiency in two brothers with atypical dense intramembranous deposit disease

Author:

Levy Micheline,Halbwachs–Mecarelli Lise,Gubler Marie–Claire,Kohout Gérard,Bensenouci Abdelatif,Niaudet Patrick,Hauptmann Georges,Lesavre Philippe

Publisher

Elsevier BV

Subject

Nephrology

Reference39 articles.

1. Control of the amplification convertase of complement by the plasma protein β1H;Weiler;Proc Natl Acad Sci USA,1976

2. Human complement C3b inactivator: Isolation, characterization and demonstration of an absolute requirement for serum protein β1H for cleavage of C3b and C4b in solution;Pangburn;J Exp Med,1977

3. Requirements to β1H globulin and C3b inactivator in the control of the alternative complement pathway in human serum;Whaley;Immunology,1978

4. Complement deficiency states and infection: Epidemiology, pathogenesis and consequences of Neisserial and other infections in an immune deficiency;Ross;Medicine,1984

5. Hypocomplementaemia due to a genetic deficiency of β1H globulin;Thompson;Clin Exp Immunol,1981

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