Recurrent haemolytic uraemic syndrome and acquired hypomorphic variant of the third component of complement-Reference-Cited by-同舟云学术

Recurrent haemolytic uraemic syndrome and acquired hypomorphic variant of the third component of complement

Published:1990-11 Issue:6 Volume:4 Page:597-599
ISSN:0931-041X
Container-title:Pediatric Nephrology
language:en
Short-container-title:Pediatr Nephrol

Author:

Roodhooft A. M.,McLean R. H.,Elst E.,Van Acker K. J.

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/BF00858631.pdf

Reference12 articles.

1. Habib R, Levy M, Gagnadoux M-F, Broyer M (1981) Le pronostic du syndrome hémolytique et urémique chez l'enfant. In: Actualités Néphrologiques de l'Hôpital Necker. Habib R, Broyer M (eds) Flammarion Paris, p 245

2. Carreras L, Romero R, Requesens C, Oliver AJ, Carrera M, Clavo M, Alsina J (1981) Familial hypocomplementemic hemolytic uremic syndrome with HLA-A3, B7 haplotype. JAMA 245: 602?604

3. Thompson RA, Winterborn MH (1981) Hypocomplementaemia due to a genetic deficiency of BH globulin. Clin Exp Immunol 46: 110?119

4. Wyatt RJ, Jones D, Stapleton FB, Roy S III, Odom TW, McLean RH (1985) Recurrent hemolytic-uremic syndrome with the hypomorphic fast allele of the third component of complement. J Pediatr 107: 564?565

5. Laurell CB (1965) Electroimmunoassay. Anal Biochem 10: 358?361

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