No common final pathogenetic pathway in haemolytic uraemic syndromes

Nephrology Dialysis Transplantation

Volumn 14, Issue 5, 1999, Pages 1100-1102

  Taylor, C Mark ^a,b   Howie, Alexander J ^a   Williams, Julie M ^a  

^a UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^b BIRMINGHAM CHILDREN S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

HEMOLYTIC UREMIC SYNDROME; HUMAN; NOTE; PATHOGENESIS; PRIORITY JOURNAL;

EID: 0032892858     PISSN: 09310509     EISSN: None     Source Type: Journal    
DOI: 10.1093/ndt/14.5.1100     Document Type: Note

References (13)

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3. Habib R. Pathology of the hemolytic uremic syndrome. In: Kaplan BS, Trompeter RS Moake JL, eds. Hemolytic Uremic Syndrome and Thrombotic Thrombocytopenic Purpura. Marcel Dekker, New York: 1992: 315-353
4. Thoenes W, John HD. Endotheliotropic (haemolytic) nephroangiopathy and its various manifestations: thrombotic microangiopathy, primary malignant nephro-sclerosis, haemolytic uraemic syndrome. Klin Wochenschr 1980; 58: 173-184
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9. Ohali M, Shalev H, Schlesinger M et al. Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor H. Pediatr Nephrol 1998; 12: 619-624
10. Warwicker P, Donne RL, Goodship JA et al. Familial relapsing haemolytic uraemic syndrome and complement factor H deficiency. Nephrol Dial Transplant, submitted
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12. Heptinstall RM. Pathology of the Kidney 4th edn. Little Brown, Boston: 1992: 1172-1199
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