Familial Hemolytic-Uremic Syndrome and Homozygous Factor H Deficiency-Reference-Cited by-同舟云学术

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Familial Hemolytic-Uremic Syndrome and Homozygous Factor H Deficiency

Published:1994-12 Issue:6 Volume:24 Page:936-941
ISSN:0272-6386
Container-title:American Journal of Kidney Diseases
language:en
Short-container-title:American Journal of Kidney Diseases

Author:

Pichette Vincent,Quérin Serge,Schürch Walter,Brun Gaétane,Lehner-Netsch Gertrude,Delâge Jean-Marie

Publisher

Elsevier BV

Subject

Nephrology

Reference25 articles.

1. Vascular diseases of the kidney. Thrombotic microangiopathy (hemolytic-uremic syndrome and thrombotic thrombocytopenic purpura);Ives,1991

2. Hemolytic uremic syndrome in families;Kaplan;N Engl J Med,1975

3. Hemolytic-uremic syndrome;Kaplan,1990

4. Inherited hemolytic uremic syndrome in adults;Berns;Am J Kidney Dis,1992

5. Serum complement levels in haemolytic-uraemic syndrome;Kaplan;Lancet,1973

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1. Atypical Hemolytic Uremic Syndrome;Pediatric Kidney Disease;2023

2. Protein therapeutics and their lessons: Expect the unexpected when inhibiting the multi‐protein cascade of the complement system;Immunological Reviews;2022-11-18

3. The role of von Willebrand factor in thrombotic microangiopathy;Pediatric Nephrology;2017-07-26

4. Familial hemolytic uremic syndrome with occurrence in the postpartum period;Saudi Journal of Kidney Diseases and Transplantation;2017

5. Post-infectious Proliferative Glomerulonephritis with Monoclonal Immunoglobulin G Deposits Associated with Complement Factor H Mutation;Internal Medicine;2017

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