Familial haemolytic uraemic syndrome and an MCP mutation
- 1 November 2003
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 362 (9395) , 1542-1547
- https://doi.org/10.1016/s0140-6736(03)14742-3
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Renal transplantation in patients with hemolytic uremic syndrome: high rate of recurrence and increased incidence of acute rejections1Transplantation, 2003
- Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countriesJournal of Medical Genetics, 2003
- Shiga toxin-associated hemolytic uremic syndrome: absence of recurrence after renal transplantationPediatric Nephrology, 2002
- von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndromeBlood, 2002
- Factor H Mutations in Hemolytic Uremic Syndrome Cluster in Exons 18–20, a Domain Important for Host Cell RecognitionAmerican Journal of Human Genetics, 2001
- Clustering of Missense Mutations in the C-Terminal Region of Factor H in Atypical Hemolytic Uremic SyndromeAmerican Journal of Human Genetics, 2001
- Heterogeneity of atypical haemolytic uraemic syndromesArchives of Disease in Childhood, 1997
- Typical and Atypical Hemolytic Uremic SyndromeKidney and Blood Pressure Research, 1996
- Identification and characterization of membrane cofactor protein (CD46) in the human kidneysEuropean Journal of Immunology, 1994
- HEMOLYTIC-UREMIC SYNDROME IN ADULT SISTERSTransplantation, 1974