Atypical and secondary hemolytic uremic syndromes have a distinct presentation and no common genetic risk factors. [electronic resource]
Producer: 20200921Description: 1443-1452 p. digitalISSN:- 1523-1755
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Antibodies, Monoclonal, Humanized -- therapeutic use
- Atypical Hemolytic Uremic Syndrome -- genetics
- Child
- Child, Preschool
- Complement Activation -- genetics
- Complement Inactivating Agents -- therapeutic use
- Complement System Proteins -- genetics
- Disease Progression
- Female
- France -- epidemiology
- Hemolytic-Uremic Syndrome -- etiology
- Humans
- Kidney -- immunology
- Kidney Failure, Chronic -- epidemiology
- Male
- Middle Aged
- Plasmapheresis -- statistics & numerical data
- Registries -- statistics & numerical data
- Renal Dialysis -- statistics & numerical data
- Renal Insufficiency, Chronic -- epidemiology
- Retrospective Studies
- Risk Factors
- Treatment Outcome
- Young Adult
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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