Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype. [electronic resource]
Producer: 20110121Description: 1844-59 p. digitalISSN:- 1555-905X
- Adolescent
- Adult
- Aged, 80 and over
- Autoantibodies -- blood
- Chi-Square Distribution
- Complement C3 -- genetics
- Complement Factor H -- genetics
- Complement System Proteins -- genetics
- DNA Mutational Analysis
- Disease-Free Survival
- Female
- Gene Frequency
- Genetic Predisposition to Disease
- Genetic Testing
- Hemolytic-Uremic Syndrome -- genetics
- Humans
- Infant
- Infant, Newborn
- Kaplan-Meier Estimate
- Kidney Transplantation
- Male
- Membrane Cofactor Protein -- genetics
- Mutation
- Pedigree
- Phenotype
- Polymorphism, Genetic
- Proportional Hazards Models
- Recurrence
- Registries
- Risk Assessment
- Risk Factors
- Thrombomodulin -- genetics
- Time Factors
- Treatment Outcome
- Young Adult
No physical items for this record
Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.