Noris, Marina <br/><br/>
Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype.  [electronic resource] 

 -  Clinical journal of the American Society of Nephrology : CJASN  Oct 2010 
 - 1844-59 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1555-905X 
<br/><br/><label>Standard No.: </label>10.2215/CJN.02210310  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged, 80 and over<br/>Autoantibodies--blood<br/>Chi-Square Distribution<br/>Complement C3--genetics<br/>Complement Factor H--genetics<br/>Complement System Proteins--genetics<br/>DNA Mutational Analysis<br/>Disease-Free Survival<br/>Female<br/>Gene Frequency<br/>Genetic Predisposition to Disease<br/>Genetic Testing<br/>Hemolytic-Uremic Syndrome--genetics<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Kaplan-Meier Estimate<br/>Kidney Transplantation<br/>Male<br/>Membrane Cofactor Protein--genetics<br/>Mutation<br/>Pedigree<br/>Phenotype<br/>Polymorphism, Genetic<br/>Proportional Hazards Models<br/>Recurrence<br/>Registries<br/>Risk Assessment<br/>Risk Factors<br/>Thrombomodulin--genetics<br/>Time Factors<br/>Treatment Outcome<br/>Young Adult