Prospective study on the potential of RAAS blockade to halt renal disease in Alport syndrome patients with heterozygous mutations. [electronic resource]
- Pediatric nephrology (Berlin, Germany) 01 2017
- 131-137 p. digital
Publication Type: Journal Article; Observational Study; Research Support, Non-U.S. Gov't
1432-198X
10.1007/s00467-016-3452-z doi
Adolescent Adult Age of Onset Child Child, Preschool Disease Progression Female Follow-Up Studies Genotype Heterozygote Humans Infant Infant, Newborn Kaplan-Meier Estimate Kidney Failure, Chronic--prevention & control Male Middle Aged Mutation Nephritis, Hereditary--complications Prospective Studies Renal Insufficiency, Chronic--drug therapy Renin-Angiotensin System--drug effects Treatment Outcome Young Adult