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Updated: Mar 12, 2026

Use of Ultra-high Field MRI in Small Rodent Models of Polycystic Kidney Disease for In Vivo Phenotyping and Drug Monitoring
Published on: June 23, 2015
Current recommendations for treating autosomal dominant polycystic kidney disease
1Becky Ness practices nephrology at the Mayo Clinic Health System in Mankato, Minn. Kathryn Stovall practices at Durham (N.C.) Nephrology. The authors have disclosed no potential conflicts of interest, financial or otherwise.
Abstract:
Autosomal dominant polycystic kidney disease is the most common inherited kidney disease in the United States, causing hypertension, cerebral aneurysms, nephrolithiasis, and kidney failure. This article reviews the pathogenesis, diagnosis, associated complications, and current treatment recommendations for the condition.
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