Autosomal dominant polycystic kidney disease: 2009 Update for internists

21Citations
Citations of this article
30Readers
Mendeley users who have this article in their library.

Abstract

Because autosomal dominant polycystic kidney disease (ADPKD) is one of the most common genetic abnormalities seen in today's medical practice, many internists will likely treat patients affected by this condition. Genetic abnormalities have been increasingly recognized, and the pathophysiology of the disease is beginning to be unraveled. Because of advances in imaging technology, surrogate markers for disease progression have allowed clinical studies of newer therapeutic agents to proceed. In the near future, therapies for this common genetic disease may be available to either prevent or stabilize the disease course for many affected individuals.

Cite

CITATION STYLE

APA

Bennett, W. M. (2009). Autosomal dominant polycystic kidney disease: 2009 Update for internists. Korean Journal of Internal Medicine. https://doi.org/10.3904/kjim.2009.24.3.165

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free