Autosomal dominant polycystic kidney disease: Emerging concepts of pathogenesis and new treatments

被引：33
作者：
Braun, William E. [1 ]
机构：
[1] Cleveland Clin, Glickman Urol & Kidney Inst, Dept Hypertens & Nephrol, Transplantat Ctr, Cleveland, OH 44195 USA
来源：
CLEVELAND CLINIC JOURNAL OF MEDICINE | 2009年 / 76卷 / 02期
关键词：
RENAL-FAILURE; PROGRESSION; INHIBITION; VOLUME; CYSTOGENESIS; PATHWAY; CELLS; MTOR;
D O I：
10.3949/ccjm.76a.gr001
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Some of the mystery of autosomal dominant polycystic kidney disease (ADPKD) is starting to clear. Basic research is shedding light on its pathogenesis, and new treatments are in clinical trials. This paper reviews some of these advances and what they mean to patients.
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收藏
页码：97 / 104
页数：8
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