Clinical features of cyst infection and hemorrhage in ADPKD: new diagnostic criteria

Author:

Suwabe Tatsuya,Ubara Yoshifumi,Sumida Keiichi,Hayami Noriko,Hiramatsu Rikako,Yamanouchi Masayuki,Hasegawa Eiko,Hoshino Junichi,Sawa Naoki,Saitoh Satoshi,Okuda Itsuko,Takaichi Kenmei

Publisher

Springer Science and Business Media LLC

Subject

Physiology (medical),Nephrology,Physiology

Reference24 articles.

1. Torres VE. Polycystic kidney disease autosomal-dominant and recessive forms. In: Massry SG, Glassock RJ (eds) Textbook of nephrology, 4th edn. Philadelphia: Lippincott Williams & Wilkins; 2001. p. 896–904.

2. Fick GM, Johnson AM, Hammomd WS, Gabow PA. Causes of death in autosomal dominant polycystic kidney disease. J Am Soc Nephrol. 1995;5:2048–56.

3. Peter CH, Vicente ET. Autosomal dominant polycystic kidney disease. Gene reviews. Bethesda: National Institutes of Health; 2009.

4. Suwabe T, Ubara Y, Higa Y, Nakanishi S, Sogawa Y, Nomura K, et al. Infected hepatic and renal cysts: differential impact on outcome in autosomal dominant polycystic kidney disease. Nephron Clin Prac. 2009;112:c157–63.

5. Elzinga LW, Bennett WM. Miscellaneous renal and systemic complications of autosomal dominant polycystic kidney disease including infection. In: Watson ML, Torres VE, editors. Polycystic kidney disease. Northants: Oxford Medical; 1996. p. 483–99.

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