Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease—different clinical entities and comparable perinatal renal abnormalities-Reference-Cited by-同舟云学术

Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease—different clinical entities and comparable perinatal renal abnormalities

Published:2017-01-12 Issue:5 Volume:32 Page:791-800
ISSN:0931-041X
Container-title:Pediatric Nephrology
language:en
Short-container-title:Pediatr Nephrol

Author:

Hackl Agnes,Mehler Katrin,Gottschalk Ingo,Vierzig Anne,Eydam Marcus,Hauke Jan,Beck Bodo B.,Liebau Max C.,Ensenauer Regina,Weber Lutz T.,Habbig Sandra

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00467-016-3556-5.pdf

Reference45 articles.

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2. Bergmann C (2015) ARPKD and early manifestations of ADPKD: the original polycystic kidney disease and phenocopies. Pediatr Nephrol 30:15–30

3. Cramer MT, Guay-Woodford LM (2015) Cystic kidney disease: a primer. Adv Chronic Kidney Dis 22:297–305

4. Hildebrandt F, Benzing T, Katsanis N (2011) Ciliopathies. N Engl J Med 364:1533–1543

5. Habbig S, Liebau MC (2015) Ciliopathies—from rare inherited cystic kidney diseases to basic cellular function. Mol Cell Pediatr 2:8

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