Autosomal-rezessive polyzystische Nierenerkrankung (ARPKD)
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
https://link.springer.com/content/pdf/10.1007/s11560-021-00559-2.pdf
Reference18 articles.
1. Guay-Woodford LM, Desmond RA (2003) Autosomal recessive polycystic kidney disease: the clinical experience in North America. Pediatrics 111:1072–1080
2. Büscher R, Büscher AK, Weber S et al (2014) Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes. Pediatr Nephrol 29:1915–1925. https://doi.org/10.1007/s00467-013-2634-1
3. Sweeney WE, Avner ED (2011) Diagnosis and management of childhood polycystic kidney disease. Pediatr Nephrol 26:675–692. https://doi.org/10.1007/s00467-010-1656-1
4. Gunay-Aygun M, Avner ED, Bacallao RL et al (2006) Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: summary statement of a first national institutes of health/office of rare diseases conference. J Pediatr 149:159–164. https://doi.org/10.1016/j.jpeds.2006.03.014
5. Ebner K, Liebau MC (2014) Autosomal-rezessive polyzystische Nierenerkrankung: Klinik, therapeutische Optionen und neue Entwicklungen. Nephrologie 9:312–318. https://doi.org/10.1007/s11560-014-0887-8
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