Keine generelle Empfehlung zur Nephrektomie bei pränatalem Verdacht auf ARPKD
Author:
Publisher
Springer Science and Business Media LLC
Subject
Urology
Link
http://link.springer.com/content/pdf/10.1007/s00120-017-0500-7.pdf
Reference12 articles.
1. Ebner K, Liebau MC (2014) Autosomal-rezessive polyzystische Nierenerkrankung: Klinik, therapeutische Optionen und neue Entwicklungen. Nephrol 9(4):312–318
2. Lu H, Galeano MCR, Ott E, Kaeslin G, Kausalya PJ, Kramer C et al (2017) Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease. Nat Genet 49(7):1025. https://doi.org/10.1038/ng.3871
3. Guay-Woodford LM, Bissler JJ, Braun MC, Bockenhauer D, Cadnapaphornchai MA, Dell KM et al (2014) Consensus expert recommendations for the diagnosis and management of autosomal recessive polycystic kidney disease: report of an international conference. J Pediatr 165(3):611–617
4. Guay-Woodford LM, Desmond RA (2003) Autosomal recessive polycystic kidney disease: the clinical experience in North America. Pediatrics 111(5 Pt 1):1072–1080
5. Bergmann C, Senderek J, Windelen E, Küpper F, Middeldorf I, Schneider F et al (2005) Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD). Kidney Int 67(3):829–848
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