New approaches to the autosomal recessive polycystic kidney disease patient with dual kidney-liver complications
Author:
Publisher
Wiley
Subject
Transplantation,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/petr.12076/fullpdf
Reference41 articles.
1. Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: Summary statement of a first National Institutes of Health/Office of Rare Diseases conference;Gunay-Aygun;J Pediatr,2006
2. Autosomal recessive polycystic kidney disease: Long-term outcome of neonatal survivors;Roy;Pediatr Nephrol,1997
3. Clinical and molecular characterisations defines a broadened spectrum of autosomal recessive polycystic disease (ARPKD);Adeva;Medicine,2006
4. Polycystic disease of kidney and liver presenting in childhood;Blyth;J Med Genet,1971
5. Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF);Turkbey;Pediatr Radiol,2009
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3. Autosomal Recessive Polycystic Kidney Disease: Diagnosis, Prognosis, and Management;Advances in Kidney Disease and Health;2023-09
4. Polycystic Kidney Disease: ADPKD and ARPKD;Pediatric Kidney Disease;2023
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