Autosomal-Recessive Polycystic Kidney Disease Gets More Complex
Author:
Publisher
Elsevier BV
Subject
Gastroenterology,Hepatology
Reference8 articles.
1. Characteristics of Congenital Hepatic Fibrosis in a Large Cohort of Patients With Autosomal Recessive Polycystic Kidney Disease
2. PKHD1 sequence variations in 78 children and adults with autosomal recessive polycystic kidney disease and congenital hepatic fibrosis
3. Correlation of Kidney Function, Volume and Imaging Findings, andPKHD1Mutations in 73 Patients with Autosomal Recessive Polycystic Kidney Disease
4. Autosomal Recessive Polycystic Kidney Disease: The Clinical Experience in North America
5. Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD)
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1. Polycystic Kidney Diseases and Other Hepatorenal Fibrocystic Diseases;Kidney Development, Disease, Repair and Regeneration;2016
2. Childhood Polycystic Kidney Disease;Pediatric Nephrology;2015-11-12
3. Autosomal recessive polycystic kidney disease: The prototype of the hepato-renal fibrocystic diseases;Journal of Pediatric Genetics;2015-07-27
4. Polycystic Kidney Disease;Chronic Renal Disease;2015
5. Childhood Polycystic Kidney Disease;Pediatric Nephrology;2015
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