Comparison of phenotypes of polycystic kidney disease types 1 and 2

1999/01/01 by Nick Hateboer, Marjan A. van Dijk, Marjan A v Dijk +12 · 8 citations
Biochemistry, Genetics and Molecular Biology · Medicine · #Genetic and Kidney Cyst Diseases #Pediatric Urology and Nephrology Studies #Vascular Malformations and Hemangiomas

paper · doi:10.1016/s0140-6736(98)03495-3

crossref issued 1999/01/01 · crossref published 1999/01/01 · crossref published-print 1999/01/01 · openalex publication_date 1999/01/01 · crossref created 2002/07/26 · openalex created_date 2016/06/24 · crossref deposited 2021/05/13 · crossref indexed 2026/05/20 · openalex updated_date 2026/07/22

Cited by

• Autosomal dominant polycystic kidney disease
• Estimating prevalence in single-gene kidney diseases progressing to renal failure
• A Loss-of-Function Model for Cystogenesis in Human Autosomal Dominant Polycystic Kidney Disease Type 2
• Progressive Loss of Renal Function Is an Age-Dependent Heritable Trait in Type 1 Autosomal Dominant Polycystic Kidney Disease
• Imaging Classification of Autosomal Dominant Polycystic Kidney Disease
• Autosomal Dominant Polycystic Kidney Disease
• Comparison between siblings and twins supports a role for modifier genes in ADPKD
• Autosomal dominant polycystic kidney disease [wikipedia]