Phenotypic Variability in Siblings With Autosomal Recessive Polycystic Kidney Disease
Author:
Funder
Bundesministerium für Bildung und Forschung Dienststelle Berlin
University of Cologne
Publisher
Elsevier BV
Subject
Nephrology
Reference28 articles.
1. Clinical courses and complications of young adults with autosomal recessive polycystic kidney disease (ARPKD);Burgmaier;Sci Rep,2019
2. Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphology;Zerres;Am J Med Genet,1998
3. Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1);Bergmann;J Am Soc Nephrol,2003
4. Autosomal recessive polycystic kidney disease: the clinical experience in North America;Guay-Woodford;Pediatrics,2003
5. Survival of childhood polycystic kidney disease following renal transplantation: the impact of advanced hepatobiliary disease;Davis;Pediatr Transplant,2003
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1. Epidemiology and outcomes of pediatric autosomal recessive polycystic kidney disease in the Middle East and North Africa;Pediatric Nephrology;2024-01-23
2. A decision‐making framework for genomic testing in paediatric nephrology;Journal of Paediatrics and Child Health;2023-11-17
3. Autosomal Recessive Polycystic Kidney Disease: Diagnosis, Prognosis, and Management;Advances in Kidney Disease and Health;2023-09
4. Portal hypertension syndrome in children with autosomal recessive polycystic kidney disease with liver cysts and hepatic fibrosis;Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics);2023-07-15
5. Polycystic Kidney Disease: ADPKD and ARPKD;Pediatric Kidney Disease;2023
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