Long-term outcome of transjugular intrahepatic portosystemic shunt for portal hypertension in autosomal recessive polycystic kidney disease
Author:
Publisher
Elsevier BV
Subject
Gastroenterology,Hepatology
Reference27 articles.
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2. Clinical and molecular characterization defines a broadened spectrum of autosomal recessive polycystic kidney disease (ARPKD);Adeva;Medicine,2006
3. Kidney versus combined kidney and liver transplantation in young people with autosomal recessive polycystic kidney disease: data from the European Society for Pediatric Nephrology/European Renal Association- European Dialysis and Transplant (ESPN/ERA-EDTA);Mekahli;Am J Kidney Dis,2016
4. Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes;Büscher;Pediatr Nephrol,2014
5. Liver disease in autosomal recessive polycystic kidney disease;Shneider;Pediatr Transplant,2005
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1. Case report: Rare genetic liver disease - a case of congenital hepatic fibrosis in adults with autosomal dominant polycystic kidney disease;Frontiers in Medicine;2024-02-07
2. Pre-emptive transjugular intrahepatic portosystemic shunt in pediatric cystic fibrosis-related liver disease and portal hypertension: prospective long-term results;Diagnostic and Interventional Radiology;2024-01-01
3. Autosomal Recessive Polycystic Kidney Disease: Diagnosis, Prognosis, and Management;Advances in Kidney Disease and Health;2023-09
4. Transjugular Intrahepatic Portosystemic Shunts in Pediatric Portal Hypertension: A Systematic Review and Meta-Analysis;Journal of Vascular and Interventional Radiology;2023-08
5. Transjugular intrahepatic portosystemic shunt for portal hypertension in a patient with Caroli disease;Asian Journal of Surgery;2023-07
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