Combined liver-kidney transplantation for children with autosomal recessive polycystic kidney disease (ARPKD): indication and outcome-Reference-Cited by-同舟云学术

Combined liver-kidney transplantation for children with autosomal recessive polycystic kidney disease (ARPKD): indication and outcome

Published:2013-04-15 Issue:6 Volume:26 Page:640-650
ISSN:0934-0874
Container-title:Transplant International
language:en
Short-container-title:Transpl Int

Author:

Brinkert Florian¹,Lehnhardt Anja²,Montoya Carmen³,Helmke Knut⁴,Schaefer Hansjoerg⁵,Fischer Lutz⁶,Nashan Bjoern⁶,Bergmann Carsten,Ganschow Rainer⁷,Kemper Markus J.²

Affiliation:

1. Department of Pediatrics; Pediatric Gastroenterology and Hepatology; University Medical Center Hamburg-Eppendorf; Hamburg; Germany

2. Department of Pediatrics; Pediatric Nephrology; University Medical Center Hamburg-Eppendorf; Hamburg; Germany

3. Department of Pediatrics; Pediatric Nephrology; Children's Hospital Munich-Schwabing; Munich; Germany

4. Department of Pediatric Radiology; University Medical Center Hamburg-Eppendorf; Hamburg; Germany

5. Department of Pathology; University Medical Center Hamburg-Eppendorf; Hamburg; Germany

6. Department of Hepatobiliary Surgery and Visceral Transplantation; University Medical Center Hamburg-Eppendorf; Hamburg; Germany

7. Pediatric Hepatology and Liver Transplantation; University Medical Center Hamburg-Eppendorf; Hamburg; Germany

Publisher

Frontiers Media SA

Subject

Transplantation

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/tri.12098/fullpdf

Reference22 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. Educational paper: ciliopathies;Bergmann;Eur J Pediatr,2012

3. PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD);Bergmann;Hum Mutat,2004

4. The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein;Ward;Nat Genet,2002

5. Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD);Bergmann;Kidney Int,2005

Cited by 36 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Clinical Outcomes and Quality of Life of Patients Receiving Multi-Solid-Organ Transplants in Childhood Are Excellent: Results From a 20-Year Cohort Study;Transplant International;2024-08-14

2. Short-Term Outcome of Isolated Kidney Transplantation in Children with Autosomal Recessive Polycystic Kidney Disease: A Case Series and Literature Review;Clinics and Practice;2023-12-21

3. Autosomal Recessive Polycystic Kidney Disease: Diagnosis, Prognosis, and Management;Advances in Kidney Disease and Health;2023-09

4. Long-term outcome after combined or sequential liver and kidney transplantation in children with infantile and juvenile primary hyperoxaluria type 1;Frontiers in Pediatrics;2023-03-17

5. Growth and Puberty in Chronic Kidney Disease;Pediatric Kidney Disease;2023