Pediatric combined living donor liver and kidney transplantation for primary hyperoxaluria type 2
Author:
Publisher
Elsevier BV
Subject
Pharmacology (medical),Transplantation,Immunology and Allergy
Reference14 articles.
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2. Molecular analysis of the glyoxylate reductase (GRHPR) gene and description of mutations underlying primary hyperoxaluria type 2;Cregeen;Hum Mutat,2003
3. Primary and secondary hyperoxaluria: understanding the enigma;Bhasin;World J Nephrol,2015
4. Erythropoietin resistance as a result of oxalosis in bone marrow;Sahin;Clin Nephrol,2005
5. Hypothyroidism in primary hyperoxaluria type 1;Frishberg;J Pediatr,2000
Cited by 3 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. Primary hyperoxaluria: Long‐term outcomes of isolated kidney versus simultaneous liver/kidney transplant;Journal of Pediatric Gastroenterology and Nutrition;2024-07-15
2. Clinical features and mutational spectrum of Chinese patients with primary hyperoxaluria type 2;Urolithiasis;2024-05-10
3. Navigating the Evolving Landscape of Primary Hyperoxaluria: Traditional Management Defied by the Rise of Novel Molecular Drugs;Biomolecules;2024-04-23
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