Autosomal Recessive Polycystic Kidney Disease
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Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-52719-8_117
Reference94 articles.
1. Bergmann C, et al. Polycystic kidney disease. Nat Rev Dis Primers. 2018;4(1):50.
2. Guay-Woodford LM. Autosomal recessive polycystic kidney disease: the prototype of the hepato-renal fibrocystic diseases. J Pediatr Genet. 2014;3(2):89–101.
3. Habbig S, Liebau MC. Ciliopathies – from rare inherited cystic kidney diseases to basic cellular function. Mol Cell Pediatr. 2015;2(1):8.
4. Guay-Woodford LM, et al. Consensus expert recommendations for the diagnosis and management of autosomal recessive polycystic kidney disease: report of an international conference. J Pediatr. 2014;165(3):611–7.
5. Gimpel C, et al. Perinatal diagnosis, management, and follow-up of cystic renal diseases: a clinical practice recommendation with systematic literature reviews. JAMA Pediatr. 2018;172(1):74–86.
Cited by 2 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. 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
2. Ameliorating liver disease in an autosomal recessive polycystic kidney disease mouse model;American Journal of Physiology-Gastrointestinal and Liver Physiology;2023-05-01
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