Fatal outcome of autosomal recessive polycystic kidney disease in neonates with recessive PKHD1 mutations-Reference-Cited by-同舟云学术

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Fatal outcome of autosomal recessive polycystic kidney disease in neonates with recessive PKHD1 mutations

Published:2020-05 Issue:19 Volume:99 Page:e20113
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:Medicine

Author:

Jung Jiwon,Seo Go Hun,Kim Yoo-Mi,Han Young Mi,Park Ji Kwon,Kim Gu-Hwan,Lee Joo Hoon,Park Young Seo,Lee Byong Sop,Kim Ellen Ai-Rhan,Lee Pil-Ryang,Lee Beom Hee

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference23 articles.

1. Autosomal recessive polycystic kidney disease

2. Clinical and Molecular Characterization Defines a Broadened Spectrum of Autosomal Recessive Polycystic Kidney Disease (ARPKD)

3. PKHD1 sequence variations in 78 children and adults with autosomal recessive polycystic kidney disease and congenital hepatic fibrosis

4. Autosomal Recessive Polycystic Kidney Disease: The Clinical Experience in North America

5. Prenatal ultrasound, genotype, and outcome in a large cohort of prenatally affected patients with autosomal-recessive polycystic kidney disease and other hereditary cystic kidney diseases

Cited by 1 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. How should we assess renal function in neonates and infants?;Acta Paediatrica;2020-09-18

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