Individualized concept for the treatment of autosomal recessive polycystic kidney disease with end‐stage renal disease-Reference-Cited by-同舟云学术

Individualized concept for the treatment of autosomal recessive polycystic kidney disease with end‐stage renal disease

Published:2020-03-03 Issue:3 Volume:24 Page:
ISSN:1397-3142
Container-title:Pediatric Transplantation
language:en
Short-container-title:Pediatr Transplant

Author:

Miura Kenichiro¹^ORCID,Sato Yasuyuki²,Yabuuchi Tomoo¹,Kaneko Naoto¹,Ishizuka Kiyonobu¹,Chikamoto Hiroko¹,Akioka Yuko¹³,Nawashiro Yuri⁴,Hisano Masataka⁴,Imamura Hideaki⁵,Miyai Takayuki⁶,Sakamoto Seisuke⁷^ORCID,Kasahara Mureo⁷^ORCID,Fuchinoue Shohei⁸,Okumi Masayoshi⁹,Ishida Hideki⁹,Tanabe Kazunari⁹,Hattori Motoshi¹^ORCID

Affiliation:

1. Department of Pediatric Nephrology Tokyo Women's Medical University Tokyo Japan

2. Department of Pediatrics Hokkaido University Graduate School of Medicine Sapporo Japan

3. Department of Pediatrics Saitama Medical University Saitama Japan

4. Department of Nephrology Chiba Children's Hospital Chiba Japan

5. Division of Pediatrics Department of Reproductive and Developmental Medicine Faculty of Medicine University of Miyazaki Miyazaki Japan

6. Department of Pediatrics Okayama University Hospital Okayama Japan

7. Organ Transplantation Center National Center for Child Health and Development Tokyo Japan

8. Department of Surgery Kidney Center Tokyo Women's Medical University Tokyo Japan

9. Department of Urology Tokyo Women's Medical University Tokyo Japan

Funder

Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan

Publisher

Wiley

Subject

Transplantation,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/petr.13690

Reference34 articles.

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

2. Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD)

3. Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes

4. Consensus Expert Recommendations for the Diagnosis and Management of Autosomal Recessive Polycystic Kidney Disease: Report of an International Conference

5. Autosomal-recessive polycystic kidney disease

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