Unilateral nephrectomy for young infants with congenital nephrotic syndrome of the Finnish type-Reference-Cited by-同舟云学术

Unilateral nephrectomy for young infants with congenital nephrotic syndrome of the Finnish type

Published:2021-09-28 Issue:2 Volume:26 Page:162-169
ISSN:1342-1751
Container-title:Clinical and Experimental Nephrology
language:en
Short-container-title:Clin Exp Nephrol

Author:

Murakoshi Miki,Kamei Koichi^ORCID,Ogura Masao,Sato Mai,Nada Taishi,Suzuki Ryutaro,Kamae Chikako,Nishi Kentaro,Kanamori Toru,Nagano China,Nozu Kandai,Nakanishi Koichi,Iijima Kazumoto

Publisher

Springer Science and Business Media LLC

Subject

Physiology (medical),Nephrology,Physiology

Link

https://link.springer.com/content/pdf/10.1007/s10157-021-02141-5.pdf

Reference27 articles.

1. Holmberg C, Antikainen M, Rönnholm K, Ala Houhala M, Jalanko H. Management of congenital nephrotic syndrome of the Finnish type. Pediatr Nephrol. 1995;9:87–93.

2. Holmberg C, Laine J, Rönnholm K, Ala-Houhala M, Jalanko H. Congenital nephrotic syndrome. Kidney Int Suppl. 1996;53:S51–6.

3. Patrakka J, Kestilä M, Wartiovaara J, Ruotsalainen V, Tissari P, Lenkkeri U, Männikkö M, Visapää I, Holmberg C, Rapola J, Tryggvason K, Jalanko H. Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients. Kidney Int. 2000;58:972–80.

4. Beltcheva O, Martin P, Lenkkeri U, Tryggvason K. Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome. Hum Mutat. 2001;17:368–73.

5. Sharief SN, Hefni NA, Alzahrani WA, Nazer II, Bayazeed MA, Alhasan KA, Safdar OY, El-Desoky SM, Kari JA. Genetics of congenital and infantile nephrotic syndrome. World J Pediatr. 2019;15:198–203.

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1. A Case of Congenital Nephrotic Syndrome with Crescents Caused by a Novel Compound Heterozygous Pairing of NPHS1 Genetic Variants;Case Reports in Nephrology;2024-02-27

2. Clinical presentation and management of nephrotic syndrome in the first year of life: A report from the Pediatric Nephrology Research Consortium;Frontiers in Pediatrics;2022-09-14