Phenotype, genotype, and clinical outcome of Taiwanese with congenital nephrotic syndrome

Author:

Tseng Min-Hua,Lin Shih-Hua,Fan Wen-Lang,Wu Ta-Wei,Lin Shuan-Pei,Ding Jhao-Jhuang,Tsai I-JungORCID,Tsai Jeng-Daw

Funder

Chang Gung Memorial Hospital

Publisher

Elsevier BV

Subject

General Medicine

Reference34 articles.

1. Management of congenital nephrotic syndrome of the Finnish type;Holmberg;Pediatr Nephrol,1995

2. Congenital nephrotic syndrome;Jalanko;Pediatr Nephrol,2009

3. Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1 , NPHS2 , WT1 , and LAMB2);Hinkes;Pediatrics,2007

4. The podocyte as a target: cyclosporin A in the management of the nephrotic syndrome caused by WT1 mutations;Stefanidis;Eur J Pediatr,2011

5. Genetic testing in steroid-resistant nephrotic syndrome: why, who, when and how? Pediatric Nephrology [Internet];Preston,2017

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