New insights from the genetic work-up in early onset nephrotic syndrome: report from a registry in western India
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00467-024-06295-8.pdf
Reference23 articles.
1. Habib R (1993) Nephrotic syndrome in the 1st year of life. Pediatr Nephrol 7:347–353
2. Gbadegesin R, Winn M, Smoyer WE (2013) Genetic testing in nephrotic syndrome: challenges and opportunities. Nat Rev Nephrol 9:179–184
3. Cil O, Besbas N, Duzova A, Topaloglu R, Peco-Antić A, Korkmaz E et al (2015) Genetic abnormalities and prognosis in patients with congenital and infantile nephrotic syndrome. Pediatr Nephrol 30:1279–1287
4. Bérody S, Heidet L, Gribouval O, Harambat J, Niaudet P, Baudouin V et al (2019) Treatment and outcome of congenital nephrotic syndrome. Nephrol Dial Transplant 34:458–467
5. Hinkes BG, Mucha B, Vlangos CN, Gbadegesin R, Liu J, Hasselbacher K et al (2007) Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2). Pediatrics 119:907–919
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