Heterozygous NPHS1 or NPHS2 mutations in responsive nephrotic syndrome and the multifactorial origin of proteinuria
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference4 articles.
1. Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS);Lahdenkari;Kidney Int,2004
2. Broadening the spectrum of diseases related to podocin mutations;Caridi;J Am Soc Nephrol,2003
3. Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome;Ruf;J Am Soc Nephrol,2004
4. Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome;Carraro;J Am Soc Nephrol,2002
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2. Molecular stratification of idiopathic nephrotic syndrome;Nature Reviews Nephrology;2019-10-25
3. Post-transplant recurrence of steroid resistant nephrotic syndrome in children: the Italian experience;Journal of Nephrology;2019-10-15
4. Deriving and understanding the risk of post-transplant recurrence of nephrotic syndrome in the light of current molecular and genetic advances;Pediatric Nephrology;2017-10-11
5. Proteinuria in AMPD2-deficient mice;Genes to Cells;2011-12-29
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