Genetic mutation in Egyptian children with steroid-resistant nephrotic syndrome
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference27 articles.
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3. Clinical value of NPHS2 analysis in early- and adult-onset steroid-resistant nephritic syndrome;Santín;Clin J Am Soc Nephrol,2011
4. Novel mutations in NPHS2 detected in both familial and sporadic steroid-resistant nephrotic syndrome;Karle;J Am Soc Nephrol,2002
5. Genetic causes of focal segmental glomerulosclerosis: implications for clinical practice;Rood;Nephrol Dial Transplant,2012
Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Mutational analysis of phospholipase C epsilon 1 gene in Egyptian children with steroid-resistant nephrotic syndrome;Egyptian Journal of Medical Human Genetics;2022-11-08
2. Spectrum of NPHS1 and NPHS2 variants in egyptian children with focal segmental glomerular sclerosis: identification of six novel variants and founder effect;Molecular Genetics and Genomics;2022-03-12
3. Disease-Associated Systemic Complications in Childhood Nephrotic Syndrome: A Systematic Review;International Journal of Nephrology and Renovascular Disease;2022-02
4. Mir-142-5p as an indicator of autoimmune processes in childhood idiopathic nephrotic syndrome and as a part of MicroRNAs expression panels for its diagnosis and prediction of response to steroid treatment;Molecular Immunology;2022-01
5. A descriptive study of NPHS1 and NPHS2 mutations in children with congenital nephrotic syndrome;Gene Reports;2020-09
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