These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
153 related articles for article (PubMed ID: 34396835)
21. 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 BG; Mucha B; Vlangos CN; Gbadegesin R; Liu J; Hasselbacher K; Hangan D; Ozaltin F; Zenker M; Hildebrandt F; Pediatrics; 2007 Apr; 119(4):e907-19. PubMed ID: 17371932 [TBL] [Abstract][Full Text] [Related]
22. Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome. Ruf RG; Lichtenberger A; Karle SM; Haas JP; Anacleto FE; Schultheiss M; Zalewski I; Imm A; Ruf EM; Mucha B; Bagga A; Neuhaus T; Fuchshuber A; Bakkaloglu A; Hildebrandt F; J Am Soc Nephrol; 2004 Mar; 15(3):722-32. PubMed ID: 14978175 [TBL] [Abstract][Full Text] [Related]
23. A novel heterozygous mutation of the NPHS1 gene in a Chinese child with congenital nephrotic syndrome: A case report. Xie D; Wu J; Zhang W; Jin T; Wu P; An B; Huang S Medicine (Baltimore); 2023 Feb; 102(7):e32970. PubMed ID: 36800604 [TBL] [Abstract][Full Text] [Related]
24. Gastric duplication cyst in an infant with Finnish-type congenital nephrotic syndrome: concurrence or coincidence? Güngör T; Eroğlu FK; Kargın Çakıcı E; Yazılıtaş F; Can G; Çelikkaya E; Karakaya D; Kurt Şükür ED; Özaltın F; Yağız B; Bülbül M Acta Clin Belg; 2021 Apr; 76(2):155-157. PubMed ID: 31587616 [TBL] [Abstract][Full Text] [Related]
25. Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration. Koziell A; Grech V; Hussain S; Lee G; Lenkkeri U; Tryggvason K; Scambler P Hum Mol Genet; 2002 Feb; 11(4):379-88. PubMed ID: 11854170 [TBL] [Abstract][Full Text] [Related]
26. No evidence for genotype/phenotype correlation in NPHS1 and NPHS2 mutations. Schultheiss M; Ruf RG; Mucha BE; Wiggins R; Fuchshuber A; Lichtenberger A; Hildebrandt F Pediatr Nephrol; 2004 Dec; 19(12):1340-8. PubMed ID: 15338398 [TBL] [Abstract][Full Text] [Related]
27. NPHS1 gene mutations in children with Nephrotic Syndrome in northwest Iran. Behbahan AG; Poorshiri B; Mortazavi F; Khaniani MS; Derakhshan SM Pak J Biol Sci; 2013 Sep; 16(17):882-6. PubMed ID: 24498843 [TBL] [Abstract][Full Text] [Related]
32. Effectiveness of Supramaximal Angiotensin-converting Enzyme Inhibition in Controlling Proteinuria in Congenital Nephrotic Syndrome with Cytomegalovirus Infection and an NPHS1 Mutation. Dange N; Sathe KP; Kondekar A; Sawant V Saudi J Kidney Dis Transpl; 2023 Sep; 34(5):462-467. PubMed ID: 38995307 [TBL] [Abstract][Full Text] [Related]
33. Neonatal nephrotic presentation of a child with heterozygous NPHS1 mutation. Lemley KV Pediatr Nephrol; 2006 Jun; 21(6):864-6. PubMed ID: 16703378 [TBL] [Abstract][Full Text] [Related]
34. Timing of renal replacement therapy does not influence survival and growth in children with congenital nephrotic syndrome caused by mutations in NPHS1: data from the ESPN/ERA-EDTA Registry. Hölttä T; Bonthuis M; Van Stralen KJ; Bjerre A; Topaloglu R; Ozaltin F; Holmberg C; Harambat J; Jager KJ; Schaefer F; Groothoff JW Pediatr Nephrol; 2016 Dec; 31(12):2317-2325. PubMed ID: 27761660 [TBL] [Abstract][Full Text] [Related]
35. The etiology of congenital nephrotic syndrome: current status and challenges. Wang JJ; Mao JH World J Pediatr; 2016 May; 12(2):149-58. PubMed ID: 26961288 [TBL] [Abstract][Full Text] [Related]
36. Genetic screening in children with challenging nephrotic syndrome. Saeed B Saudi J Kidney Dis Transpl; 2020; 31(6):1189-1197. PubMed ID: 33565430 [TBL] [Abstract][Full Text] [Related]
37. Case report: Unveiling a less severe congenital nephrotic syndrome in a Rapa Nui patient with a Krall P; Rojo A; Plaza A; Canals S; Ceballos ML; Cano F; Guerrero JL Front Nephrol; 2024; 4():1379061. PubMed ID: 38808020 [TBL] [Abstract][Full Text] [Related]
38. Novel variations in NPHS1 gene in children of South Indian population and its association with primary nephrotic syndrome. Mohanapriya CD; Vettriselvi V; Nammalwar BR; Gowrishankar K; Ekambaram S; Sengutavan P; Venkatachalam P J Cell Biochem; 2018 Dec; 119(12):10143-10150. PubMed ID: 30171708 [TBL] [Abstract][Full Text] [Related]