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4. Genetic kidney diseases disclose the pathogenesis of proteinuria. Jalanko H; Patrakka J; Tryggvason K; Holmberg C Ann Med; 2001 Nov; 33(8):526-33. PubMed ID: 11730159 [TBL] [Abstract][Full Text] [Related]
5. Genetics of the nephrotic syndrome. Salomon R; Gubler MC; Niaudet P Curr Opin Pediatr; 2000 Apr; 12(2):129-34. PubMed ID: 10763762 [TBL] [Abstract][Full Text] [Related]
6. Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients. Patrakka J; Kestilä M; Wartiovaara J; Ruotsalainen V; Tissari P; Lenkkeri U; Männikkö M; Visapää I; Holmberg C; Rapola J; Tryggvason K; Jalanko H Kidney Int; 2000 Sep; 58(3):972-80. PubMed ID: 10972661 [TBL] [Abstract][Full Text] [Related]
7. Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome. Sako M; Nakanishi K; Obana M; Yata N; Hoshii S; Takahashi S; Wada N; Takahashi Y; Kaku Y; Satomura K; Ikeda M; Honda M; Iijima K; Yoshikawa N Kidney Int; 2005 Apr; 67(4):1248-55. PubMed ID: 15780077 [TBL] [Abstract][Full Text] [Related]
8. Expanding the clinical spectrum of congenital nephrotic syndrome caused by NPHS1 mutations. Godefroid N; Dahan K Nephrol Dial Transplant; 2010 Sep; 25(9):2837-9. PubMed ID: 20650908 [No Abstract] [Full Text] [Related]
9. Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome. Beltcheva O; Martin P; Lenkkeri U; Tryggvason K Hum Mutat; 2001 May; 17(5):368-73. PubMed ID: 11317351 [TBL] [Abstract][Full Text] [Related]
10. Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome. Heeringa SF; Vlangos CN; Chernin G; Hinkes B; Gbadegesin R; Liu J; Hoskins BE; Ozaltin F; Hildebrandt F; Nephrol Dial Transplant; 2008 Nov; 23(11):3527-33. PubMed ID: 18503012 [TBL] [Abstract][Full Text] [Related]
11. NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. Guaragna MS; Cleto TL; Souza ML; Lutaif AC; de Castro LC; Penido MG; Maciel-Guerra AT; Belangero VM; Guerra-Junior G; De Mello MP Nephrology (Carlton); 2016 Sep; 21(9):753-7. PubMed ID: 26560236 [TBL] [Abstract][Full Text] [Related]
12. A comprehensive analysis of NPHS1 gene mutations in patients with sporadic focal segmental glomerulosclerosis. Zhuo L; Huang L; Yang Z; Li G; Wang L BMC Med Genet; 2019 Jun; 20(1):111. PubMed ID: 31216994 [TBL] [Abstract][Full Text] [Related]
14. The genetic basis of FSGS and steroid-resistant nephrosis. Pollak MR Semin Nephrol; 2003 Mar; 23(2):141-6. PubMed ID: 12704574 [TBL] [Abstract][Full Text] [Related]
15. Mutation analysis of NPHS1 in a worldwide cohort of congenital nephrotic syndrome patients. Ovunc B; Ashraf S; Vega-Warner V; Bockenhauer D; Elshakhs NA; Joseph M; Hildebrandt F; Nephron Clin Pract; 2012; 120(3):c139-46. PubMed ID: 22584503 [TBL] [Abstract][Full Text] [Related]
16. Genetic basis of nephrotic syndrome--review. Obeidová H; Merta M; Reiterová J; Maixnerová D; Stekrová J; Rysavá R; Tesar V Prague Med Rep; 2006; 107(1):5-16. PubMed ID: 16752799 [TBL] [Abstract][Full Text] [Related]
17. Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS). Schoeb DS; Chernin G; Heeringa SF; Matejas V; Held S; Vega-Warner V; Bockenhauer D; Vlangos CN; Moorani KN; Neuhaus TJ; Kari JA; MacDonald J; Saisawat P; Ashraf S; Ovunc B; Zenker M; Hildebrandt F; Nephrol Dial Transplant; 2010 Sep; 25(9):2970-6. PubMed ID: 20172850 [TBL] [Abstract][Full Text] [Related]
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19. 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]