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.
241 related articles for article (PubMed ID: 24682440)
1. Congenital nephrotic syndrome and recurrence of proteinuria after renal transplantation. Holmberg C; Jalanko H Pediatr Nephrol; 2014 Dec; 29(12):2309-17. PubMed ID: 24682440 [TBL] [Abstract][Full Text] [Related]
2. Plasma exchange and retransplantation in recurrent nephrosis of patients with congenital nephrotic syndrome of the Finnish type (NPHS1). Kuusniemi AM; Qvist E; Sun Y; Patrakka J; Rönnholm K; Karikoski R; Jalanko H Transplantation; 2007 May; 83(10):1316-23. PubMed ID: 17519780 [TBL] [Abstract][Full Text] [Related]
3. Recurrence of nephrotic syndrome in kidney grafts of patients with congenital nephrotic syndrome of the Finnish type: role of nephrin. Patrakka J; Ruotsalainen V; Reponen P; Qvist E; Laine J; Holmberg C; Tryggvason K; Jalanko H Transplantation; 2002 Feb; 73(3):394-403. PubMed ID: 11884936 [TBL] [Abstract][Full Text] [Related]
4. Recurrence of proteinuria following renal transplantation in congenital nephrotic syndrome of the Finnish type. Srivastava T; Garola RE; Kestila M; Tryggvason K; Ruotsalainen V; Sharma M; Savin VJ; Jalanko H; Warady BA Pediatr Nephrol; 2006 May; 21(5):711-8. PubMed ID: 16518627 [TBL] [Abstract][Full Text] [Related]
5. Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome. Carraro M; Caridi G; Bruschi M; Artero M; Bertelli R; Zennaro C; Musante L; Candiano G; Perfumo F; Ghiggeri GM J Am Soc Nephrol; 2002 Jul; 13(7):1946-52. PubMed ID: 12089392 [TBL] [Abstract][Full Text] [Related]
6. Genetic forms of nephrotic syndrome. Niaudet P Pediatr Nephrol; 2004 Dec; 19(12):1313-8. PubMed ID: 15503167 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Rituximab treatment for recurrence of nephrotic syndrome in a pediatric patient after renal transplantation for congenital nephrotic syndrome of Finnish type. Chaudhuri A; Kambham N; Sutherland S; Grimm P; Alexander S; Concepcion W; Sarwal M; Wong C Pediatr Transplant; 2012 Aug; 16(5):E183-7. PubMed ID: 21672106 [TBL] [Abstract][Full Text] [Related]
10. Recurrence of nephrotic syndrome after transplantation in CNF is due to autoantibodies to nephrin. Wang SX; Ahola H; Palmen T; Solin ML; Luimula P; Holthöfer H Exp Nephrol; 2001; 9(5):327-31. PubMed ID: 11549850 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. NPHS2 mutation associated with recurrence of proteinuria after transplantation. Billing H; Müller D; Ruf R; Lichtenberger A; Hildebrandt F; August C; Querfeld U; Haffner D Pediatr Nephrol; 2004 May; 19(5):561-4. PubMed ID: 15015071 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. The podocin mutation R229Q and early recurrence (within the first year) of glomerular disease after renal transplantation. Mohey H; Thibaudin L; Laurent B; Berthoux F Ann Transplant; 2013 Aug; 18():436-42. PubMed ID: 23982418 [TBL] [Abstract][Full Text] [Related]
20. [Congenital nephrotic syndrome of the Finnish type--key to the mechanisms of proteinuria]. Holmberg C; Jalanko H Duodecim; 2011; 127(10):1017-25. PubMed ID: 21696001 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]