427 related articles for article (PubMed ID: 10972661)
1. 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]
2. 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]
3. [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]
4. 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]
5. Role of nephrin in cell junction formation in human nephrogenesis.
Ruotsalainen V; Patrakka J; Tissari P; Reponen P; Hess M; Kestilä M; Holmberg C; Salonen R; Heikinheimo M; Wartiovaara J; Tryggvason K; Jalanko H
Am J Pathol; 2000 Dec; 157(6):1905-16. PubMed ID: 11106563
[TBL] [Abstract][Full Text] [Related]
6. Glomerular sclerosis in kidneys with congenital nephrotic syndrome (NPHS1).
Kuusniemi AM; Merenmies J; Lahdenkari AT; Holmberg C; Salmela K; Karikoski R; Rapola J; Jalanko H
Kidney Int; 2006 Oct; 70(8):1423-31. PubMed ID: 16941028
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Defective nephrin trafficking caused by missense mutations in the NPHS1 gene: insight into the mechanisms of congenital nephrotic syndrome.
Liu L; Doné SC; Khoshnoodi J; Bertorello A; Wartiovaara J; Berggren PO; Tryggvason K
Hum Mol Genet; 2001 Nov; 10(23):2637-44. PubMed ID: 11726550
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Tissue expression of nephrin in human and pig.
Kuusniemi AM; Kestilä M; Patrakka J; Lahdenkari AT; Ruotsalainen V; Holmberg C; Karikoski R; Salonen R; Tryggvason K; Jalanko H
Pediatr Res; 2004 May; 55(5):774-81. PubMed ID: 14764915
[TBL] [Abstract][Full Text] [Related]
11. [Congenital nephrotic syndrome].
Hattori M
Nihon Rinsho; 2004 Oct; 62(10):1861-6. PubMed ID: 15500131
[TBL] [Abstract][Full Text] [Related]
12. Glomerular endothelium in kidneys with congenital nephrotic syndrome of the Finnish type (NPHS1).
Kaukinen A; Kuusniemi AM; Lautenschlager I; Jalanko H
Nephrol Dial Transplant; 2008 Apr; 23(4):1224-32. PubMed ID: 18048423
[TBL] [Abstract][Full Text] [Related]
13. Detection of the Finnish-type congenital nephrotic syndrome by restriction fragment length polymorphism and dual-color oligonucleotide ligation assays.
Romppanen EL; Mononen I
Clin Chem; 2000 Jun; 46(6 Pt 1):811-6. PubMed ID: 10839769
[TBL] [Abstract][Full Text] [Related]
14. Muscular dystonia and athetosis in six patients with congenital nephrotic syndrome of the Finnish type (NPHS1).
Laakkonen H; Lönnqvist T; Uusimaa J; Qvist E; Valanne L; Nuutinen M; Ala-Houhala M; Majamaa K; Jalanko H; Holmberg C
Pediatr Nephrol; 2006 Feb; 21(2):182-9. PubMed ID: 16362719
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approach.
Gigante M; Monno F; Roberto R; Laforgia N; Assael MB; Livolti S; Caringella A; La Manna A; Masella L; Iolascon A
J Nephrol; 2002; 15(6):696-702. PubMed ID: 12495287
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome.
Machuca E; Benoit G; Nevo F; Tête MJ; Gribouval O; Pawtowski A; Brandström P; Loirat C; Niaudet P; Gubler MC; Antignac C
J Am Soc Nephrol; 2010 Jul; 21(7):1209-17. PubMed ID: 20507940
[TBL] [Abstract][Full Text] [Related]
20. Congenital nephrotic syndrome of NPHS1 associated with cardiac malformation.
Uysal B; Dönmez O; Uysal F; Akacı O; Vuruşkan BA; Berdeli A
Pediatr Int; 2015; 57(1):177-9. PubMed ID: 25711261
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]