282 related articles for article (PubMed ID: 15500131)
1. [Congenital nephrotic syndrome].
Hattori M
Nihon Rinsho; 2004 Oct; 62(10):1861-6. PubMed ID: 15500131
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Molecular basis of steroid-resistant nephrotic syndrome.
Antignac C
Nefrologia; 2005; 25 Suppl 2():25-8. PubMed ID: 16050398
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [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]
7. 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]
8. 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]
9. 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]
10. 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]
11. [Responsible genes for proteinuria and concept of the treatment for proteinuria].
Shimizu F
Nihon Rinsho; 2004 Oct; 62(10):1800-4. PubMed ID: 15500121
[TBL] [Abstract][Full Text] [Related]
12. Congenital nephrotic syndrome of the Finnish type is not associated with the Pax-2 gene despite the promising transgenic animal model.
Kestilä M; Männikkö M; Holmberg C; Tryggvason K; Peltonen L
Genomics; 1994 Feb; 19(3):570-2. PubMed ID: 8188301
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. [The genetic background of congenital nephrotic syndrome].
Zwolińska D
Przegl Lek; 2006; 63 Suppl 3():10-1. PubMed ID: 16898476
[No Abstract] [Full Text] [Related]
16. A missense mutation in the nephrin gene impairs membrane targeting.
Shimizu J; Tanaka H; Aya K; Ito S; Sado Y; Seino Y
Am J Kidney Dis; 2002 Oct; 40(4):697-703. PubMed ID: 12324903
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Prenatal diagnosis of congenital nephrotic syndrome (CNF, NPHS1).
Kestilä M; Järvelä I
Prenat Diagn; 2003 Apr; 23(4):323-4. PubMed ID: 12673639
[No Abstract] [Full Text] [Related]
19. 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]
20. Congenital nephrotic syndrome with a novel NPHS1 mutation.
Yoshizawa C; Kobayashi Y; Ikeuchi Y; Tashiro M; Kakegawa S; Watanabe T; Goto Y; Nakanishi K; Yoshikawa N; Arakawa H
Pediatr Int; 2016 Nov; 58(11):1211-1215. PubMed ID: 27882743
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
