123 related articles for article (PubMed ID: 11908478)
21. [New findings on the pathogenesis of nephrotic syndrome (review article)].
Tesar V; Zima T; Kalousová M
Sb Lek; 2002; 103(3):379-95. PubMed ID: 12688182
[TBL] [Abstract][Full Text] [Related]
22. Another autosomal recessive form of focal glomerulosclerosis with neurological findings.
Nakazato H; Hattori S; Karashima S; Kawano T; Seguchi S; Kanahori M; Endo F
Pediatr Nephrol; 2002 Jan; 17(1):16-9. PubMed ID: 11793129
[TBL] [Abstract][Full Text] [Related]
23. The heart of children with steroid-resistant nephrotic syndrome: is it all podocin?
Frishberg Y; Feinstein S; Rinat C; Becker-Cohen R; Lerer I; Raas-Rothschild A; Ferber B; Nir A
J Am Soc Nephrol; 2006 Jan; 17(1):227-31. PubMed ID: 16291839
[TBL] [Abstract][Full Text] [Related]
24. [The genetic basis of familial focal segmental glomerulosclerosis and related nephrotic syndrome].
Tsukaguchi H; Kitamura A
Nihon Jinzo Gakkai Shi; 2007; 49(2):88-97. PubMed ID: 17375615
[No Abstract] [Full Text] [Related]
25. [Heterozygotic mutation in NPHS2 gene as a cause of familial steroid resistant nephrotic syndrome in two siblings--case report].
Drozdz D; Pietrzyk JA; Wierzchowska-Słowiaczek E; Sancewicz-Pach K; Antignac C; Miezyński W
Przegl Lek; 2006; 63 Suppl 3():85-6. PubMed ID: 16898497
[TBL] [Abstract][Full Text] [Related]
26. Pediatric nephrotic syndrome: from the simple to the complex.
Lane JC; Kaskel FJ
Semin Nephrol; 2009 Jul; 29(4):389-98. PubMed ID: 19615560
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Podocin inactivation in mature kidneys causes focal segmental glomerulosclerosis and nephrotic syndrome.
Mollet G; Ratelade J; Boyer O; Muda AO; Morisset L; Lavin TA; Kitzis D; Dallman MJ; Bugeon L; Hubner N; Gubler MC; Antignac C; Esquivel EL
J Am Soc Nephrol; 2009 Oct; 20(10):2181-9. PubMed ID: 19713307
[TBL] [Abstract][Full Text] [Related]
29. A novel NPHS2 gene mutation in Turkish children with familial steroid-resistant nephrotic syndrome.
Ozer EA; Aksu N; Erdogan H; Yavascan O; Kara O; Gribouval O; Gubler MC; Antignac C
Nephrology (Carlton); 2004 Oct; 9(5):310-2. PubMed ID: 15504144
[TBL] [Abstract][Full Text] [Related]
30. Getting a foothold in nephrotic syndrome.
Somlo S; Mundel P
Nat Genet; 2000 Apr; 24(4):333-5. PubMed ID: 10742089
[No Abstract] [Full Text] [Related]
31. Structural characterization and mutational assessment of podocin - a novel drug target to nephrotic syndrome - an in silico approach.
Tabassum A; Rajeshwari T; Soni N; Raju DS; Yadav M; Nayarisseri A; Jahan P
Interdiscip Sci; 2014 Mar; 6(1):32-9. PubMed ID: 24464702
[TBL] [Abstract][Full Text] [Related]
32. Specific podocin mutations determine age of onset of nephrotic syndrome all the way into adult life.
Hildebrandt F; Heeringa SF
Kidney Int; 2009 Apr; 75(7):669-71. PubMed ID: 19282856
[TBL] [Abstract][Full Text] [Related]
33. Mutations in NPHS2 in sporadic steroid-resistant nephrotic syndrome in Chinese children.
Yu Z; Ding J; Huang J; Yao Y; Xiao H; Zhang J; Liu J; Yang J
Nephrol Dial Transplant; 2005 May; 20(5):902-8. PubMed ID: 15769810
[TBL] [Abstract][Full Text] [Related]
34. Novel human pathological mutations. Gene symbol: NPHS2. Disease: steroid-resistant nephrotic syndrome.
Tikhomirov E; Averyanova N; Bayazutdinova G; Voznesenskaya T; Tsygin A
Hum Genet; 2007 Dec; 122(5):549. PubMed ID: 18380020
[No Abstract] [Full Text] [Related]
35. Mechanisms of disease: focal segmental glomerulosclerosis.
Meyrier A
Nat Clin Pract Nephrol; 2005 Nov; 1(1):44-54. PubMed ID: 16932363
[TBL] [Abstract][Full Text] [Related]
36. [Nephrotic syndrome in childhood].
Reusz G; Szabó A; Fekete A
Orv Hetil; 2006 Nov; 147(47):2251-60. PubMed ID: 17380687
[TBL] [Abstract][Full Text] [Related]
37. Podocin-related mechanisms in posttransplant [corrected] recurrence of focal segmental glomerulosclerosis [corrected].
Caridi G; Dagnino M; Sanna-Cherchi S; Perfumo F; Ghiggeri GM
Transplant Proc; 2006 Dec; 38(10):3486-90. PubMed ID: 17175312
[TBL] [Abstract][Full Text] [Related]
38. A disease-causing mutation illuminates the protein membrane topology of the kidney-expressed prohibitin homology (PHB) domain protein podocin.
Schurek EM; Völker LA; Tax J; Lamkemeyer T; Rinschen MM; Ungrue D; Kratz JE; Sirianant L; Kunzelmann K; Chalfie M; Schermer B; Benzing T; Höhne M
J Biol Chem; 2014 Apr; 289(16):11262-11271. PubMed ID: 24596097
[TBL] [Abstract][Full Text] [Related]
39. Glomerular sclerosis in transgenic mice: the Mpv-17 gene and its human homologue.
Weiher H
Adv Nephrol Necker Hosp; 1993; 22():37-42. PubMed ID: 8427063
[No Abstract] [Full Text] [Related]
40. Two novel polymorphisms (c954T>C and c1038A>G) in exon8 of NPHS2 gene identified in Taiwan Chinese.
Wu MC; Wu JY; Lee CC; Tsai CH; Tsai FJ
Hum Mutat; 2001 Mar; 17(3):237. PubMed ID: 11241850
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]