226 related articles for article (PubMed ID: 12704574)
1. 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]
2. [A genetic viewpoint of focal glomerular sclerosis: fom genes to glomerular pathophysiology [corrected]].
Aucella F; Bisceglia L; Stallone C
G Ital Nefrol; 2003; 20(4):356-67. PubMed ID: 14523896
[TBL] [Abstract][Full Text] [Related]
3. Molecular basis of steroid-resistant nephrotic syndrome.
Antignac C
Nefrologia; 2005; 25 Suppl 2():25-8. PubMed ID: 16050398
[TBL] [Abstract][Full Text] [Related]
4. [Structure and function of the glomerular filtration barrier].
Musiał K; Zwolińska D
Pol Merkur Lekarski; 2005 Mar; 18(105):317-20. PubMed ID: 15997642
[TBL] [Abstract][Full Text] [Related]
5. Molecular analysis of NPHS2 and ACTN4 genes in a series of 33 Italian patients affected by adult-onset nonfamilial focal segmental glomerulosclerosis.
Aucella F; De Bonis P; Gatta G; Muscarella LA; Vigilante M; di Giorgio G; D'Errico M; Zelante L; Stallone C; Bisceglia L
Nephron Clin Pract; 2005; 99(2):c31-6. PubMed ID: 15627790
[TBL] [Abstract][Full Text] [Related]
6. [Characterization of the NPH2 gene, coding for the glomerular protein podocin, implicated in a familial form of cortico-resistant nephrotic syndrome transmitted as an autosomal recessive].
Boute N; Roselli S; Gribouval O; Niaudet P; Gubler MC; Antignac C
Nephrologie; 2002; 23(1):35-6. PubMed ID: 11908478
[No Abstract] [Full Text] [Related]
7. Late onset of familial nephrotic syndrome associated with a compound heterozygous mutation of the podocin-encoding gene.
Ardiles LG; Carrasco AE; Carpio JD; Mezzano SA
Nephrology (Carlton); 2005 Dec; 10(6):553-6. PubMed ID: 16354237
[TBL] [Abstract][Full Text] [Related]
8. [Focal segmental glomerulosclerosis].
Yuzawa Y; Matsuo S
Nihon Rinsho; 2004 Oct; 62(10):1837-41. PubMed ID: 15500127
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Animal models of FSGS: lessons for pathogenesis and treatment.
Fogo AB
Semin Nephrol; 2003 Mar; 23(2):161-71. PubMed ID: 12704576
[TBL] [Abstract][Full Text] [Related]
11. Analysis of mutations in alpha-actinin 4 and podocin genes of patients with chronic renal failure due to sporadic focal segmental glomerulosclerosis.
Komatsuda A; Wakui H; Maki N; Kigawa A; Goto H; Ohtani H; Hamai K; Oyama Y; Makoto H; Sawada K; Imai H
Ren Fail; 2003 Jan; 25(1):87-93. PubMed ID: 12617336
[TBL] [Abstract][Full Text] [Related]
12. Molecular basis of the functional podocin-nephrin complex: mutations in the NPHS2 gene disrupt nephrin targeting to lipid raft microdomains.
Huber TB; Simons M; Hartleben B; Sernetz L; Schmidts M; Gundlach E; Saleem MA; Walz G; Benzing T
Hum Mol Genet; 2003 Dec; 12(24):3397-405. PubMed ID: 14570703
[TBL] [Abstract][Full Text] [Related]
13. Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis.
Caridi G; Bertelli R; Carrea A; Di Duca M; Catarsi P; Artero M; Carraro M; Zennaro C; Candiano G; Musante L; Seri M; Ginevri F; Perfumo F; Ghiggeri GM
J Am Soc Nephrol; 2001 Dec; 12(12):2742-2746. PubMed ID: 11729243
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. Podocyte proteins in Galloway-Mowat syndrome.
Srivastava T; Whiting JM; Garola RE; Dasouki MJ; Ruotsalainen V; Tryggvason K; Hamed R; Alon US
Pediatr Nephrol; 2001 Dec; 16(12):1022-9. PubMed ID: 11793093
[TBL] [Abstract][Full Text] [Related]
16. Direct effect of plasma permeability factors from patients with idiopatic FSGS on nephrin and podocin expression in human podocytes.
Doublier S; Musante L; Lupia E; Candiano G; Spatola T; Caridi G; Zennaro C; Carraro M; Ghiggeri GM; Camussi G
Int J Mol Med; 2005 Jul; 16(1):49-58. PubMed ID: 15942677
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. Focal segmental glomerulosclerosis in nephrotic adults: presentation, prognosis, and response to therapy of the histologic variants.
Chun MJ; Korbet SM; Schwartz MM; Lewis EJ
J Am Soc Nephrol; 2004 Aug; 15(8):2169-77. PubMed ID: 15284302
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
