264 related articles for article (PubMed ID: 16354237)
1. 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]
2. [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]
3. 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]
4. Clinical value of NPHS2 analysis in early- and adult-onset steroid-resistant nephrotic syndrome.
Santín S; Tazón-Vega B; Silva I; Cobo MÁ; Giménez I; Ruíz P; García-Maset R; Ballarín J; Torra R; Ars E;
Clin J Am Soc Nephrol; 2011 Feb; 6(2):344-54. PubMed ID: 20947785
[TBL] [Abstract][Full Text] [Related]
5. NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome.
Berdeli A; Mir S; Yavascan O; Serdaroglu E; Bak M; Aksu N; Oner A; Anarat A; Donmez O; Yildiz N; Sever L; Tabel Y; Dusunsel R; Sonmez F; Cakar N
Pediatr Nephrol; 2007 Dec; 22(12):2031-40. PubMed ID: 17899208
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclerosis.
Löwik M; Levtchenko E; Westra D; Groenen P; Steenbergen E; Weening J; Lilien M; Monnens L; van den Heuvel L
Nephrol Dial Transplant; 2008 Oct; 23(10):3146-51. PubMed ID: 18443213
[TBL] [Abstract][Full Text] [Related]
9. NPHS2 mutations in adult patients with primary focal segmental glomerulosclerosis.
Monteiro EJ; Pereira AC; Pereira AB; Krieger JE; Mastroianni-Kirsztajn G
J Nephrol; 2006; 19(3):366-71. PubMed ID: 16874699
[TBL] [Abstract][Full Text] [Related]
10. R229Q polymorphism of NPHS2 gene in patients with late-onset steroid-resistance nephrotic syndrome: a preliminary study.
Fotouhi N; Ardalan M; Jabbarpour Bonyadi M; Abdolmohammadi R; Kamalifar A; Nasri H; Einollahi B
Iran J Kidney Dis; 2013 Sep; 7(5):399-403. PubMed ID: 24072153
[TBL] [Abstract][Full Text] [Related]
11. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome.
Boute N; Gribouval O; Roselli S; Benessy F; Lee H; Fuchshuber A; Dahan K; Gubler MC; Niaudet P; Antignac C
Nat Genet; 2000 Apr; 24(4):349-54. PubMed ID: 10742096
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. Focal segmental glomerulosclerosis: recent advances.
Pollak MR
Curr Opin Nephrol Hypertens; 2008 Mar; 17(2):138-42. PubMed ID: 18277145
[TBL] [Abstract][Full Text] [Related]
14. Broadening the spectrum of diseases related to podocin mutations.
Caridi G; Bertelli R; Di Duca M; Dagnino M; Emma F; Onetti Muda A; Scolari F; Miglietti N; Mazzucco G; Murer L; Carrea A; Massella L; Rizzoni G; Perfumo F; Ghiggeri GM
J Am Soc Nephrol; 2003 May; 14(5):1278-86. PubMed ID: 12707396
[TBL] [Abstract][Full Text] [Related]
15. NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review.
Franceschini N; North KE; Kopp JB; McKenzie L; Winkler C
Genet Med; 2006 Feb; 8(2):63-75. PubMed ID: 16481888
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Molecular basis of steroid-resistant nephrotic syndrome.
Antignac C
Nefrologia; 2005; 25 Suppl 2():25-8. PubMed ID: 16050398
[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. CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS).
Gigante M; Pontrelli P; Montemurno E; Roca L; Aucella F; Penza R; Caridi G; Ranieri E; Ghiggeri GM; Gesualdo L
Nephrol Dial Transplant; 2009 Jun; 24(6):1858-64. PubMed ID: 19131354
[TBL] [Abstract][Full Text] [Related]
20. [A novel mutation of NPHS2 identified in a Chinese family with steroid-resistant nephrotic syndrome].
Yu ZH; Ding J; Guan N; Shi Y; Zhang JJ; Huang JP; Yao Y; Yang JY
Zhonghua Er Ke Za Zhi; 2004 Feb; 42(2):108-12. PubMed ID: 15059485
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
