224 related articles for article (PubMed ID: 19956976)
1. Analysis of recessive CD2AP and ACTN4 mutations in steroid-resistant nephrotic syndrome.
Benoit G; Machuca E; Nevo F; Gribouval O; Lepage D; Antignac C
Pediatr Nephrol; 2010 Mar; 25(3):445-51. PubMed ID: 19956976
[TBL] [Abstract][Full Text] [Related]
2. Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa.
Nandlal L; Winkler CA; Bhimma R; Cho S; Nelson GW; Haripershad S; Naicker T
Eur J Pediatr; 2022 Oct; 181(10):3595-3606. PubMed ID: 35920919
[TBL] [Abstract][Full Text] [Related]
3. Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome.
Santín S; Bullich G; Tazón-Vega B; García-Maset R; Giménez I; Silva I; Ruíz P; Ballarín J; Torra R; Ars E
Clin J Am Soc Nephrol; 2011 May; 6(5):1139-48. PubMed ID: 21415313
[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. Mutations in NPHS2 encoding podocin are a prevalent cause of steroid-resistant nephrotic syndrome among Israeli-Arab children.
Frishberg Y; Rinat C; Megged O; Shapira E; Feinstein S; Raas-Rothschild A
J Am Soc Nephrol; 2002 Feb; 13(2):400-405. PubMed ID: 11805168
[TBL] [Abstract][Full Text] [Related]
6. Novel NPHS2 variant in patients with familial steroid-resistant nephrotic syndrome with early onset, slow progression and dominant inheritance pattern.
Suvanto M; Patrakka J; Jahnukainen T; Sjöström PM; Nuutinen M; Arikoski P; Kataja J; Kestilä M; Jalanko H
Clin Exp Nephrol; 2017 Aug; 21(4):677-684. PubMed ID: 27573339
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. A Systematic Analysis of Major Susceptible Genes in Childhood-onset Steroid-resistant Nephrotic Syndrome.
Li Y; He Q; Wang Y; Dang X; Wu X; Li X; Shuai L; Yi Z
Ann Clin Lab Sci; 2019 May; 49(3):330-337. PubMed ID: 31308032
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.
Weber S; Gribouval O; Esquivel EL; Morinière V; Tête MJ; Legendre C; Niaudet P; Antignac C
Kidney Int; 2004 Aug; 66(2):571-9. PubMed ID: 15253708
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. WT1 and NPHS2 gene mutation analysis and clinical management of steroid-resistant nephrotic syndrome.
Ramanathan AS; Vijayan M; Rajagopal S; Rajendiran P; Senguttuvan P
Mol Cell Biochem; 2017 Feb; 426(1-2):177-181. PubMed ID: 27885584
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Identification of genetic causes for sporadic steroid-resistant nephrotic syndrome in adults.
Gribouval O; Boyer O; Hummel A; Dantal J; Martinez F; Sberro-Soussan R; Etienne I; Chauveau D; Delahousse M; Lionet A; Allard J; Pouteil Noble C; Tête MJ; Heidet L; Antignac C; Servais A
Kidney Int; 2018 Nov; 94(5):1013-1022. PubMed ID: 30348286
[TBL] [Abstract][Full Text] [Related]
15. In vivo expression of podocyte slit diaphragm-associated proteins in nephrotic patients with NPHS2 mutation.
Zhang SY; Marlier A; Gribouval O; Gilbert T; Heidet L; Antignac C; Gubler MC
Kidney Int; 2004 Sep; 66(3):945-54. PubMed ID: 15327385
[TBL] [Abstract][Full Text] [Related]
16. The relationship among nephrin, podocin, CD2AP, and alpha-actinin might not be a true 'interaction' in podocyte.
Fan Q; Xing Y; Ding J; Guan N; Zhang J
Kidney Int; 2006 Apr; 69(7):1207-15. PubMed ID: 16501493
[TBL] [Abstract][Full Text] [Related]
17. Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity.
Bullich G; Trujillano D; Santín S; Ossowski S; Mendizábal S; Fraga G; Madrid Á; Ariceta G; Ballarín J; Torra R; Estivill X; Ars E
Eur J Hum Genet; 2015 Sep; 23(9):1192-9. PubMed ID: 25407002
[TBL] [Abstract][Full Text] [Related]
18. Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndrome.
Lovric S; Fang H; Vega-Warner V; Sadowski CE; Gee HY; Halbritter J; Ashraf S; Saisawat P; Soliman NA; Kari JA; Otto EA; Hildebrandt F;
Clin J Am Soc Nephrol; 2014 Jun; 9(6):1109-16. PubMed ID: 24742477
[TBL] [Abstract][Full Text] [Related]
19. NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children.
Maruyama K; Iijima K; Ikeda M; Kitamura A; Tsukaguchi H; Yoshiya K; Hoshii S; Wada N; Uemura O; Satomura K; Honda M; Yoshikawa N
Pediatr Nephrol; 2003 May; 18(5):412-6. PubMed ID: 12687458
[TBL] [Abstract][Full Text] [Related]
20. Mutational analysis of the PLCE1 gene in steroid resistant nephrotic syndrome.
Boyer O; Benoit G; Gribouval O; Nevo F; Pawtowski A; Bilge I; Bircan Z; Deschênes G; Guay-Woodford LM; Hall M; Macher MA; Soulami K; Stefanidis CJ; Weiss R; Loirat C; Gubler MC; Antignac C
J Med Genet; 2010 Jul; 47(7):445-52. PubMed ID: 20591883
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
