260 related articles for article (PubMed ID: 21125408)
1. Novel mutations in steroid-resistant nephrotic syndrome diagnosed in Tunisian children.
Mbarek IB; Abroug S; Omezzine A; Pawtowski A; Gubler MC; Bouslama A; Harbi A; Antignac C
Pediatr Nephrol; 2011 Feb; 26(2):241-9. PubMed ID: 21125408
[TBL] [Abstract][Full Text] [Related]
2. Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).
Hinkes BG; Mucha B; Vlangos CN; Gbadegesin R; Liu J; Hasselbacher K; Hangan D; Ozaltin F; Zenker M; Hildebrandt F;
Pediatrics; 2007 Apr; 119(4):e907-19. PubMed ID: 17371932
[TBL] [Abstract][Full Text] [Related]
3. Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis - a single-centre experience.
Bińczak-Kuleta A; Rubik J; Litwin M; Ryder M; Lewandowska K; Taryma-Leśniak O; Clark JS; Grenda R; Ciechanowicz A
Bosn J Basic Med Sci; 2014 May; 14(2):89-93. PubMed ID: 24856380
[TBL] [Abstract][Full Text] [Related]
4. Gene mutation analysis in 12 Chinese children with congenital nephrotic syndrome.
Li GM; Cao Q; Shen Q; Sun L; Zhai YH; Liu HM; An Y; Xu H
BMC Nephrol; 2018 Dec; 19(1):382. PubMed ID: 30594156
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Genetic screening in children with challenging nephrotic syndrome.
Saeed B
Saudi J Kidney Dis Transpl; 2020; 31(6):1189-1197. PubMed ID: 33565430
[TBL] [Abstract][Full Text] [Related]
7. The Role of p.Ser1105Ser (in
Thi Kim Lien N; Van Dem P; Thu Huong N; Minh Dien T; Thi Thu Thuy T; Van Tung N; Huy Hoang N; Thi Quynh Huong N
Medicina (Kaunas); 2019 Apr; 55(4):. PubMed ID: 31013750
[No Abstract] [Full Text] [Related]
8. A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.
Abid A; Khaliq S; Shahid S; Lanewala A; Mubarak M; Hashmi S; Kazi J; Masood T; Hafeez F; Naqvi SA; Rizvi SA; Mehdi SQ
Gene; 2012 Jul; 502(2):133-7. PubMed ID: 22565185
[TBL] [Abstract][Full Text] [Related]
9. NPHS2 mutations account for only 15% of nephrotic syndrome cases.
Guaragna MS; Lutaif AC; Piveta CS; Souza ML; de Souza SR; Henriques TB; Maciel-Guerra AT; Belangero VM; Guerra-Junior G; De Mello MP
BMC Med Genet; 2015 Sep; 16():88. PubMed ID: 26420286
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome.
Machuca E; Benoit G; Nevo F; Tête MJ; Gribouval O; Pawtowski A; Brandström P; Loirat C; Niaudet P; Gubler MC; Antignac C
J Am Soc Nephrol; 2010 Jul; 21(7):1209-17. PubMed ID: 20507940
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Genetic abnormalities and prognosis in patients with congenital and infantile nephrotic syndrome.
Cil O; Besbas N; Duzova A; Topaloglu R; Peco-Antić A; Korkmaz E; Ozaltin F
Pediatr Nephrol; 2015 Aug; 30(8):1279-87. PubMed ID: 25720465
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. Genetic diagnosis of steroid-resistant nephrotic syndrome in a longitudinal collection of Czech and Slovak patients: a high proportion of causative variants in NUP93.
Bezdíčka M; Štolbová Š; Seeman T; Cinek O; Malina M; Šimánková N; Průhová Š; Zieg J
Pediatr Nephrol; 2018 Aug; 33(8):1347-1363. PubMed ID: 29869118
[TBL] [Abstract][Full Text] [Related]
18. Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome.
Wang F; Zhang Y; Mao J; Yu Z; Yi Z; Yu L; Sun J; Wei X; Ding F; Zhang H; Xiao H; Yao Y; Tan W; Lovric S; Ding J; Hildebrandt F
Pediatr Nephrol; 2017 Jul; 32(7):1181-1192. PubMed ID: 28204945
[TBL] [Abstract][Full Text] [Related]
19. Genetic forms of nephrotic syndrome: a single-center experience in Brussels.
Ismaili K; Pawtowski A; Boyer O; Wissing KM; Janssen F; Hall M
Pediatr Nephrol; 2009 Feb; 24(2):287-94. PubMed ID: 18709391
[TBL] [Abstract][Full Text] [Related]
20. Screening of the
Abid A; Shahid S; Shakoor M; Lanewala AA; Hashmi S; Khaliq S
Front Genet; 2018; 9():214. PubMed ID: 30013592
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
