256 related articles for article (PubMed ID: 18058136)
21. Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome.
Büscher AK; Kranz B; Büscher R; Hildebrandt F; Dworniczak B; Pennekamp P; Kuwertz-Bröking E; Wingen AM; John U; Kemper M; Monnens L; Hoyer PF; Weber S; Konrad M
Clin J Am Soc Nephrol; 2010 Nov; 5(11):2075-84. PubMed ID: 20798252
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. 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]
25. WT-1 and NPHS2 mutation analysis in patients with non-familial steroid-resistant focal-segmental glomerulosclerosis.
Löwik MM; Levtchenko EN; Monnens LA; van den Heuvel LP
Clin Nephrol; 2003 Feb; 59(2):143-6. PubMed ID: 12608558
[TBL] [Abstract][Full Text] [Related]
26. Mutational spectrum and novel candidate genes in Chinese children with sporadic steroid-resistant nephrotic syndrome.
Li J; Wang L; Wan L; Lin T; Zhao W; Cui H; Li H; Cao L; Wu J; Zhang T
Pediatr Res; 2019 May; 85(6):816-821. PubMed ID: 30712057
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Wilms' tumour 1 gene mutations in south Indian children with steroid-resistant nephrotic syndrome.
Kumar AS; Srilakshmi R; Karthickeyan S; Balakrishnan K; Padmaraj R; Senguttuvan P
Indian J Med Res; 2016 Aug; 144(2):276-280. PubMed ID: 27934809
[TBL] [Abstract][Full Text] [Related]
29. mRNA sequencing of a novel NPHS2 intronic mutation in a child with focal and segmental glomerulosclerosis.
Benetti E; Caridi G; Centi S; Vella MD; Ghiggeri GM; Artifoni L; Murer L
Saudi J Kidney Dis Transpl; 2014 Jul; 25(4):854-7. PubMed ID: 24969201
[TBL] [Abstract][Full Text] [Related]
30. Clinical course and NPHS2 analysis in patients with late steroid-resistant nephrotic syndrome.
Schwaderer P; Knüppel T; Konrad M; Mehls O; Schärer K; Schaefer F; Weber S
Pediatr Nephrol; 2008 Feb; 23(2):251-6. PubMed ID: 18000687
[TBL] [Abstract][Full Text] [Related]
31. Characterization of NPHS2 gene polymorphisms associated to steroid resistance nephrotic syndrome in Indian children.
Joshi BB; Mistry KN; Gang S; Koringa PG; Joshi CG
Gene; 2017 Sep; 628():134-140. PubMed ID: 28712774
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype.
Gigante M; Caridi G; Montemurno E; Soccio M; d'Apolito M; Cerullo G; Aucella F; Schirinzi A; Emma F; Massella L; Messina G; De Palo T; Ranieri E; Ghiggeri GM; Gesualdo L
Clin J Am Soc Nephrol; 2011 Jul; 6(7):1626-34. PubMed ID: 21734084
[TBL] [Abstract][Full Text] [Related]
34. TRPC6 and NPHS2 gene variants in adult patients with steroid-resistant nephrotic syndrome in North-West of Iran.
Zununi Vahed S; Moghaddas Sani H; Haghi M; Mohajel Shoja M; Ardalan M
Mol Biol Rep; 2019 Dec; 46(6):6339-6344. PubMed ID: 31529341
[TBL] [Abstract][Full Text] [Related]
35. Familial focal segmental glomerulosclerosis (FSGS) in a Nigerian family and exclusion of mutations in NPHS2,WT1 and APOL1.
Anochie IC; Eke FU; Okpere AN
West Afr J Med; 2012; 31(4):273-6. PubMed ID: 23468032
[TBL] [Abstract][Full Text] [Related]
36. Urinary cytokines and steroid responsiveness in idiopathic nephrotic syndrome of childhood.
Woroniecki RP; Shatat IF; Supe K; Du Z; Kaskel FJ
Am J Nephrol; 2008; 28(1):83-90. PubMed ID: 17914249
[TBL] [Abstract][Full Text] [Related]
37. Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome.
Ruf RG; Schultheiss M; Lichtenberger A; Karle SM; Zalewski I; Mucha B; Everding AS; Neuhaus T; Patzer L; Plank C; Haas JP; Ozaltin F; Imm A; Fuchshuber A; Bakkaloglu A; Hildebrandt F;
Kidney Int; 2004 Aug; 66(2):564-70. PubMed ID: 15253707
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. A novel mutation of NPHS2 identified in a Chinese family.
Yu Z; Ding J; Guan N; Shi Y; Zhang J; Huang J; Yao Y; Yang J
Pediatr Nephrol; 2004 Nov; 19(11):1285-9. PubMed ID: 15322893
[TBL] [Abstract][Full Text] [Related]
40. Follow-up of steroid-resistant nephrotic syndrome: tubular proteinuria and enzymuria.
Vallés P; Peralta M; Carrizo L; Martin L; Principi I; Gonzalez A; Manucha W
Pediatr Nephrol; 2000 Dec; 15(3-4):252-8. PubMed ID: 11149121
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
