201 related articles for article (PubMed ID: 24519673)
1. NPHS2 R229Q polymorphism in steroid resistant nephrotic syndrome: is it responsive to immunosuppressive therapy?
Mishra OP; Kakani N; Singh AK; Narayan G; Abhinay A; Prasad R; Batra VV
J Trop Pediatr; 2014 Jun; 60(3):231-7. PubMed ID: 24519673
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. [NPHS2 Mutation analysis study in children with steroid-resistant nephrotic syndrome].
Azocar M; Vega Á; Farfán M; Cano F
Rev Chil Pediatr; 2016; 87(1):31-6. PubMed ID: 26455708
[TBL] [Abstract][Full Text] [Related]
4. Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian children.
Dhandapani MC; Venkatesan V; Rengaswamy NB; Gowrishankar K; Ekambaram S; Sengutavan P; Perumal V
Clin Exp Nephrol; 2017 Feb; 21(1):127-133. PubMed ID: 26820844
[TBL] [Abstract][Full Text] [Related]
5. NPHS2 gene in steroid-resistant nephrotic syndrome: prevalence, clinical course, and mutational spectrum in South-West Iranian children.
Basiratnia M; Yavarian M; Torabinezhad S; Erjaee A
Iran J Kidney Dis; 2013 Sep; 7(5):357-62. PubMed ID: 24072147
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. Nucleotide variations in the NPHS2 gene in Greek children with steroid-resistant nephrotic syndrome.
Megremis S; Mitsioni A; Mitsioni AG; Fylaktou I; Kitsiou-Tzelli S; Stefanidis CJ; Kanavakis E; Traeger-Synodinos J
Genet Test Mol Biomarkers; 2009 Apr; 13(2):249-56. PubMed ID: 19371226
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome.
Büscher AK; Beck BB; Melk A; Hoefele J; Kranz B; Bamborschke D; Baig S; Lange-Sperandio B; Jungraithmayr T; Weber LT; Kemper MJ; Tönshoff B; Hoyer PF; Konrad M; Weber S;
Clin J Am Soc Nephrol; 2016 Feb; 11(2):245-53. PubMed ID: 26668027
[TBL] [Abstract][Full Text] [Related]
10. Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome.
Ruf RG; Lichtenberger A; Karle SM; Haas JP; Anacleto FE; Schultheiss M; Zalewski I; Imm A; Ruf EM; Mucha B; Bagga A; Neuhaus T; Fuchshuber A; Bakkaloglu A; Hildebrandt F;
J Am Soc Nephrol; 2004 Mar; 15(3):722-32. PubMed ID: 14978175
[TBL] [Abstract][Full Text] [Related]
11. Clinical and epidemiological assessment of steroid-resistant nephrotic syndrome associated with the NPHS2 R229Q variant.
Machuca E; Hummel A; Nevo F; Dantal J; Martinez F; Al-Sabban E; Baudouin V; Abel L; Grünfeld JP; Antignac C
Kidney Int; 2009 Apr; 75(7):727-35. PubMed ID: 19145239
[TBL] [Abstract][Full Text] [Related]
12. Mutations in NPHS2 in sporadic steroid-resistant nephrotic syndrome in Chinese children.
Yu Z; Ding J; Huang J; Yao Y; Xiao H; Zhang J; Liu J; Yang J
Nephrol Dial Transplant; 2005 May; 20(5):902-8. PubMed ID: 15769810
[TBL] [Abstract][Full Text] [Related]
13. Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome.
Gbadegesin R; Hinkes B; Vlangos C; Mucha B; Liu J; Hopcian J; Hildebrandt F
Pediatr Nephrol; 2007 Apr; 22(4):509-13. PubMed ID: 17216259
[TBL] [Abstract][Full Text] [Related]
14. Genetic mutation in Egyptian children with steroid-resistant nephrotic syndrome.
Thomas MM; Abdel-Hamid MS; Mahfouz NN; Ghobrial EE
J Formos Med Assoc; 2018 Jan; 117(1):48-53. PubMed ID: 28385484
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. The p.R229Q variant of the NPHS2 (podocin) gene in focal segmental glomerulosclerosis and steroid-resistant nephrotic syndrome: a meta-analysis.
Lu L; Wan H; Yin Y; Feng WJ; Wang M; Zou YC; Huang B; Wang DT; Shi Y; Zhao Y; Wei LB
Int Urol Nephrol; 2014 Jul; 46(7):1383-93. PubMed ID: 24715228
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Mutations in NPHS2 (podocin) in Mexican children with nephrotic syndrome who respond to standard steroid treatment.
Carrasco-Miranda JS; Garcia-Alvarez R; Sotelo-Mundo RR; Valenzuela O; Islas-Osuna MA; Sotelo-Cruz N
Genet Mol Res; 2013 Jun; 12(2):2102-7. PubMed ID: 23913389
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]