172 related articles for article (PubMed ID: 23645318)
1. Mutational analysis in podocin-associated hereditary nephrotic syndrome in Polish patients: founder effect in the Kashubian population.
Lipska BS; Balasz-Chmielewska I; Morzuch L; Wasielewski K; Vetter D; Borzecka H; Drozdz D; Firszt-Adamczyk A; Gacka E; Jarmolinski T; Ksiazek J; Kuzma-Mroczkowska E; Litwin M; Medynska A; Silska M; Szczepanska M; Tkaczyk M; Wasilewska A; Schaefer F; Zurowska A; Limon J
J Appl Genet; 2013 Aug; 54(3):327-33. PubMed ID: 23645318
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. NPHS2 p.V290M mutation in late-onset steroid-resistant nephrotic syndrome.
Kerti A; Csohány R; Szabó A; Arkossy O; Sallay P; Moriniére V; Vega-Warner V; Nyírő G; Lakatos O; Szabó T; Lipska BS; Schaefer F; Antignac C; Reusz G; Tulassay T; Tory K
Pediatr Nephrol; 2013 May; 28(5):751-7. PubMed ID: 23242530
[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 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]
6. 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]
7. 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]
8. [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]
9. 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]
10. 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]
11. 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]
12. 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]
13. NPHS2 gene mutations in azerbaijani children with steroid-resistant nephrotic syndrome.
Baylarov R; Senol O; Atan M; Berdeli A
Saudi J Kidney Dis Transpl; 2020; 31(1):144-149. PubMed ID: 32129207
[TBL] [Abstract][Full Text] [Related]
14. [Mutations in NPHS2 in familial steroid-resistant nephrotic syndrome in Southern Chinese Han ethnic group].
Fu R; Chen XM; Wang QH; Chen SP; Yu ZH; Ye LY; Ren RN; Huang J; Wang CF
Zhonghua Er Ke Za Zhi; 2008 Aug; 46(8):591-6. PubMed ID: 19099831
[TBL] [Abstract][Full Text] [Related]
15. NPHS2 mutations in steroid-resistant nephrotic syndrome: a mutation update and the associated phenotypic spectrum.
Bouchireb K; Boyer O; Gribouval O; Nevo F; Huynh-Cong E; Morinière V; Campait R; Ars E; Brackman D; Dantal J; Eckart P; Gigante M; Lipska BS; Liutkus A; Megarbane A; Mohsin N; Ozaltin F; Saleem MA; Schaefer F; Soulami K; Torra R; Garcelon N; Mollet G; Dahan K; Antignac C
Hum Mutat; 2014 Feb; 35(2):178-86. PubMed ID: 24227627
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome.
Hinkes B; Vlangos C; Heeringa S; Mucha B; Gbadegesin R; Liu J; Hasselbacher K; Ozaltin F; Hildebrandt F;
J Am Soc Nephrol; 2008 Feb; 19(2):365-71. PubMed ID: 18216321
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. NPHS2 variation in Chinese southern infants with late steroid-resistant nephrotic syndrome.
Dai Y; Yang H; Gao P; Liu WD
Ren Fail; 2014 Oct; 36(9):1395-8. PubMed ID: 25112471
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
