171 related articles for article (PubMed ID: 15042551)
1. Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocin.
Caridi G; Berdeli A; Dagnino M; Di Duca M; Mir S; Cura A; Ravazzolo R; Ghiggeri GM
Am J Kidney Dis; 2004 Apr; 43(4):727-32. PubMed ID: 15042551
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Broadening the spectrum of diseases related to podocin mutations.
Caridi G; Bertelli R; Di Duca M; Dagnino M; Emma F; Onetti Muda A; Scolari F; Miglietti N; Mazzucco G; Murer L; Carrea A; Massella L; Rizzoni G; Perfumo F; Ghiggeri GM
J Am Soc Nephrol; 2003 May; 14(5):1278-86. PubMed ID: 12707396
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. The podocin V260E mutation predicts steroid resistant nephrotic syndrome in black South African children with focal segmental glomerulosclerosis.
Govender MA; Fabian J; Gottlich E; Levy C; Moonsamy G; Maher H; Winkler CA; Ramsay M
Commun Biol; 2019; 2():416. PubMed ID: 31754646
[TBL] [Abstract][Full Text] [Related]
8. Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration.
Koziell A; Grech V; Hussain S; Lee G; Lenkkeri U; Tryggvason K; Scambler P
Hum Mol Genet; 2002 Feb; 11(4):379-88. PubMed ID: 11854170
[TBL] [Abstract][Full Text] [Related]
9. Late onset of familial nephrotic syndrome associated with a compound heterozygous mutation of the podocin-encoding gene.
Ardiles LG; Carrasco AE; Carpio JD; Mezzano SA
Nephrology (Carlton); 2005 Dec; 10(6):553-6. PubMed ID: 16354237
[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. 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]
12. 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]
13. 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]
14. 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]
15. 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]
16. 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]
17. Three siblings with steroid-resistant nephrotic syndrome: new NPHS2 mutations in a Turkish family.
Ekim M; Ozçakar ZB; Acar B; Yüksel S; Yalçnkaya F; Tulunay O; Ensari A; Erbay B
Am J Kidney Dis; 2004 Aug; 44(2):e22-24. PubMed ID: 15264208
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
