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229 related items for PubMed ID: 15504144
1. A novel NPHS2 gene mutation in Turkish children with familial steroid-resistant nephrotic syndrome. Ozer EA, Aksu N, Erdogan H, Yavascan O, Kara O, Gribouval O, Gubler MC, Antignac C. Nephrology (Carlton); 2004 Oct; 9(5):310-2. PubMed ID: 15504144 [Abstract] [Full Text] [Related]
2. 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 [Abstract] [Full Text] [Related]
3. The heart of children with steroid-resistant nephrotic syndrome: is it all podocin? Frishberg Y, Feinstein S, Rinat C, Becker-Cohen R, Lerer I, Raas-Rothschild A, Ferber B, Nir A. J Am Soc Nephrol; 2006 Jan; 17(1):227-31. PubMed ID: 16291839 [Abstract] [Full Text] [Related]
4. [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 Jan; 63 Suppl 3():85-6. PubMed ID: 16898497 [Abstract] [Full Text] [Related]
5. NPHS2 mutations in children with steroid-resistant nephrotic syndrome. Otukesh H, Ghazanfari B, Fereshtehnejad SM, Bakhshayesh M, Hashemi M, Hoseini R, Chalian M, Salami A, Mehdipor L, Rahiminia A. Iran J Kidney Dis; 2009 Apr; 3(2):99-102. PubMed ID: 19395786 [Abstract] [Full Text] [Related]
6. 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 10; 502(2):133-7. PubMed ID: 22565185 [Abstract] [Full Text] [Related]
7. 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, Arbeitsgemeinschaft für Paediatrische Nephrologie Study Group. Pediatrics; 2007 Apr 10; 119(4):e907-19. PubMed ID: 17371932 [Abstract] [Full Text] [Related]
9. 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 10; 13(2):400-405. PubMed ID: 11805168 [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 10; 66(2):571-9. PubMed ID: 15253708 [Abstract] [Full Text] [Related]
11. Novel human pathological mutations. Gene symbol: NPHS2. Disease: steroid-resistant nephrotic syndrome. Tikhomirov E, Averyanova N, Bayazutdinova G, Voznesenskaya T, Tsygin A. Hum Genet; 2007 Dec 10; 122(5):549. PubMed ID: 18380020 [No Abstract] [Full Text] [Related]
12. 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 10; 426(1-2):177-181. PubMed ID: 27885584 [Abstract] [Full Text] [Related]
13. Analysis of NPHS2 mutations in Turkish steroid-resistant nephrotic syndrome patients. Ozçakar ZB, Cengiz FB, Cakar N, Uncu N, Kara N, Acar B, Yüksel S, Ekim M, Tekin M, Yalçinkaya F. Pediatr Nephrol; 2006 Aug 10; 21(8):1093-6. PubMed ID: 16810518 [Abstract] [Full Text] [Related]
14. TRPC6 gene variants in Turkish children with steroid-resistant nephrotic syndrome. Mir S, Yavascan O, Berdeli A, Sozeri B. Nephrol Dial Transplant; 2012 Jan 10; 27(1):205-9. PubMed ID: 21511817 [Abstract] [Full Text] [Related]
15. 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 10; 7(5):357-62. PubMed ID: 24072147 [Abstract] [Full Text] [Related]
16. 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 10; 18(5):412-6. PubMed ID: 12687458 [Abstract] [Full Text] [Related]
17. Genetics of steroid-resistant nephrotic syndrome: a review of mutation spectrum and suggested approach for genetic testing. Joshi S, Andersen R, Jespersen B, Rittig S. Acta Paediatr; 2013 Sep 10; 102(9):844-56. PubMed ID: 23772861 [Abstract] [Full Text] [Related]
18. 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 10; 22(12):2031-40. PubMed ID: 17899208 [Abstract] [Full Text] [Related]
19. 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 10; 21(1):127-133. PubMed ID: 26820844 [Abstract] [Full Text] [Related]
20. 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, Arbeitsgemeinschaft Für Pädiatrische Nephrologie Study Group. J Am Soc Nephrol; 2004 Mar 10; 15(3):722-32. PubMed ID: 14978175 [Abstract] [Full Text] [Related] Page: [Next] [New Search]