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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
1980 1
1985 1
1989 2
1990 1
1991 1
1994 1
2000 2
2001 2
2002 5
2003 5
2004 14
2005 7
2006 9
2007 9
2008 10
2009 6
2010 9
2011 9
2012 7
2013 10
2014 17
2015 12
2016 9
2017 23
2018 34
2019 39
2020 32
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Similar Articles for PMID: 14978175

240 results
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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. Ruf RG, et al. J Am Soc Nephrol. 2004 Mar;15(3):722-32. doi: 10.1097/01.asn.0000113552.59155.72. J Am Soc Nephrol. 2004. PMID: 14978175 Free article.
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. Weber S, et al. Kidney Int. 2004 Aug;66(2):571-9. doi: 10.1111/j.1523-1755.2004.00776.x. Kidney Int. 2004. PMID: 15253708 Free article.
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. Frishberg Y, et al. J Am Soc Nephrol. 2002 Feb;13(2):400-5. J Am Soc Nephrol. 2002. PMID: 11805168 Free article.
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; FSGS Spanish Study Group. Santín S, et al. Clin J Am Soc Nephrol. 2011 Feb;6(2):344-54. doi: 10.2215/CJN.03770410. Epub 2010 Oct 14. Clin J Am Soc Nephrol. 2011. PMID: 20947785 Free PMC article.
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. Dhandapani MC, et al. Clin Exp Nephrol. 2017 Feb;21(1):127-133. doi: 10.1007/s10157-016-1237-0. Epub 2016 Jan 28. Clin Exp Nephrol. 2017. PMID: 26820844
NPHS2 variation in Chinese southern infants with late steroid-resistant nephrotic syndrome.
Dai Y, Yang H, Gao P, Liu WD. Dai Y, et al. Ren Fail. 2014 Oct;36(9):1395-8. doi: 10.3109/0886022X.2014.947515. Epub 2014 Aug 12. Ren Fail. 2014. PMID: 25112471
Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome.
Chernin G, Heeringa SF, Gbadegesin R, Liu J, Hinkes BG, Vlangos CN, Vega-Warner V, Hildebrandt F. Chernin G, et al. Pediatr Nephrol. 2008 Sep;23(9):1455-60. doi: 10.1007/s00467-008-0861-7. Epub 2008 Jun 10. Pediatr Nephrol. 2008. PMID: 18543005 Free PMC article.
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. Berdeli A, et al. Pediatr Nephrol. 2007 Dec;22(12):2031-40. doi: 10.1007/s00467-007-0595-y. Epub 2007 Sep 25. Pediatr Nephrol. 2007. PMID: 17899208
Genetic mutation in Egyptian children with steroid-resistant nephrotic syndrome.
Thomas MM, Abdel-Hamid MS, Mahfouz NN, Ghobrial EE. Thomas MM, et al. J Formos Med Assoc. 2018 Jan;117(1):48-53. doi: 10.1016/j.jfma.2017.02.012. Epub 2017 Apr 3. J Formos Med Assoc. 2018. PMID: 28385484 Free article.
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. Yu Z, et al. Nephrol Dial Transplant. 2005 May;20(5):902-8. doi: 10.1093/ndt/gfh769. Epub 2005 Mar 15. Nephrol Dial Transplant. 2005. PMID: 15769810
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