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Journal Abstract Search

205 related items for PubMed ID: 18543005

  • 1. 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.
    Pediatr Nephrol; 2008 Sep; 23(9):1455-60. PubMed ID: 18543005
    [Abstract] [Full Text] [Related]

  • 2. Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa.
    Nandlal L, Winkler CA, Bhimma R, Cho S, Nelson GW, Haripershad S, Naicker T.
    Eur J Pediatr; 2022 Oct; 181(10):3595-3606. PubMed ID: 35920919
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. 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; 15(3):722-32. PubMed ID: 14978175
    [Abstract] [Full Text] [Related]

  • 6. Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis - a single-centre experience.
    Bińczak-Kuleta A, Rubik J, Litwin M, Ryder M, Lewandowska K, Taryma-Leśniak O, Clark JS, Grenda R, Ciechanowicz A.
    Bosn J Basic Med Sci; 2014 May; 14(2):89-93. PubMed ID: 24856380
    [Abstract] [Full Text] [Related]

  • 7. Steroid-resistant nephrotic syndrome: impact of genetic testing.
    Kari JA, El-Desoky SM, Gari M, Malik K, Vega-Warner V, Lovric S, Bockenhauer D.
    Ann Saudi Med; 2013 May; 33(6):533-8. PubMed ID: 24413855
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. Eye involvement in children with primary focal segmental glomerulosclerosis.
    Ozaltin F, Heeringa S, Poyraz CE, Bilginer Y, Kadayifcilar S, Besbas N, Topaloglu R, Ozen S, Hildebrandt F, Bakkaloglu A.
    Pediatr Nephrol; 2008 Mar; 23(3):421-7. PubMed ID: 18058136
    [Abstract] [Full Text] [Related]

  • 11. WT1 and NPHS2 mutations in Korean children with steroid-resistant nephrotic syndrome.
    Cho HY, Lee JH, Choi HJ, Lee BH, Ha IS, Choi Y, Cheong HI.
    Pediatr Nephrol; 2008 Jan; 23(1):63-70. PubMed ID: 17934764
    [Abstract] [Full Text] [Related]

  • 12. 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.
    Clin J Am Soc Nephrol; 2011 Feb; 6(2):344-54. PubMed ID: 20947785
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. [NPHS2 Mutation analysis study in children with steroid-resistant nephrotic syndrome].
    Azocar M, Vega Á, Farfán M, Cano F.
    Rev Chil Pediatr; 2016 Sep; 87(1):31-6. PubMed ID: 26455708
    [Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. 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, German Pediatric Nephrology Association (GPN).
    Clin J Am Soc Nephrol; 2016 Feb 05; 11(2):245-53. PubMed ID: 26668027
    [Abstract] [Full Text] [Related]

  • 19. 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 Feb 05; 31(1):144-149. PubMed ID: 32129207
    [Abstract] [Full Text] [Related]

  • 20. 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 05; 21(4):677-684. PubMed ID: 27573339
    [Abstract] [Full Text] [Related]

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