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Journal Abstract Search

323 related items for PubMed ID: 19145239

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
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  • 3. [NPHS2 Mutation analysis study in children with steroid-resistant nephrotic syndrome].
    Azocar M, Vega Á, Farfán M, Cano F.
    Rev Chil Pediatr; 2016 Feb; 87(1):31-6. PubMed ID: 26455708
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  • 4. 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]

  • 5. R229Q polymorphism of NPHS2 gene in patients with late-onset steroid-resistance nephrotic syndrome: a preliminary study.
    Fotouhi N, Ardalan M, Jabbarpour Bonyadi M, Abdolmohammadi R, Kamalifar A, Nasri H, Einollahi B.
    Iran J Kidney Dis; 2013 Sep 10; 7(5):399-403. PubMed ID: 24072153
    [Abstract] [Full Text] [Related]

  • 6. 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 10; 21(4):677-684. PubMed ID: 27573339
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  • 7. 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]

  • 8. 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 10; 28(5):751-7. PubMed ID: 23242530
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  • 10. [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 May 10; 63 Suppl 3():85-6. PubMed ID: 16898497
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  • 12. 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 10; 13(2):249-56. PubMed ID: 19371226
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Genetic screening in adolescents with steroid-resistant nephrotic syndrome.
    Lipska BS, Iatropoulos P, Maranta R, Caridi G, Ozaltin F, Anarat A, Balat A, Gellermann J, Trautmann A, Erdogan O, Saeed B, Emre S, Bogdanovic R, Azocar M, Balasz-Chmielewska I, Benetti E, Caliskan S, Mir S, Melk A, Ertan P, Baskin E, Jardim H, Davitaia T, Wasilewska A, Drozdz D, Szczepanska M, Jankauskiene A, Higuita LM, Ardissino G, Ozkaya O, Kuzma-Mroczkowska E, Soylemezoglu O, Ranchin B, Medynska A, Tkaczyk M, Peco-Antic A, Akil I, Jarmolinski T, Firszt-Adamczyk A, Dusek J, Simonetti GD, Gok F, Gheissari A, Emma F, Krmar RT, Fischbach M, Printza N, Simkova E, Mele C, Ghiggeri GM, Schaefer F, PodoNet Consortium.
    Kidney Int; 2013 Jul 10; 84(1):206-13. PubMed ID: 23515051
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  • 16. 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]

  • 17. 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 10; 14(5):1278-86. PubMed ID: 12707396
    [Abstract] [Full Text] [Related]

  • 18. NPHS2 R229Q polymorphism in steroid resistant nephrotic syndrome: is it responsive to immunosuppressive therapy?
    Mishra OP, Kakani N, Singh AK, Narayan G, Abhinay A, Prasad R, Batra VV.
    J Trop Pediatr; 2014 Jun 10; 60(3):231-7. PubMed ID: 24519673
    [Abstract] [Full Text] [Related]

  • 19. Specific podocin mutations determine age of onset of nephrotic syndrome all the way into adult life.
    Hildebrandt F, Heeringa SF.
    Kidney Int; 2009 Apr 10; 75(7):669-71. PubMed ID: 19282856
    [Abstract] [Full Text] [Related]

  • 20. 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 10; 181(10):3595-3606. PubMed ID: 35920919
    [Abstract] [Full Text] [Related]

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