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Journal Abstract Search

661 related items for PubMed ID: 21734084

  • 21. Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in children.
    Vivante A, Chacham OS, Shril S, Schreiber R, Mane SM, Pode-Shakked B, Soliman NA, Koneth I, Schiffer M, Anikster Y, Hildebrandt F.
    Pediatr Nephrol; 2019 Sep; 34(9):1607-1613. PubMed ID: 31001663
    [Abstract] [Full Text] [Related]

  • 22. Genotype-phenotype associations in WT1 glomerulopathy.
    Lipska BS, Ranchin B, Iatropoulos P, Gellermann J, Melk A, Ozaltin F, Caridi G, Seeman T, Tory K, Jankauskiene A, Zurowska A, Szczepanska M, Wasilewska A, Harambat J, Trautmann A, Peco-Antic A, Borzecka H, Moczulska A, Saeed B, Bogdanovic R, Kalyoncu M, Simkova E, Erdogan O, Vrljicak K, Teixeira A, Azocar M, Schaefer F, PodoNet Consortium.
    Kidney Int; 2014 May; 85(5):1169-78. PubMed ID: 24402088
    [Abstract] [Full Text] [Related]

  • 23. 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]

  • 24. Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis.
    Santín S, García-Maset R, Ruíz P, Giménez I, Zamora I, Peña A, Madrid A, Camacho JA, Fraga G, Sánchez-Moreno A, Cobo MA, Bernis C, Ortiz A, de Pablos AL, Pintos G, Justa ML, Hidalgo-Barquero E, Fernández-Llama P, Ballarín J, Ars E, Torra R, FSGS Spanish Study Group.
    Kidney Int; 2009 Dec; 76(12):1268-76. PubMed ID: 19812541
    [Abstract] [Full Text] [Related]

  • 25. Urinary cytokines and steroid responsiveness in idiopathic nephrotic syndrome of childhood.
    Woroniecki RP, Shatat IF, Supe K, Du Z, Kaskel FJ.
    Am J Nephrol; 2008 Dec; 28(1):83-90. PubMed ID: 17914249
    [Abstract] [Full Text] [Related]

  • 26. Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome.
    Santín S, Bullich G, Tazón-Vega B, García-Maset R, Giménez I, Silva I, Ruíz P, Ballarín J, Torra R, Ars E.
    Clin J Am Soc Nephrol; 2011 May; 6(5):1139-48. PubMed ID: 21415313
    [Abstract] [Full Text] [Related]

  • 27. Multi-drug resistance-1 gene polymorphisms in nephrotic syndrome: impact on susceptibility and response to steroids.
    Youssef DM, Attia TA, El-Shal AS, Abduelometty FA.
    Gene; 2013 Nov 10; 530(2):201-7. PubMed ID: 23994685
    [Abstract] [Full Text] [Related]

  • 28. A novel TRPC6 mutation that causes childhood FSGS.
    Heeringa SF, Möller CC, Du J, Yue L, Hinkes B, Chernin G, Vlangos CN, Hoyer PF, Reiser J, Hildebrandt F.
    PLoS One; 2009 Nov 10; 4(11):e7771. PubMed ID: 19936226
    [Abstract] [Full Text] [Related]

  • 29. 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]

  • 30. Functional analysis of promoter mutations in the ACTN4 and SYNPO genes in focal segmental glomerulosclerosis.
    Dai S, Wang Z, Pan X, Wang W, Chen X, Ren H, Hao C, Han B, Chen N.
    Nephrol Dial Transplant; 2010 Mar 10; 25(3):824-35. PubMed ID: 19666657
    [Abstract] [Full Text] [Related]

  • 31. [Four cases of nephrotic syndrome with TRPC6 gene variations and literature review].
    Sun LW, Sun L, Wang P, Kang YL, Wu Y, Zhu GH, Huang WY.
    Zhonghua Er Ke Za Zhi; 2021 Mar 02; 59(3):223-227. PubMed ID: 33657698
    [Abstract] [Full Text] [Related]

  • 32. TRPC6 and FSGS: the latest TRP channelopathy.
    Mukerji N, Damodaran TV, Winn MP.
    Biochim Biophys Acta; 2007 Aug 02; 1772(8):859-68. PubMed ID: 17459670
    [Abstract] [Full Text] [Related]

  • 33. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 02; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 34. Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome.
    Büscher AK, Kranz B, Büscher R, Hildebrandt F, Dworniczak B, Pennekamp P, Kuwertz-Bröking E, Wingen AM, John U, Kemper M, Monnens L, Hoyer PF, Weber S, Konrad M.
    Clin J Am Soc Nephrol; 2010 Nov 02; 5(11):2075-84. PubMed ID: 20798252
    [Abstract] [Full Text] [Related]

  • 35. [A novel mutation of NPHS2 identified in a Chinese family with steroid-resistant nephrotic syndrome].
    Yu ZH, Ding J, Guan N, Shi Y, Zhang JJ, Huang JP, Yao Y, Yang JY.
    Zhonghua Er Ke Za Zhi; 2004 Feb 02; 42(2):108-12. PubMed ID: 15059485
    [Abstract] [Full Text] [Related]

  • 36. Novel gain-of-function mutation of TRPC6 Q134P contributes to late onset focal segmental glomerulosclerosis in a Chinese pedigree.
    Liu Z, Zhang H, Zhao S, Zhang Q, Zhang R, Han Y, Shao L, Zhao X.
    Nephrology (Carlton); 2021 Dec 02; 26(12):1018-1025. PubMed ID: 34387384
    [Abstract] [Full Text] [Related]

  • 37. NPHS2 mutations in adult patients with primary focal segmental glomerulosclerosis.
    Monteiro EJ, Pereira AC, Pereira AB, Krieger JE, Mastroianni-Kirsztajn G.
    J Nephrol; 2006 Dec 02; 19(3):366-71. PubMed ID: 16874699
    [Abstract] [Full Text] [Related]

  • 38. 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 02; 17(1):227-31. PubMed ID: 16291839
    [Abstract] [Full Text] [Related]

  • 39. Pattern of steroid resistant nephrotic syndrome in children living in the kingdom of Saudi Arabia: a single center study.
    Kari JA, Halawani M, Mokhtar G, Jalalah SM, Anshasi W.
    Saudi J Kidney Dis Transpl; 2009 Sep 02; 20(5):854-7. PubMed ID: 19736491
    [Abstract] [Full Text] [Related]

  • 40. Molecular basis of steroid-resistant nephrotic syndrome.
    Antignac C.
    Nefrologia; 2005 Sep 02; 25 Suppl 2():25-8. PubMed ID: 16050398
    [Abstract] [Full Text] [Related]

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