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Journal Abstract Search

565 related items for PubMed ID: 24402088

  • 1. 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]

  • 2. Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort.
    Trautmann A, Bodria M, Ozaltin F, Gheisari A, Melk A, Azocar M, Anarat A, Caliskan S, Emma F, Gellermann J, Oh J, Baskin E, Ksiazek J, Remuzzi G, Erdogan O, Akman S, Dusek J, Davitaia T, Özkaya O, Papachristou F, Firszt-Adamczyk A, Urasinski T, Testa S, Krmar RT, Hyla-Klekot L, Pasini A, Özcakar ZB, Sallay P, Cakar N, Galanti M, Terzic J, Aoun B, Caldas Afonso A, Szymanik-Grzelak H, Lipska BS, Schnaidt S, Schaefer F, PodoNet Consortium.
    Clin J Am Soc Nephrol; 2015 Apr 07; 10(4):592-600. PubMed ID: 25635037
    [Abstract] [Full Text] [Related]

  • 3. Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome.
    Ruf RG, Schultheiss M, Lichtenberger A, Karle SM, Zalewski I, Mucha B, Everding AS, Neuhaus T, Patzer L, Plank C, Haas JP, Ozaltin F, Imm A, Fuchshuber A, Bakkaloglu A, Hildebrandt F, APN Study Group.
    Kidney Int; 2004 Aug 07; 66(2):564-70. PubMed ID: 15253707
    [Abstract] [Full Text] [Related]

  • 4. Early diagnosis of WT1 nephropathy and follow up in a Chinese multicenter cohort.
    Sun S, Xu L, Bi Y, Wang J, Zhang Z, Tang X, Cao Q, Zhai Y, Chen J, Fang X, Liu J, Fang Y, Xiang T, Qian Y, Wu B, Wang H, Zhou W, Shen J, Dong K, Liu X, Zheng B, Zhang A, Wang X, Wu Y, Ma D, Shen Q, Rao J, Xu H.
    Eur J Med Genet; 2020 Nov 07; 63(11):104047. PubMed ID: 32891756
    [Abstract] [Full Text] [Related]

  • 5. Genotype-phenotype analysis of pediatric patients with WT1 glomerulopathy.
    Ahn YH, Park EJ, Kang HG, Kim SH, Cho HY, Shin JI, Lee JH, Park YS, Kim KS, Ha IS, Cheong HI.
    Pediatr Nephrol; 2017 Jan 07; 32(1):81-89. PubMed ID: 27300205
    [Abstract] [Full Text] [Related]

  • 6. WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis.
    Denamur E, Bocquet N, Baudouin V, Da Silva F, Veitia R, Peuchmaur M, Elion J, Gubler MC, Fellous M, Niaudet P, Loirat C.
    Kidney Int; 2000 May 07; 57(5):1868-72. PubMed ID: 10792605
    [Abstract] [Full Text] [Related]

  • 7. 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 07; 84(1):206-13. PubMed ID: 23515051
    [Abstract] [Full Text] [Related]

  • 8. Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations.
    Schumacher V, Schärer K, Wühl E, Altrogge H, Bonzel KE, Guschmann M, Neuhaus TJ, Pollastro RM, Kuwertz-Bröking E, Bulla M, Tondera AM, Mundel P, Helmchen U, Waldherr R, Weirich A, Royer-Pokora B.
    Kidney Int; 1998 Jun 07; 53(6):1594-600. PubMed ID: 9607189
    [Abstract] [Full Text] [Related]

  • 9. TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype.
    Gigante M, Caridi G, Montemurno E, Soccio M, d'Apolito M, Cerullo G, Aucella F, Schirinzi A, Emma F, Massella L, Messina G, De Palo T, Ranieri E, Ghiggeri GM, Gesualdo L.
    Clin J Am Soc Nephrol; 2011 Jul 07; 6(7):1626-34. PubMed ID: 21734084
    [Abstract] [Full Text] [Related]

  • 10. 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 07; 119(4):e907-19. PubMed ID: 17371932
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. WT1 mutations in steroid-resistant idiopathic nephrotic syndrome.
    Mishra OP, Singh AK, Abhinay A, Narayan G, Prasad R, Batra VV.
    Saudi J Kidney Dis Transpl; 2016 Mar 05; 27(2):417-8. PubMed ID: 26997404
    [No Abstract] [Full Text] [Related]

  • 13. Clinical characteristics and WT1 genetic analysis of patients with steroid resistant nephrotic syndrome accompanied with genitourinary malformations.
    Li JG, Zhao D, Ding J, Xiao HJ, Guan N, Fan QF, Zhang HW.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Dec 05; 32(6):949-57. PubMed ID: 18182709
    [Abstract] [Full Text] [Related]

  • 14. [Clinical characteristics and WT1 genetic analysis of patients with steroid-resistant nephrotic syndrome accompanied with genitourinary malformations].
    Li JG, Zhao D, Ding J, Xiao HJ, Fan QF, Guan N, Chen Y, Zhang HW.
    Zhonghua Er Ke Za Zhi; 2008 Sep 05; 46(9):692-7. PubMed ID: 19099861
    [Abstract] [Full Text] [Related]

  • 15. Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease management.
    Bierzynska A, McCarthy HJ, Soderquest K, Sen ES, Colby E, Ding WY, Nabhan MM, Kerecuk L, Hegde S, Hughes D, Marks S, Feather S, Jones C, Webb NJ, Ognjanovic M, Christian M, Gilbert RD, Sinha MD, Lord GM, Simpson M, Koziell AB, Welsh GI, Saleem MA.
    Kidney Int; 2017 Apr 05; 91(4):937-947. PubMed ID: 28117080
    [Abstract] [Full Text] [Related]

  • 16. Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations.
    Chernin G, Vega-Warner V, Schoeb DS, Heeringa SF, Ovunc B, Saisawat P, Cleper R, Ozaltin F, Hildebrandt F, Members of the GPN Study Group.
    Clin J Am Soc Nephrol; 2010 Sep 05; 5(9):1655-62. PubMed ID: 20595692
    [Abstract] [Full Text] [Related]

  • 17. Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1.
    Lehnhardt A, Karnatz C, Ahlenstiel-Grunow T, Benz K, Benz MR, Budde K, Büscher AK, Fehr T, Feldkötter M, Graf N, Höcker B, Jungraithmayr T, Klaus G, Koehler B, Konrad M, Kranz B, Montoya CR, Müller D, Neuhaus TJ, Oh J, Pape L, Pohl M, Royer-Pokora B, Querfeld U, Schneppenheim R, Staude H, Spartà G, Timmermann K, Wilkening F, Wygoda S, Bergmann C, Kemper MJ.
    Clin J Am Soc Nephrol; 2015 May 07; 10(5):825-31. PubMed ID: 25818337
    [Abstract] [Full Text] [Related]

  • 18. COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome.
    Ozdemir G, Gulhan B, Atayar E, Saygılı S, Soylemezoglu O, Ozcakar ZB, Eroglu FK, Candan C, Demir BK, Soylu A, Yüksel S, Alpay H, Agbas A, Duzova A, Hayran M, Ozaltin F, Topaloglu R.
    Pediatr Nephrol; 2020 Oct 07; 35(10):1941-1952. PubMed ID: 32394188
    [Abstract] [Full Text] [Related]

  • 19. 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 07; 6(2):344-54. PubMed ID: 20947785
    [Abstract] [Full Text] [Related]

  • 20. Wilms' tumor suppressor gene mutations in girls with sporadic isolated steroid-resistant nephrotic syndrome.
    Yang YH, Zhao F, Feng DN, Wang JJ, Wang CF, Huang J, Nie XJ, Xia GZ, Chen GM, Yu ZH.
    Genet Mol Res; 2013 Dec 04; 12(4):6184-91. PubMed ID: 24338413
    [Abstract] [Full Text] [Related]

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