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Journal Abstract Search

193 related items for PubMed ID: 19099861

  • 41. 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; 84(1):206-13. PubMed ID: 23515051
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  • 46. TRPC6 gene variants in Turkish children with steroid-resistant nephrotic syndrome.
    Mir S, Yavascan O, Berdeli A, Sozeri B.
    Nephrol Dial Transplant; 2012 Jan; 27(1):205-9. PubMed ID: 21511817
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  • 48. Isolated steroid-resistant nephrotic syndrome in a Chinese child carrying a de novo mutation in WT1 gene:a case report and literature review.
    Li Y, Tian C, Wang Y, Ma G, Chen R.
    BMC Pediatr; 2022 Jun 16; 22(1):349. PubMed ID: 35710404
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  • 49. Steroid Resistant Nephrotic Syndrome-Genetic Consideration.
    Tasic V, Gucev Z, Polenakovic M.
    Pril (Makedon Akad Nauk Umet Odd Med Nauki); 2015 Jun 16; 36(3):5-12. PubMed ID: 27442391
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  • 50. Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms.
    Klamt B, Koziell A, Poulat F, Wieacker P, Scambler P, Berta P, Gessler M.
    Hum Mol Genet; 1998 Apr 16; 7(4):709-14. PubMed ID: 9499425
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  • 55. 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 16; 27(2):417-8. PubMed ID: 26997404
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  • 56. Cyclosporine in patients with steroid-resistant nephrotic syndrome: an open-label, nonrandomized, retrospective study.
    Ghiggeri GM, Catarsi P, Scolari F, Caridi G, Bertelli R, Carrea A, Sanna-Cherchi S, Emma F, Allegri L, Cancarini G, Rizzoni GF, Perfumo F.
    Clin Ther; 2004 Sep 16; 26(9):1411-8. PubMed ID: 15531003
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  • 57. A girl with MIRAGE syndrome who developed steroid-resistant nephrotic syndrome: a case report.
    Ishiwa S, Kamei K, Tanase-Nakao K, Shibata S, Matsunami K, Takeuchi I, Sato M, Ishikura K, Narumi S.
    BMC Nephrol; 2020 Aug 12; 21(1):340. PubMed ID: 32787808
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  • 58. Successful treatment of steroid-resistant nephrotic syndrome associated with WT1 mutations.
    Gellermann J, Stefanidis CJ, Mitsioni A, Querfeld U.
    Pediatr Nephrol; 2010 Jul 12; 25(7):1285-9. PubMed ID: 20191369
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  • 59. Intrauterine growth restriction leads to a dysregulation of Wilms' tumour supressor gene 1 (WT1) and to early podocyte alterations.
    Menendez-Castro C, Hilgers KF, Amann K, Daniel C, Cordasic N, Wachtveitl R, Fahlbusch F, Plank C, Dötsch J, Rascher W, Hartner A.
    Nephrol Dial Transplant; 2013 Jun 12; 28(6):1407-17. PubMed ID: 23229934
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