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Journal Abstract Search

174 related items for PubMed ID: 35935761

  • 21. NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children.
    Maruyama K, Iijima K, Ikeda M, Kitamura A, Tsukaguchi H, Yoshiya K, Hoshii S, Wada N, Uemura O, Satomura K, Honda M, Yoshikawa N.
    Pediatr Nephrol; 2003 May; 18(5):412-6. PubMed ID: 12687458
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  • 25. 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
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  • 27. 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; 66(2):571-9. PubMed ID: 15253708
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  • 29. 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
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  • 31. Molecular Study of Childhood Steroid-Resistant Nephrotic Syndrome: A Hospital-Based Study.
    Singh A, Singh A, Mishra OP, Prasad R, Narayan G, Batra VV, Tabatabaeifar M, Schaefer F.
    J Pediatr Genet; 2022 Sep; 11(3):185-191. PubMed ID: 35990031
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  • 34. Case Report: The Monogenic Familial Steroid-Resistant Nephrotic Syndrome Caused by a Novel Missense Mutation of NPHS2 Gene A593C in a Chinese Family.
    Bai L, Zhuang J, Zhang C, Lu C, Tian X, Jiang H.
    Front Pediatr; 2021 Sep; 9():692727. PubMed ID: 34631609
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  • 38. The podocin mutation R229Q and early recurrence (within the first year) of glomerular disease after renal transplantation.
    Mohey H, Thibaudin L, Laurent B, Berthoux F.
    Ann Transplant; 2013 Aug 28; 18():436-42. PubMed ID: 23982418
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  • 39. Genetic testing in focal segmental glomerulosclerosis: in whom and when?
    Tato AM, Carrera N, García-Murias M, Shabaka A, Ávila A, Mora Mora MT, Rabasco C, Soto K, de la Prada Alvarez FJ, Fernández-Lorente L, Rodríguez-Moreno A, Huerta A, Mon C, García-Carro C, González Cabrera F, Navarro JAM, Romera A, Gutiérrez E, Villacorta J, de Lorenzo A, Avilés B, Garca-González MA, Fernández-Juárez G.
    Clin Kidney J; 2023 Nov 28; 16(11):2011-2022. PubMed ID: 37915894
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