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Journal Abstract Search

135 related items for PubMed ID: 17109732

  • 21. In vivo expression of podocyte slit diaphragm-associated proteins in nephrotic patients with NPHS2 mutation.
    Zhang SY, Marlier A, Gribouval O, Gilbert T, Heidet L, Antignac C, Gubler MC.
    Kidney Int; 2004 Sep; 66(3):945-54. PubMed ID: 15327385
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  • 22. 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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  • 23. CD80, suPAR and nephrotic syndrome in a case of NPHS2 mutation.
    Cara-Fuentes G, Araya C, Wei C, Rivard C, Ishimoto T, Reiser J, Johnson RJ, Garin EH.
    Nefrologia; 2013 Aug 28; 33(5):727-31. PubMed ID: 24089165
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  • 24. 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 28; 18(5):412-6. PubMed ID: 12687458
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  • 25. Mutated podocin manifesting as CMV-associated congenital nephrotic syndrome.
    Frishberg Y, Rinat C, Feinstein S, Becker-Cohen R, Megged O, Schlesinger Y.
    Pediatr Nephrol; 2003 Mar 28; 18(3):273-5. PubMed ID: 12644922
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  • 26. NPHS2 gene mutations in azerbaijani children with steroid-resistant nephrotic syndrome.
    Baylarov R, Senol O, Atan M, Berdeli A.
    Saudi J Kidney Dis Transpl; 2020 Mar 28; 31(1):144-149. PubMed ID: 32129207
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  • 28. Clinical features and mutational survey of NPHS2 (podocin) in Japanese children with focal segmental glomerulosclerosis who underwent renal transplantation.
    Furue T, Hattori M, Tsukaguchi H, Kitamura A, Oomori T, Ogino D, Nakakura H, Ashida A, Miura K, Hisano M, Takahashi K, Chikamoto H, Akioka Y, Sakano T.
    Pediatr Transplant; 2008 May 28; 12(3):341-6. PubMed ID: 18208440
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  • 30. NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review.
    Franceschini N, North KE, Kopp JB, McKenzie L, Winkler C.
    Genet Med; 2006 Feb 28; 8(2):63-75. PubMed ID: 16481888
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  • 34. Congenital nephrotic syndrome and recurrence of proteinuria after renal transplantation.
    Holmberg C, Jalanko H.
    Pediatr Nephrol; 2014 Dec 28; 29(12):2309-17. PubMed ID: 24682440
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  • 35. NPHS2 (Podocin) mutations in nephrotic syndrome. Clinical spectrum and fine mechanisms.
    Caridi G, Perfumo F, Ghiggeri GM.
    Pediatr Res; 2005 May 28; 57(5 Pt 2):54R-61R. PubMed ID: 15817495
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