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Journal Abstract Search

317 related items for PubMed ID: 12042895

  • 21. [Heterozygotic mutation in NPHS2 gene as a cause of familial steroid resistant nephrotic syndrome in two siblings--case report].
    Drozdz D, Pietrzyk JA, Wierzchowska-Słowiaczek E, Sancewicz-Pach K, Antignac C, Miezyński W.
    Przegl Lek; 2006; 63 Suppl 3():85-6. PubMed ID: 16898497
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  • 24. Thin basement membranes syndrome: a rare cause of erythrocyturia.
    Salwa-Zurawska W, Bortkiewicz E, Turczuk-Bierła I, Maciejewski J.
    Patol Pol; 1992; 43(2):43-4. PubMed ID: 1296174
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  • 25. Immunotactoid glomerulopathy--an unusual deposition disease: report of the first Malaysian case.
    Cheah PL, Looi LM, Ghazalli R, Chua CT.
    Malays J Pathol; 1999 Jun; 21(1):59-62. PubMed ID: 10879280
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  • 26. Clinicopathologic correlations in 100 children with the nephrotic syndrome.
    Srivastava RN, Mayekar G, Chandra RK, Ghai OP.
    Indian Pediatr; 1973 May; 10(5):287-97. PubMed ID: 4760069
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  • 28. Two cases of congenital nephrotic syndrome.
    Iitaka K, Motoyama O, Hojo M, Iwanami N, Koshino H, Nakamura S, Moriya S.
    Clin Exp Nephrol; 2004 Jun; 8(2):146-9. PubMed ID: 15235932
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  • 29. The Czech registry of renal biopsies. Occurrence of renal diseases in the years 1994-2000.
    Rychlík I, Jancová E, Tesar V, Kolsky A, Lácha J, Stejskal J, Stejskalová A, Dusek J, Herout V.
    Nephrol Dial Transplant; 2004 Dec; 19(12):3040-9. PubMed ID: 15507479
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  • 31. Steroid-sensitive nephrotic syndrome associated with positive C1q immunofluorescence.
    Hashimoto S, Ogawa Y, Ishida T, Mochizuki T, Koike T, Sato H, Ueda T.
    Clin Exp Nephrol; 2004 Sep; 8(3):266-9. PubMed ID: 15480906
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  • 33. A case of familial glomerulopathy with fibronectin deposits caused by the Y973C mutation in fibronectin.
    Ertoy Baydar D, Kutlugun AA, Bresin E, Piras R.
    Am J Kidney Dis; 2013 Mar; 61(3):514-8. PubMed ID: 23219110
    [Abstract] [Full Text] [Related]

  • 34. Nail-patella syndrome.
    Sabnis SG, Antonovych TT, Argy WP, Rakowski TA, Gandy DR, Salcedo JR.
    Clin Nephrol; 1980 Sep; 14(3):148-53. PubMed ID: 7418282
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  • 35. Asymptomatic isolated microscopic haematuria: long-term follow-up.
    Chow KM, Kwan BC, Li PK, Szeto CC.
    QJM; 2004 Nov; 97(11):739-45. PubMed ID: 15496530
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  • 36. Macrohematuria with electron-dense deposits in a 14-year-old boy with minimal change nephrotic syndrome.
    Filler G, Robb I, Carpenter B.
    Pediatr Nephrol; 2001 Jan; 16(1):91-3; discussion 94-6. PubMed ID: 11198614
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  • 37. [Isolated permanent proteinuria. 2. Developmental stability. 3. Nosologic significance].
    Antoine B, Symvouldis A, Dardenne M, De Montera H, Bach JF.
    Presse Med (1893); 1969 Jan 11; 77(2):51-3. PubMed ID: 4182077
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  • 38. Spectrum of acute renal failure in nephrotic syndrome with minimal (or minor) glomerular lesions. Role of hemodynamic factors.
    Esparza AR, Kahn SI, Garella S, Abuelo JG.
    Lab Invest; 1981 Dec 11; 45(6):510-21. PubMed ID: 7321524
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  • 39. Glomerular podocytopathy in patients with systemic lupus erythematosus.
    Kraft SW, Schwartz MM, Korbet SM, Lewis EJ.
    J Am Soc Nephrol; 2005 Jan 11; 16(1):175-9. PubMed ID: 15548564
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  • 40. [Renal histological lesions in patients with type II diabetes mellitus].
    Castellano I, Covarsí A, Novillo R, Gómez-Martino JR, Ferrando L.
    Nefrologia; 2002 Jan 11; 22(2):162-9. PubMed ID: 12085417
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