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Journal Abstract Search

235 related items for PubMed ID: 6749416

  • 21. Benign familial hematuria due to mutation of the type IV collagen alpha4 gene.
    Lemmink HH, Nillesen WN, Mochizuki T, Schröder CH, Brunner HG, van Oost BA, Monnens LA, Smeets HJ.
    J Clin Invest; 1996 Sep 01; 98(5):1114-8. PubMed ID: 8787673
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  • 22. Glomerular basement membrane changes in hereditary glomerular diseases.
    Gubler MC, Levy M, Naizot C, Habib R.
    Ren Physiol; 1980 Sep 01; 3(1-6):405-13. PubMed ID: 7323434
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  • 25. The specificity of split renal membranes in hereditary nephritis.
    Kohaut EC, Singer DB, Nevels BK, Hill LL.
    Arch Pathol Lab Med; 1976 Sep 01; 100(9):475-9. PubMed ID: 988990
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  • 26. [Nail-patella syndrome: clinico-pathologic characteristics].
    Trinn C, Szöke B, Magyarlaki T, Turi S, Ormos J, Nagy J.
    Orv Hetil; 1996 Oct 13; 137(41):2253-6. PubMed ID: 8992423
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  • 29. Evolution of glomerular basement membrane lesions in a male patient with Alport syndrome: ultrastructural and morphometric study.
    Cangiotti AM, Sessa A, Meroni M, Montironi R, Ragaiolo M, Mambelli V, Cinti S.
    Nephrol Dial Transplant; 1996 Sep 13; 11(9):1829-34. PubMed ID: 8918631
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  • 32. Differential diagnosis between X-linked Alport syndrome and thin basement membrane nephropathy.
    Rizzoni G, Massella L.
    Kidney Int; 2004 Sep 13; 66(3):1289-90; author reply 1290. PubMed ID: 15327434
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  • 34. Recurrent hematuria in childhood.
    Singer DB, Hill LL, Rosenberg HS, Marshall J, Swenson R.
    N Engl J Med; 1968 Jul 04; 279(1):7-12. PubMed ID: 5658025
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  • 39. Hereditary nephritis mimicking immune complex-mediated glomerulonephritis.
    Nasr SH, Markowitz GS, Goldstein CS, Fildes RD, D'Agati VD.
    Hum Pathol; 2006 May 04; 37(5):547-54. PubMed ID: 16647952
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