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Journal Abstract Search

142 related items for PubMed ID: 804362

  • 1. The significance of variation in the selectivity of proteinuria.
    White RH, Mills RJ, Beetham R, Raine DN.
    Clin Nephrol; 1975 Feb; 3(2):42-7. PubMed ID: 804362
    [Abstract] [Full Text] [Related]

  • 2. [Tubular involvement in glomerular diseases of the kidney (author's transl)].
    Lubee G, Balzar E.
    Wien Klin Wochenschr; 1977 Jan 21; 89(2):62-4. PubMed ID: 320767
    [Abstract] [Full Text] [Related]

  • 3. [Synoptic pathology of glomerular diseases in childhood].
    Thoenes W.
    Monatsschr Kinderheilkd; 1983 Jun 21; 131(6):343-50. PubMed ID: 6888389
    [No Abstract] [Full Text] [Related]

  • 4. Selectivity of proteinuria: an evaluation of the immunochemical and gel filtration techniques.
    Pesce AJ, Gaizutis M, Pollak VE.
    J Lab Clin Med; 1970 Apr 21; 75(4):586-606. PubMed ID: 4986371
    [No Abstract] [Full Text] [Related]

  • 5. Electrophoresis patterns of proteinuria in various renal diseases of childhood.
    Zajaczkowska M, Borzecka H, Zinkiewicz Z, Biaduń U.
    Ann Univ Mariae Curie Sklodowska Med; 2003 Apr 21; 58(1):362-6. PubMed ID: 15315016
    [Abstract] [Full Text] [Related]

  • 6. The prognosis of idiopathic nephrotic syndrome: a comparative study between the index of selectivity of proteinuria and the findings in renal biopsies.
    Schwarz R, Rossipal E.
    Padiatr Padol; 1980 Apr 21; 15(2):131-6. PubMed ID: 7432805
    [Abstract] [Full Text] [Related]

  • 7. [Terminal complement complex (TCC) levels in urine in patients with renal diseases].
    Yasuda K.
    Hokkaido Igaku Zasshi; 2001 Mar 21; 76(2):71-84. PubMed ID: 11344904
    [Abstract] [Full Text] [Related]

  • 8. [Haematuria in children. I. Differential diagnosis of haematuria in childhood (author's transl)].
    Mehls O, Schärer K, Michalk D.
    Monatsschr Kinderheilkd (1902); 1978 Feb 21; 126(2):53-6. PubMed ID: 634289
    [Abstract] [Full Text] [Related]

  • 9. Characteristic ultrastructural lesion of the glomerular basement membrane in progressive hereditary nephritis (Alport's syndrome).
    Hinglais N, Grünfeld JP, Bois E.
    Lab Invest; 1972 Nov 21; 27(5):473-87. PubMed ID: 4653971
    [No Abstract] [Full Text] [Related]

  • 10. Urinary excretion of hydroxylysine and its glycosides in Alport's syndrome and several other glomerulopathies.
    Schröder CH, Monnens LA, van Lith-Zanders HM, Trijbels JM, Veerkamp JH, Langeveld JP.
    Nephron; 1986 Nov 21; 44(2):103-7. PubMed ID: 3774073
    [Abstract] [Full Text] [Related]

  • 11. Familial glomerular disease with asymptomatic proteinuria and nephrotic syndrome: a new clinical entity.
    Mathis BJ, Calabrese KE, Slick GL.
    J Am Osteopath Assoc; 1992 Jul 21; 92(7):875-80, 883-4. PubMed ID: 1429048
    [Abstract] [Full Text] [Related]

  • 12. [Demonstration of mesangial IgA deposits in kidney biopsies of pediatric patients: comparison with the clinical picture].
    Kern BE, di Rocco D, Lütschg J, Lüthy C, Zimmermann A, Gerber HA, Oetliker OH, Bianchetti MG.
    Praxis (Bern 1994); 1995 Oct 10; 84(41):1158-64. PubMed ID: 7481326
    [Abstract] [Full Text] [Related]

  • 13. Hereditary glomerulonephritis of non-Alport type.
    Doherty CC, Middleton DT, Hill CM.
    Proc Eur Dial Transplant Assoc; 1983 Oct 10; 19():575-81. PubMed ID: 6878256
    [Abstract] [Full Text] [Related]

  • 14. [Disordered permeability of the glomerular filter for middle- and high-molecular serum proteins in various morphologic types and stages of chronic glomerulonephritis].
    Ratner MIa, Fedorova ND.
    Ter Arkh; 1988 Oct 10; 60(11):112-6. PubMed ID: 3238561
    [Abstract] [Full Text] [Related]

  • 15. Quantitation of proteinuria by use of single random spot urine collection.
    Chahar OP, Bundella B, Chahar CK, Purohit M.
    J Indian Med Assoc; 1993 Apr 10; 91(4):86-7. PubMed ID: 8409488
    [Abstract] [Full Text] [Related]

  • 16. Focal segmental glomerulosclerosis, crescent, and rapidly progressive renal failure.
    Ramirez F, Travis LB, Cunningham RJ, Cavallo T, Rajarman S, Brouhard BH, Ellis EN.
    Int J Pediatr Nephrol; 1982 Sep 10; 3(3):175-8. PubMed ID: 7141789
    [Abstract] [Full Text] [Related]

  • 17. Nephrotic syndrome in African children: lack of evidence for 'tropical nephrotic syndrome'?
    Doe JY, Funk M, Mengel M, Doehring E, Ehrich JH.
    Nephrol Dial Transplant; 2006 Mar 10; 21(3):672-6. PubMed ID: 16326742
    [Abstract] [Full Text] [Related]

  • 18. Proteinuria in children with sickle cell disease.
    Marsenic O, Couloures KG, Wiley JM.
    Nephrol Dial Transplant; 2008 Feb 10; 23(2):715-20. PubMed ID: 18065783
    [Abstract] [Full Text] [Related]

  • 19. IgG-associated primary glomerulonephritis in children.
    Yoshikawa N, Iijima K, Shimomura M, Nakamura H, Ito H.
    Clin Nephrol; 1994 Nov 10; 42(5):281-7. PubMed ID: 7851027
    [Abstract] [Full Text] [Related]

  • 20. The significance of focal segmental glomerulosclerosis in oligomeganephronia.
    McGraw M, Poucell S, Sweet J, Baumal R.
    Int J Pediatr Nephrol; 1984 Jun 10; 5(2):67-72. PubMed ID: 6490319
    [Abstract] [Full Text] [Related]

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