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Journal Abstract Search

125 related items for PubMed ID: 5859057

  • 1. [Electrophoretic analysis of proteinurias encountered in the course of renal tubular disorders].
    Traeger J, François R, Creyssel R, Revillard JP, Manuel Y, Freycon MT, Site M.
    J Urol Nephrol (Paris); 1965 Sep; 71(9):728-35. PubMed ID: 5859057
    [No Abstract] [Full Text] [Related]

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  • 3. [Value of systematic association of "renal puncture-biopsy and electrophoresis of urinary proteins" in the study of kidney diseases and proteinuria in childhood].
    Gaillard L, Salle B, Manuel Y, Delphin D.
    Ann Pediatr (Paris); 1969 Oct 02; 16(10):615-23. PubMed ID: 5357399
    [No Abstract] [Full Text] [Related]

  • 4. [Determination of the concentration of amino-nitrates as a supplementary analysis in the examination of kidney function].
    Dovat VN, Obradović D, Stanković J.
    Med Pregl; 1971 Oct 02; 24(8):373-5. PubMed ID: 5135671
    [No Abstract] [Full Text] [Related]

  • 5. [An electrophoretic study of urinary proteins in kidney diseases].
    Peleshchuk AP, Mel'man NIa, Krimkevich EI.
    Vrach Delo; 1968 Apr 02; 4():22-5. PubMed ID: 5664599
    [No Abstract] [Full Text] [Related]

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  • 9. Ocular manifestations of hereditary renal disorders.
    Giangiacomo J.
    Pediatr Ann; 1977 Jan 02; 6(1):126-9. PubMed ID: 401982
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  • 10.
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  • 11. [Familial proteinuria of the tubular type with appearance of the Bartter syndrome in 1 of the members of the family: a new disease?].
    François R, Bertrand J, Pellet, Salle B, Moreau P, Manuel P.
    J Urol Nephrol (Paris); 1967 Jan 02; 73(10):829-39. PubMed ID: 5596279
    [No Abstract] [Full Text] [Related]

  • 12. [Tubular proteinurias].
    Maiorca R, Scarpioni L, Cambi V, Carrara G, Dall'Aglio P.
    Recenti Prog Med; 1968 Feb 02; 44(2):154-77. PubMed ID: 4909756
    [No Abstract] [Full Text] [Related]

  • 13. Evaluation of infants and children for kidney disease.
    Goldsmith DI, Spitzer A.
    Paediatrician; 1979 Feb 02; 8(5-6):246-69. PubMed ID: 392402
    [Abstract] [Full Text] [Related]

  • 14. Sanfilippo disease (mucopolysaccharidosis type III) presenting as transient renal tubular dysfunction.
    Ramaswami U, Van 't Hoff W, Clayton P, Vellodi A.
    J Inherit Metab Dis; 1996 Feb 02; 19(1):87-8. PubMed ID: 8830184
    [No Abstract] [Full Text] [Related]

  • 15. [Contribution of molecular biology to the study of renal tubular diseases].
    Rodríguez Soriano J.
    An Esp Pediatr; 1997 Jun 02; Spec No 1():40-2. PubMed ID: 9382265
    [No Abstract] [Full Text] [Related]

  • 16. Inherited tubular transport disorders.
    Dell KM, Guay-Woodford LM.
    Semin Nephrol; 1999 Jul 02; 19(4):364-73. PubMed ID: 10435674
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  • 17. [Analysis of molecular weight related proteinuria, as a contribution to the diagnosis of renal diseases].
    Boesken WH.
    Med Klin; 1976 Mar 12; 71(11):441-8. PubMed ID: 772389
    [No Abstract] [Full Text] [Related]

  • 18. [Indirect immunoelectrophoresis in the study of urinary proteins].
    Scolozzi R, Careri C, Squerzanti R.
    Minerva Med; 1979 Sep 22; 70(40):2729-33. PubMed ID: 481795
    [Abstract] [Full Text] [Related]

  • 19. [Nephrology].
    Rev Med Brux; 1984 Mar 22; 5(3):159-69. PubMed ID: 6371982
    [No Abstract] [Full Text] [Related]

  • 20. Renal disorders and diseases of the newborn.
    John E.
    Indian J Pediatr; 1985 Mar 22; 52(414):17-42. PubMed ID: 3891610
    [No Abstract] [Full Text] [Related]

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