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Journal Abstract Search

151 related items for PubMed ID: 4522587

  • 1. [The histological findings of tubular insufficiency in galactosemia, hereditary fructose intolerance, and oculocerebro-renal syndrome (Lowe-syndrome) (author's transl].
    Roschlau G.
    Zentralbl Allg Pathol; 1973; 117(5):488-96. PubMed ID: 4522587
    [No Abstract] [Full Text] [Related]

  • 2. Lowe's syndrome. Pathological studies of four cases.
    Rutsaert J, Segers-Cadranel A, Potvliege P.
    Pathol Eur; 1972; 7(3):249-62. PubMed ID: 4120987
    [No Abstract] [Full Text] [Related]

  • 3. [Modern trends in inborn errors of metabolism (reports) (author's transl)].
    Bickel H, Molz G.
    Verh Dtsch Ges Pathol; 1971; 55():356-75. PubMed ID: 4130732
    [No Abstract] [Full Text] [Related]

  • 4. [Hereditary fructose intolerance (author's transl)].
    Rossner JA, Feist D.
    Verh Dtsch Ges Pathol; 1971; 55():376-85. PubMed ID: 4130733
    [No Abstract] [Full Text] [Related]

  • 5. [HEREDITARY INTOLERANCE TO FRUCTOSE].
    ROYER P, LESTRADET H, HABIB R, LARDINOIS R, DESBUQUOIS B.
    Bull Mem Soc Med Hop Paris; 1971; 115():805-23. PubMed ID: 14186900
    [No Abstract] [Full Text] [Related]

  • 6. A familial syndrome of growth retardation, severe Fanconi-type renal disease and glomerular changes--a new entity?
    Bartsocas CS, Bernstein J, Orloff S, Chandra R, Schulman JD.
    Int J Pediatr Nephrol; 1986; 7(2):101-6. PubMed ID: 3721723
    [Abstract] [Full Text] [Related]

  • 7. [Hypercalciuria and hereditary fructose intolerance (author's transl)].
    Betend B, Gillet P, David L, François R.
    Arch Fr Pediatr; 1982 Feb; 39(2):99-100. PubMed ID: 7073441
    [Abstract] [Full Text] [Related]

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  • 10. [Renal function disorders in congenital metabolic abnormalities. 2. Renal function disorders in Lowe's and de Toni-Fanconi syndrome].
    Ito K.
    Nihon Shonika Gakkai Zasshi; 1971 Jun; 75(6):464-75. PubMed ID: 5104633
    [No Abstract] [Full Text] [Related]

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  • 12. [Fructose intolerance and related diseases].
    Perheentupa J.
    Duodecim; 1972 Jun; 88(1):97-101. PubMed ID: 4501714
    [No Abstract] [Full Text] [Related]

  • 13. [Hereditary defects of fructose and galactose metabolism].
    Gitzelmann R, Baerlocher K, Prader A.
    Monatsschr Kinderheilkd (1902); 1973 May; 121(5):174-80. PubMed ID: 4351554
    [No Abstract] [Full Text] [Related]

  • 14. [Hepatic histological and ultrastructural aspects of 2 cases of hereditary fructose intolerance].
    Ceccamea A, Nardi F, Faraggiana T, Bonamico M, Giardini O, Cardi E.
    Minerva Pediatr; 1980 Apr 30; 32(8):521-30. PubMed ID: 7393184
    [No Abstract] [Full Text] [Related]

  • 15. [Hereditary fructose intolerance. Early manifestation in newborns and young infants (author's transl)].
    Vieweg B, Posselt HG, Streb H, Strobel S.
    Monatsschr Kinderheilkd; 1982 Jan 30; 130(1):21-6. PubMed ID: 7062914
    [No Abstract] [Full Text] [Related]

  • 16. [Hereditary fructose intolerance (author's transl)].
    Thanner F.
    Monatsschr Kinderheilkd (1902); 1977 Jul 30; 125(7):677-86. PubMed ID: 331087
    [Abstract] [Full Text] [Related]

  • 17. Manifestation of hereditary fructose intolerance.
    Raju L, Chessells JM, Kemball M.
    Br Med J; 1971 May 22; 2(5759):446-7. PubMed ID: 5576008
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  • 19. [Hereditary fructose intolerance: a case report (author's transl)].
    Demi M, Ventura MR, Bonofiglio A.
    Pediatr Med Chir; 1981 May 22; 3(1):55-9. PubMed ID: 7301620
    [No Abstract] [Full Text] [Related]

  • 20. [Liver fructose-1-phosphate and fructose-1,6-diphosphate aldolase deficiency in hereditary fructose intolerance (author's transl)].
    Joosten R, Berzdorf M, de Barsy T, Habedank M.
    Klin Padiatr; 1981 Sep 22; 193(5):392-3. PubMed ID: 7289434
    [No Abstract] [Full Text] [Related]

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