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Journal Abstract Search

150 related items for PubMed ID: 4365835

  • 1. [The family of a patient with galactokinase-defect 2nd communication (author's transl)].
    Kaloud H, Sitzmann FC, Paltauf F, Mayer R.
    Klin Padiatr; 1974 Jan; 186(1):33-6. PubMed ID: 4365835
    [No Abstract] [Full Text] [Related]

  • 2. [An unusual form of galactose metabolism disorder].
    Rubecz I, Ritecz E, Méhes K, Csordás J.
    Orv Hetil; 1971 Dec 19; 112(51):3051-4. PubMed ID: 5136647
    [No Abstract] [Full Text] [Related]

  • 3. Galactokinase-deficiency cataracts in identical twins.
    Oberman AE, Wilson WA, Frasier SD, Donnell GN, Bergren WR.
    Am J Ophthalmol; 1972 Nov 19; 74(5):887-92. PubMed ID: 4644736
    [No Abstract] [Full Text] [Related]

  • 4. Galactokinase deficiency as a cause of cataracts.
    Beutler E, Matsumoto F, Kuhl W, Krill A, Levy N, Sparkes R, Degnan M.
    N Engl J Med; 1973 Jun 07; 288(23):1203-6. PubMed ID: 4700553
    [No Abstract] [Full Text] [Related]

  • 5. [Partial and transitory erythrocyte galactokinase deficiency in a newborn. Biochemical study].
    Vigneron C, Marchal C, Deifts C, Vidailhet M, Pierson M, Neimann N.
    Arch Fr Pediatr; 1970 May 07; 27(5):523-31. PubMed ID: 5425825
    [No Abstract] [Full Text] [Related]

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  • 13. [Activity of enzymes of galactose metabolism in so-called congenital cataract (author's transl)].
    Kaloud H, Sitzmann FC, Schenker H, Prestele H.
    Dtsch Med Wochenschr; 1975 Apr 18; 100(16):873-6. PubMed ID: 164335
    [Abstract] [Full Text] [Related]

  • 14. Cataracts, galactosuria and hypergalactosemia due to galactokinase deficiency in a child. Studies of a kindred.
    Monteleone JA, Beutler E, Monteleone PL, Utz CL, Casey EC.
    Am J Med; 1971 Mar 18; 50(3):403-7. PubMed ID: 5553957
    [No Abstract] [Full Text] [Related]

  • 15. [Galactokinase deficiency].
    Colin J, Voyer M, Thomas D, Charlas J.
    Ann Pediatr (Paris); 1976 May 02; 23(5):371-7. PubMed ID: 16104211
    [No Abstract] [Full Text] [Related]

  • 16. Galactokinase deficiency in twins: clinical and biochemical studies.
    Olambiwonnu NO, McVie R, Ng WG, Frasier SD, Donnell GN.
    Pediatrics; 1974 Mar 02; 53(3):314-8. PubMed ID: 4360930
    [No Abstract] [Full Text] [Related]

  • 17. [Familial deficiency on alpha-1-antitrypsin].
    Wehinger H, Karitzky D, Witt I.
    Z Kinderheilkd; 1971 Mar 02; 110(2):115-27. PubMed ID: 5580606
    [No Abstract] [Full Text] [Related]

  • 18. [Oxalosis: two family studies in Tunisia (author's transl)].
    Ramadhane MS, Khrouf N, Brauner R, Ben Jilani S, Hamza M, Hamza B.
    Ann Pediatr (Paris); 1982 Feb 02; 29(2):148-51. PubMed ID: 7059122
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  • 19. [Cataract due to galactokinase deficiency in a premature infant].
    Colin J, Voyer M, Thomas D, Schapira F, Satge P.
    Arch Fr Pediatr; 1976 Jan 02; 33(1):77-82. PubMed ID: 185981
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  • 20. [Gene frequencies of both forms of galactosaemia in the western Hungarian province of Vas (author's transl)].
    Sitzmann FC, Istvan L, Teubl I, Kaloud H, Cholnoky P.
    Wien Klin Wochenschr; 1978 Jan 06; 90(1):16-20. PubMed ID: 204112
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