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Journal Abstract Search

104 related items for PubMed ID: 5437914

  • 1. Hyperpyruvicemia with hyper-alpha-alaninemia. Report of a case with neuro-ophthalmologic abnormalities.
    Podos SM.
    Arch Ophthalmol; 1970 Apr; 83(4):504-5. PubMed ID: 5437914
    [No Abstract] [Full Text] [Related]

  • 2. [Intermittent ataxia with hyperpyruvicemia and hyperalaninuria (pyruvate decarboxylase deficiency)].
    Guibaud P.
    Pediatrie; 1971 Jun; 26(4):441-4. PubMed ID: 5568955
    [No Abstract] [Full Text] [Related]

  • 3. Abnormally high levels of lactate and pyruvate in cerebrospinal fluid of hyperalaninemia with hyperpyruvicemia.
    Yoshida T, Tada K, Arakawa T.
    Tohoku J Exp Med; 1970 Aug; 101(4):375-8. PubMed ID: 5482833
    [No Abstract] [Full Text] [Related]

  • 4. Ocular manifestations in aminoacidopathies.
    François J.
    Adv Ophthalmol; 1972 Aug; 25():28-103. PubMed ID: 4560371
    [No Abstract] [Full Text] [Related]

  • 5. Intermittent cerebellar ataxia associated with hyperpyruvic acidemia, hyperalaninemia, and hyperalaninuria.
    Lonsdale D, Faulkner WR, Price JW, Smeby RR.
    Pediatrics; 1969 Jun; 43(6):1025-34. PubMed ID: 5786203
    [No Abstract] [Full Text] [Related]

  • 6. Alaninuria, associated with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus in two sisters.
    Stimmler L, Jensen N, Toseland P.
    Arch Dis Child; 1970 Oct; 45(243):682-5. PubMed ID: 5477682
    [Abstract] [Full Text] [Related]

  • 7. Hyperalaninemia with pyruvicemia.
    Lonsdale D.
    N Engl J Med; 1968 May 30; 278(22):1235. PubMed ID: 5647752
    [No Abstract] [Full Text] [Related]

  • 8. [Neuro-ophthalmologic involvement in 2 cases of dyslipidosis].
    Tchicaloff M.
    Rev Otoneuroophtalmol; 1969 Nov 30; 41(7):401. PubMed ID: 5403010
    [No Abstract] [Full Text] [Related]

  • 9. [New etiologic approach to periodic ketoacidosis in children].
    Boisse J.
    Can Med Assoc J; 1971 Aug 07; 105(3):295-300. PubMed ID: 5001373
    [No Abstract] [Full Text] [Related]

  • 10. [Eye manifestations of amino acid disorders].
    Greco GM, Magli A.
    Minerva Pediatr; 1978 May 31; 30(10):761-80. PubMed ID: 353484
    [No Abstract] [Full Text] [Related]

  • 11. Hyper-beta-alaninemia associated with beta-aminoaciduria and gamma-aminobutyricaciduria, somnolence and seizures.
    Scriver CR, Pueschel S, Davies E.
    N Engl J Med; 1966 Mar 24; 274(12):635-43. PubMed ID: 17926374
    [Abstract] [Full Text] [Related]

  • 12. [Inborn errors of metabolism, associated with ocular symptoms].
    Oura T.
    Nihon Ganka Kiyo; 1969 Aug 24; 20(8):749-58. PubMed ID: 5391478
    [No Abstract] [Full Text] [Related]

  • 13. [Ocular complications of congenital metabolism errors].
    Goux JP, Kallay O.
    Bull Soc Belge Ophtalmol; 1971 Aug 24; 157(1):9-322. PubMed ID: 5565533
    [No Abstract] [Full Text] [Related]

  • 14. [Suspected clinical diagnosis of genetic metabolic disorders in prevention and daily practice].
    Grosser V, Knapp A.
    Z Arztl Fortbild (Jena); 1973 Dec 15; 67(24):1233-8. PubMed ID: 4791811
    [No Abstract] [Full Text] [Related]

  • 15. Pyruvic acidemia with hyperalaninemia: vitamin B1 dependency.
    Lonsdale D, Faulkner WR, Price W, Smeby RR.
    J Pediatr; 1969 May 15; 74(5):827-8. PubMed ID: 5778846
    [No Abstract] [Full Text] [Related]

  • 16.
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  • 17. A urea cycle defect presenting as acute cerebellar ataxia in a 3-year-old girl.
    Keller C, Shapira SK, Clark GD.
    J Child Neurol; 1998 Feb 15; 13(2):93-5. PubMed ID: 9512312
    [No Abstract] [Full Text] [Related]

  • 18.
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    [No Abstract] [Full Text] [Related]

  • 19. [Aminoaciduria and ocular pathology].
    Ardouin M, Urvoy M, Turquois JP, Chaneac M.
    Bull Soc Ophtalmol Fr; 1980 Feb 15; 80(4-5):409-12. PubMed ID: 7460175
    [No Abstract] [Full Text] [Related]

  • 20.
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    [No Abstract] [Full Text] [Related]

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