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Journal Abstract Search

145 related items for PubMed ID: 1196703

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  • 5. Four-hydroxyphenylpyruvic acid oxidase deficiency with normal fumarylacetoacetase: a new variant form of hereditary hypertyrosinemia.
    Endo F, Kitano A, Uehara I, Nagata N, Matsuda I, Shinka T, Kuhara T, Matsumoto I.
    Pediatr Res; 1983 Feb; 17(2):92-6. PubMed ID: 6828337
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  • 6. Urinary phenolic acids in tyrosinemia. Identification and quantitation by gas chromatography-mass spectrometry.
    Crawhall JC, Mamer O, Tjoa S, Claveau JC.
    Clin Chim Acta; 1971 Aug; 34(1):47-54. PubMed ID: 5118727
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  • 8. Tyrosyluria in marasmus.
    Dhatt PS, Saini AS, Gupta I, Mehta HC, Singh H.
    Br J Nutr; 1979 Nov; 42(3):387-90. PubMed ID: 116674
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  • 9. An exceptional case of tyrosinosis.
    Wadman SK, van Sprang FJ, Maas JW, Ketting D.
    J Ment Defic Res; 1968 Dec; 12(4):269-81. PubMed ID: 5729527
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  • 11. [Simple method for study of tyrosyluria].
    Humbel R.
    Pharm Acta Helv; 1968 Jan; 43(1):57-64. PubMed ID: 5719458
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  • 16. Aromatic acid excretion in classical phenylketonuria and hyperphenylalaninemic variants.
    Koepp P, Hoffmann B.
    Helv Paediatr Acta; 1974 Nov; 29(5):489-98. PubMed ID: 4452644
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  • 20. Promising new treatment for type I tyrosinemia.
    Heubi JE.
    J Pediatr Gastroenterol Nutr; 1993 Oct; 17(3):340-1. PubMed ID: 8271141
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