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Journal Abstract Search

494 related items for PubMed ID: 6101930

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  • 3. [Compliance of the diet restricted with leucine, isoleucine and valine in maple syrup urine disease (MSUD) children].
    Kowalik A, Narojek L, Sykut-Cegielska J.
    Rocz Panstw Zakl Hig; 2007; 58(1):95-101. PubMed ID: 17711097
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  • 5. Total branched-chain amino acids requirement in patients with maple syrup urine disease by use of indicator amino acid oxidation with L-[1-13C]phenylalanine.
    Riazi R, Rafii M, Clarke JT, Wykes LJ, Ball RO, Pencharz PB.
    Am J Physiol Endocrinol Metab; 2004 Jul; 287(1):E142-9. PubMed ID: 14970005
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  • 6. [Disorders of leucine, isoleucine and valine metabolism (maple syrup urine disease)].
    Vulović D, Vilhar N, Hajduković R, Marjanović B, Stojanović Lj.
    Srp Arh Celok Lek; 1975 May; 103(5):419-36. PubMed ID: 1188483
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  • 7. American Academy of Pediatrics. Committee on Nutrition: special diets for infants with inborn errors of amino acid metabolism.
    Pediatrics; 1976 May; 57(5):783-92. PubMed ID: 940719
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  • 12. Maple syrup urine disease: branched-chain amino acid concentrations and metabolism in cultured human lymphoblasts.
    Skaper SD, Molden DP, Seegmiller JE.
    Biochem Genet; 1976 Aug; 14(7-8):527-39. PubMed ID: 985377
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  • 15. Enzyme activity in classical and variant forms of maple syrup urine disease.
    Dancis J, Hutzler J, Snyderman SE, Cox RP.
    J Pediatr; 1972 Aug; 81(2):312-20. PubMed ID: 5042489
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  • 18. [Aminoacid metabolism disorders in infancy with special reference to phenylketonuria. II. Aminoacid metabolism and general physiopathology of aminoacidopathies].
    Segni G.
    Minerva Nipiol; 1970 Aug; 20(4):83-110. PubMed ID: 4396023
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  • 20. [CLINICAL, BIOCHEMICAL, AND NEUROPATHOLOGIC ASPECTS OF MAPLE SYRUP URINE DISEASE. A KETOACIDURIA OF THE OPEN CHAIN AMINOACIDS LEUCINE, ISOLEUCINE AND VALINE].
    SILBERMANSCHWARTZMAN J.
    An Fac Med Lima; 1963 Sep; 46():339-65. PubMed ID: 14122039
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