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Journal Abstract Search

209 related items for PubMed ID: 14217031

  • 1. [MAPLE SYRUP DISEASE WITH FAMILIAL INCIDENCE].
    DIEZEL PB, MARTIN K.
    Virchows Arch Pathol Anat Physiol Klin Med; 1964 May 22; 337():425-45. PubMed ID: 14217031
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  • 7. [Diseases of newborn infants based on inborn anomalies of metabolism. 1. Theoretical principles].
    Plöchl E.
    Wien Med Wochenschr; 1970 Oct 10; 120(41):707-11. PubMed ID: 4918107
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  • 9. MAPLE SYRUP URINE DISEASE; FURTHER OBSERVATIONS.
    WOODY NC, HANCOCK CD.
    Am J Dis Child; 1963 Dec 10; 106():578-85. PubMed ID: 14063708
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  • 13. MAPLE SYRUP URINE DISEASE, WITH PARTICULAR REFERENCE TO DIETOTHERAPY.
    SNYDERMAN SE, NORTON PM, ROITMAN E, HOLT LE.
    Pediatrics; 1964 Oct 10; 34():454-72. PubMed ID: 14212461
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  • 14. Plasma amino acid analyses in two cases of maple syrup urine disease.
    Surarit R, Srisomsap C, Wasant P, Svasti J, Suthatvoravut U, Chokchaichamnankit D, Liammongkolkul S.
    Southeast Asian J Trop Med Public Health; 1999 Oct 10; 30 Suppl 2():138-9. PubMed ID: 11400750
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  • 15. HYPERLYSINEMIA.
    WOODY NC.
    Am J Dis Child; 1964 Nov 10; 108():543-53. PubMed ID: 14209691
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  • 16. [Combined forms of metabolic errors detected in newborn infants].
    Tănase-Mogoş I, Ciortoloman H, Grigorescu G, Popescu M, Ankăr V.
    Physiologie; 1978 Nov 10; 15(4):239-43. PubMed ID: 106407
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  • 17. MAPLE SYRUP URINE DISEASE: A MANIFESTATION OF AN UNUSUAL METABOLIC ERROR.
    DANCIS J.
    Clin Pediatr (Phila); 1964 Jun 10; 3():365-7. PubMed ID: 14154327
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  • 18. [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 10; 46():339-65. PubMed ID: 14122039
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