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PUBMED FOR HANDHELDS

Journal Abstract Search


110 related items for PubMed ID: 324700

  • 1. [Some clinical and therapeutic aspects of organico-acidemia and organico-aciduria].
    Piccardo M, Tassara F, Vico L.
    Clin Ter; 1977 Apr 15; 81(1):51-66. PubMed ID: 324700
    [No Abstract] [Full Text] [Related]

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  • 3. [Human fibroblast bank for studying amino acid disorders and organic acidemias].
    del Valle JA, Merinero B, Pérez-Cerdá C, Ugarte M.
    Rev Esp Fisiol; 1982 Apr 15; 38 Suppl():207-10. PubMed ID: 7146578
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  • 4. [Congenital metabolic acidosis in the postnatal period].
    Schreier K, Porath U.
    Dtsch Med Wochenschr; 1978 Jun 02; 103(22):943-7. PubMed ID: 207503
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  • 7. [Hereditary amino acid metabolism disorders. Indications for early diagnosis].
    Kroll S, Zebisch P, Toussaint W.
    Fortschr Med; 1972 Apr 13; 90(11):423-8. PubMed ID: 4680607
    [No Abstract] [Full Text] [Related]

  • 8. Branched-chain organic acidurias.
    Ogier de Baulny H, Saudubray JM.
    Semin Neonatol; 2002 Feb 13; 7(1):65-74. PubMed ID: 12069539
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  • 9. [Primary and secondary hyperaminoaciduria in children (review of the literature)].
    Lebedev VP, Iur'eva EA, Mukhina IuG, Buravina TA, Koroleva IA.
    Vopr Okhr Materin Det; 1970 Nov 13; 15(11):64-8. PubMed ID: 4928437
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  • 11. THE PRIMARY AMINO-ACIDOPATHIES. GENETIC DEFECTS IN THE METABOLISM OF THE AMINO ACIDS.
    DIGEORGE AM, AUERBACH VH.
    Pediatr Clin North Am; 1963 Aug 13; 10():723-44. PubMed ID: 14145016
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  • 13. Plasma amino acid and urine organic acid analyses of methylmalonic acidemia in a Thai infant.
    Srisomsap' C, Wasant P, Svasti J, Chokchaichamnankit D, Liammongkolkul S.
    Southeast Asian J Trop Med Public Health; 1999 Aug 13; 30 Suppl 2():140-2. PubMed ID: 11400752
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  • 14. Liver transplantation: new indications in metabolic disorders?
    Jan D, Poggi F, Laurent J, Rabier D, Jouvet P, Lacaille F, Beringer A, Hubert P, Revillon Y, Saudubray JM.
    Transplant Proc; 1994 Feb 13; 26(1):189-90. PubMed ID: 8108935
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  • 15. A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER.
    EFRON ML, YOUNG D, MOSER HW, MACCREADY RA.
    N Engl J Med; 1964 Jun 25; 270():1378-83. PubMed ID: 14152868
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  • 17. [Propionic acidemia: one case report].
    Yuan L.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1991 Apr 25; 13(2):141-3. PubMed ID: 1831712
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  • 19. Profiles of urinary volatiles from metabolic disorders characterized by unusual odors.
    Burke DG, Halpern B, Malegan D, McCairns E, Danks D, Schlesinger P, Wilken B.
    Clin Chem; 1983 Oct 25; 29(10):1834-8. PubMed ID: 6616835
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  • 20. [Diagnosis of inborn errors of metabolism using tandem mass spectrometry and gas chromatography mass spectrometry].
    Han LS, Ye J, Qiu WJ, Gao XL, Wang Y, Jin J, Gu XF.
    Zhonghua Yi Xue Za Zhi; 2008 Aug 05; 88(30):2122-6. PubMed ID: 19080473
    [Abstract] [Full Text] [Related]


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