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PUBMED FOR HANDHELDS

Journal Abstract Search


401 related items for PubMed ID: 7177670

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  • 28. Measurement of methylmalonic acid in urine filter paper specimens by gas chromatography.
    Maties M, Shih VE, Evans J, Levy HL.
    Clin Chim Acta; 1981 Aug 10; 114(2-3):303-8. PubMed ID: 7285356
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  • 32. L-Carnitine insufficiency in disorders of organic acid metabolism: response to L-carnitine by patients with methylmalonic aciduria and 3-hydroxy-3-methylglutaric aciduria.
    Chalmers RA, Stacey TE, Tracey BM, de Sousa C, Roe CR, Millington DS, Hoppel CL.
    J Inherit Metab Dis; 1984 Aug 10; 7 Suppl 2():109-10. PubMed ID: 6207380
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  • 33. High performance liquid chromatography (HPLC) method for confirming thin layer chromatography (TLC) findings in inborn errors of metabolism children in Malaysia.
    Yahya NA, Ismail Z, Embong KH, Mohamad SA.
    Southeast Asian J Trop Med Public Health; 1995 Aug 10; 26 Suppl 1():130-3. PubMed ID: 8629091
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  • 35. [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
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  • 37. Methylmalonic aciduria (cblF): case report and response to therapy.
    Waggoner DJ, Ueda K, Mantia C, Dowton SB.
    Am J Med Genet; 1998 Oct 12; 79(5):373-5. PubMed ID: 9779804
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  • 40. [The neonatal acute form of methylmalonic acidemia. Report of 2 clinical cases].
    Giardini O, Marzetti G, Lubrano R, Laurenti F, Martino F, Mannarino O, D'Eufemia P, Ruberto U.
    Minerva Pediatr; 1980 Sep 15; 32(17):1039-46. PubMed ID: 6109233
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