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PUBMED FOR HANDHELDS

Journal Abstract Search

164 related items for PubMed ID: 3087

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  • 23. Severe hyperammonemia in a newborn infant with methylmalonyl-CoA mutase deficiency.
    Packman S, Mahoney MJ, Tanaka K, Hsia YE.
    J Pediatr; 1978 May; 92(5):769-71. PubMed ID: 25314
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  • 24. The identification of (E)-2-methylglutaconic acid, a new isoleucine metabolite, in the urine of patients with beta-ketothiolase deficiency, propionic acidaemia and methylmalonic acidaemia.
    Duran M, Bruinvis L, Ketting D, Kamerling JP, Wadman SK, Schutgens RB.
    Biomed Mass Spectrom; 1982 Jan; 9(1):1-5. PubMed ID: 7059658
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  • 30. Immunochemical studies of fibroblasts from patients with methylmalonyl-CoA mutase apoenzyme deficiency: detection of a mutation interfering with mitochondrial import.
    Fenton WA, Hack AM, Kraus JP, Rosenberg LE.
    Proc Natl Acad Sci U S A; 1987 Mar; 84(5):1421-4. PubMed ID: 2881300
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  • 32. Prenatal therapy of a patient with vitamin-B12-responsive methylmalonic acidemia.
    Ampola MG, Mahoney MJ, Nakamura E, Tanaka K.
    N Engl J Med; 1975 Aug 14; 293(7):313-7. PubMed ID: 239344
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  • 33. [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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  • 34. Screening for methylmalonic aciduria in Alberta: a voluntary program with particular significance for the Hutterite Brethren.
    Fowlow SB, Holmes TM, Morgan K, Snyder FF.
    Am J Med Genet; 1985 Nov 15; 22(3):513-9. PubMed ID: 2865895
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  • 39. The occurrence of beta-hydroxy-n-valeric acid in a patient with propionic and methylmalonic acidemia.
    Stokke O, Jellum E, Eldjarn L, Schnitler R.
    Clin Chim Acta; 1973 May 30; 45(4):391-401. PubMed ID: 4730209
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