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Journal Abstract Search

164 related items for PubMed ID: 3087

  • 1. A case of methylmalonic and propionic acidemia due to methulmalonyl-CoA carbonylmutase apoenzyme deficiency.
    van den Berg H, Boelkens MT, Hommes FA.
    Acta Paediatr Scand; 1976 Jan; 65(1):113-8. PubMed ID: 3087
    [Abstract] [Full Text] [Related]

  • 2. Methylmalonic acidemia.
    Matsuda I, Terashima T, Yamamoto J, Akaboshi I, Shinozuka S, Hattori S, Nagata N, Oka Y.
    Eur J Pediatr; 1978 Jul 03; 128(3):181-6. PubMed ID: 27367
    [Abstract] [Full Text] [Related]

  • 3. A new variant of methylmalonic acidemia-defective coenzyme-apoenzyme binding in cultured fibroblasts.
    Morrow G, Revsin B, Clark R, Lebowitz J, Whelan DT.
    Clin Chim Acta; 1978 Apr 03; 85(1):67-72. PubMed ID: 25730
    [Abstract] [Full Text] [Related]

  • 4. Studies of methylmalonyl coenzyme A carbonylmutase activity in methylmalonic acidemia. I. Correlation of clinical, hepatic, and fibroblast data.
    Morrow G, Mahoney MJ, Mathews C, Lebowitz J.
    Pediatr Res; 1975 Aug 03; 9(8):641-4. PubMed ID: 239382
    [Abstract] [Full Text] [Related]

  • 5. Methylmalonic aciduria: a variant form of methylmalonyl coenzyme A apomutase deficiency.
    Wilcken B, Kilham HA, Faull K.
    J Pediatr; 1977 Sep 03; 91(3):428-30. PubMed ID: 19569
    [Abstract] [Full Text] [Related]

  • 6. Immunochemical studies on cultured fibroblasts from patients with inherited methylmalonic acidemia.
    Kolhouse JF, Utley C, Fenton WA, Rosenberg LE.
    Proc Natl Acad Sci U S A; 1981 Dec 03; 78(12):7737-41. PubMed ID: 6121323
    [Abstract] [Full Text] [Related]

  • 7. Studies of methylmalonyl-coenzyme A carbonylmutase activity in methylmalonic acidemia. II. In vitro binding kinetics with adenosylcobalamin.
    Morrow G, Lebowitz J.
    Biochem Med; 1976 Jun 03; 15(3):241-5. PubMed ID: 11786
    [No Abstract] [Full Text] [Related]

  • 8. Benign methylmalonic aciduria.
    Ledley FD, Levy HL, Shih VE, Benjamin R, Mahoney MJ.
    N Engl J Med; 1984 Oct 18; 311(16):1015-8. PubMed ID: 6148691
    [Abstract] [Full Text] [Related]

  • 9. Inhibition by propionyl-coenzyme A of N-acetylglutamate synthetase in rat liver mitochondria. A possible explanation for hyperammonemia in propionic and methylmalonic acidemia.
    Coude FX, Sweetman L, Nyhan WL.
    J Clin Invest; 1979 Dec 18; 64(6):1544-51. PubMed ID: 500823
    [Abstract] [Full Text] [Related]

  • 10. Biochemical and anaplerotic applications of in vitro models of propionic acidemia and methylmalonic acidemia using patient-derived primary hepatocytes.
    Collado MS, Armstrong AJ, Olson M, Hoang SA, Day N, Summar M, Chapman KA, Reardon J, Figler RA, Wamhoff BR.
    Mol Genet Metab; 2020 Jul 18; 130(3):183-196. PubMed ID: 32451238
    [Abstract] [Full Text] [Related]

  • 11. Comparison of cytosolic and mitochondrial enzyme alterations in the livers of propionic or methylmalonic acidemia: a reduction of cytochrome oxidase activity.
    Hayasaka K, Metoki K, Satoh T, Narisawa K, Tada K, Kawakami T, Matsuo N, Aoki T.
    Tohoku J Exp Med; 1982 Jul 18; 137(3):329-34. PubMed ID: 6287671
    [Abstract] [Full Text] [Related]

  • 12. Studies on the urinary acidic metabolites from three patients with methylmalonic aciduria.
    Kuhara T, Matsumoto I.
    Biomed Mass Spectrom; 1980 Oct 18; 7(10):424-8. PubMed ID: 6111361
    [Abstract] [Full Text] [Related]

  • 13. Methylmalonic/beta-hydroxy-n-valeric aciduria due to methylmalonyl-CoA mutase deficiency.
    Goodman SI, McCabe ER, Fennessey PV, Miles BS, Mace JW, Jellum E.
    Clin Chim Acta; 1978 Aug 01; 87(3):441-9. PubMed ID: 28187
    [Abstract] [Full Text] [Related]

  • 14. Methylmalonyl-CoA mutase activity of leukocytes in variants and heterozygotes of methylmalonic acidemia.
    Narisawa K, Saito T, Hisa S, Suzuki H, Hayasaka K.
    Tohoku J Exp Med; 1977 Sep 01; 123(1):1-8. PubMed ID: 21471
    [Abstract] [Full Text] [Related]

  • 15. Congenital methylmalonic acidemia: a variant of the B12 'non-responsive' form with evidence for reduced affinity of methylmalonyl-CoA mutase for its B12-coenzyme.
    Baumgartner ER, Bachmann C, Wick H.
    Enzyme; 1976 Sep 01; 21(6):553-67. PubMed ID: 12939
    [Abstract] [Full Text] [Related]

  • 16. Biochemical analysis of intact fibroblasts from two cases with methylmalonic acidaemia.
    Kakinuma H, Ogura N, Ohtake A, Takayanagi M, Nakajima H, Kondo H, Terada H, Okuda K, Nomoto Y.
    J Inherit Metab Dis; 1985 Sep 01; 8(3):151-2. PubMed ID: 2879965
    [No Abstract] [Full Text] [Related]

  • 17. Identification of methyl-branched chain dicarboxylic acids in amniotic fluid and urine in propionic and methylmalonic acidemia.
    Jakobs C, Dorland L, Sweetman L, Duran M, Nyhan WL, Wadman SK.
    Pediatr Res; 1984 Nov 01; 18(11):1185-91. PubMed ID: 6514446
    [Abstract] [Full Text] [Related]

  • 18. Methylmalonic aciduria without vitamin B12 deficiency in an adult sibship.
    Giorgio AJ, Trowbridge M, Boone AW, Patten RS.
    N Engl J Med; 1976 Aug 05; 295(6):310-3. PubMed ID: 6909
    [Abstract] [Full Text] [Related]

  • 19. Propionyl-CoA and adenosylcobalamin metabolism in Caenorhabditis elegans: evidence for a role of methylmalonyl-CoA epimerase in intermediary metabolism.
    Chandler RJ, Aswani V, Tsai MS, Falk M, Wehrli N, Stabler S, Allen R, Sedensky M, Kazazian HH, Venditti CP.
    Mol Genet Metab; 2006 Aug 05; 89(1-2):64-73. PubMed ID: 16843692
    [Abstract] [Full Text] [Related]

  • 20. Methylmalonic and propionic acidemias: lipid profiles of normal and affected human skin fibroblasts incubated with [1-14C]propionate.
    Giudici TA, Chen RG, Oizumi J, Shaw KN, Ng WG, Donnell GN.
    Biochem Med Metab Biol; 1986 Jun 05; 35(3):384-98. PubMed ID: 2872907
    [Abstract] [Full Text] [Related]

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