These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

99 related items for PubMed ID: 6145531

  • 1. A radio-HPLC assay for the measurement of methylmalonyl-CoA mutase.
    Causey AG, Bartlett K.
    Clin Chim Acta; 1984 May 30; 139(2):179-86. PubMed ID: 6145531
    [No Abstract] [Full Text] [Related]

  • 2. 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 30; 123(1):1-8. PubMed ID: 21471
    [Abstract] [Full Text] [Related]

  • 3. Methylmalonic acidaemia: haplotype analysis of the methylmalonyl-CoA-mutase gene in Europe.
    Bender C, Büchler A, Baumgartner R, Konecki DS, Trefz FK.
    Eur J Pediatr; 1994 Jun 30; 153(6):468. PubMed ID: 7916290
    [No Abstract] [Full Text] [Related]

  • 4. [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
    [No Abstract] [Full Text] [Related]

  • 5. 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 15; 21(6):553-67. PubMed ID: 12939
    [Abstract] [Full Text] [Related]

  • 6. 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 15; 15(3):241-5. PubMed ID: 11786
    [No Abstract] [Full Text] [Related]

  • 7. Assay of methylmalonyl CoA mutase with high-performance liquid chromatography.
    Kikuchi M, Hanamizu H, Narisawa K, Tada K.
    Clin Chim Acta; 1989 Oct 16; 184(3):307-13. PubMed ID: 2575466
    [Abstract] [Full Text] [Related]

  • 8. Novel mutation of methylmalonyl-CoA mutase gene causing the mut0 form of methylmalonic acidemia in a Japanese girl.
    Oyama C, Takahashi T, Matsumori M, Shoji Y, Tajima G, Sakura N, Hasegawa Y, Yamaguchi S, Kakinuma H, Takada G.
    Pediatr Int; 2007 Apr 16; 49(2):232-4. PubMed ID: 17445044
    [No Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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]

  • 11. Methylmalonic acidemia.
    Cohen JJ.
    Kidney Int; 1979 Mar 03; 15(3):311-20. PubMed ID: 41966
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Long-term follow-up of 77 patients with isolated methylmalonic acidaemia.
    Baumgarter ER, Viardot C.
    J Inherit Metab Dis; 1995 Mar 03; 18(2):138-42. PubMed ID: 7564229
    [No Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Methylmalonyl CoA mutase--a radiochromatographic assay.
    Goodey PA, Gompertz D.
    Clin Chim Acta; 1972 Nov 01; 42(1):119-23. PubMed ID: 4654847
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. [Isolated methylmalonyl-CoA mutase deficiency].
    Yoshino M.
    Ryoikibetsu Shokogun Shirizu; 1998 Nov 01; (18 Pt 1):269-72. PubMed ID: 9590044
    [No Abstract] [Full Text] [Related]

  • 18. Towards metabolic sink therapy for mut methylmalonic acidaemia: retrovirus-mediated transfer of the human methylmalonyl-CoA mutase cDNA into peripheral blood progenitor cells of a child with mut methylmalonic acidaemia.
    Chang CC, Hsiao KJ, Chen ML, Lin CM.
    J Inherit Metab Dis; 1999 Dec 01; 22(8):951-2. PubMed ID: 10604156
    [No Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. Liver transplantation is not curative for methylmalonic acidopathy caused by methylmalonyl-CoA mutase deficiency.
    Kaplan P, Ficicioglu C, Mazur AT, Palmieri MJ, Berry GT.
    Mol Genet Metab; 2006 Aug 05; 88(4):322-6. PubMed ID: 16750411
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.