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PUBMED FOR HANDHELDS

Journal Abstract Search

258 related items for PubMed ID: 1404882

  • 1. [Inherited metabolic disorders of the transsulfuration pathway].
    Haraguchi H.
    Nihon Rinsho; 1992 Jul; 50(7):1548-54. PubMed ID: 1404882
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  • 9. A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida.
    Wilson A, Platt R, Wu Q, Leclerc D, Christensen B, Yang H, Gravel RA, Rozen R.
    Mol Genet Metab; 1999 Aug; 67(4):317-23. PubMed ID: 10444342
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  • 11. Two siblings with vitamin B6-nonresponsive cystathionine beta-synthase deficiency and differing blood methionine levels during the neonatal period.
    Watanabe T, Ito M, Naito E, Yokota I, Matsuda J, Kuroda Y.
    J Med Invest; 1997 Aug; 44(1-2):95-7. PubMed ID: 9395725
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  • 16. Lessons Learned from Inherited Metabolic Disorders of Sulfur-Containing Amino Acids Metabolism.
    Kožich V, Stabler S.
    J Nutr; 2020 Oct 01; 150(Suppl 1):2506S-2517S. PubMed ID: 33000152
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  • 17. Biological and environmental determinants of plasma homocysteine.
    Schneede J, Refsum H, Ueland PM.
    Semin Thromb Hemost; 2000 Oct 01; 26(3):263-79. PubMed ID: 11011844
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  • 18. Characterization of six novel mutations in the methylenetetrahydrofolate reductase (MTHFR) gene in patients with homocystinuria.
    Sibani S, Christensen B, O'Ferrall E, Saadi I, Hiou-Tim F, Rosenblatt DS, Rozen R.
    Hum Mutat; 2000 Oct 01; 15(3):280-7. PubMed ID: 10679944
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