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PUBMED FOR HANDHELDS

Journal Abstract Search

79 related items for PubMed ID: 3889647

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  • 3. Betaine in the treatment of homocystinuria due to 5,10-methylenetetrahydrofolate reductase deficiency.
    Wendel U, Bremer HJ.
    Eur J Pediatr; 1984 Jun; 142(2):147-50. PubMed ID: 6381059
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  • 5. Homocystinuria caused by 5,10-methylenetetrahydrofolate reductase deficiency: a case in an infant responding to methionine, folinic acid, pyridoxine, and vitamin B12 therapy.
    Harpey JP, Rosenblatt DS, Cooper BA, Le Moël G, Roy C, Lafourcade J.
    J Pediatr; 1981 Feb; 98(2):275-8. PubMed ID: 7007598
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  • 6. Betaine for treatment of homocystinuria caused by methylenetetrahydrofolate reductase deficiency.
    Holme E, Kjellman B, Ronge E.
    Arch Dis Child; 1989 Jul; 64(7):1061-4. PubMed ID: 2629632
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  • 8. Folate-responsive homocystinuria and "schizophrenia". A defect in methylation due to deficient 5,10-methylenetetrahydrofolate reductase activity.
    Freeman JM, Finkelstein JD, Mudd SH.
    N Engl J Med; 1975 Mar 06; 292(10):491-6. PubMed ID: 1117892
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  • 11. Critical review of cobalamin-folate interrelations.
    Berlow S.
    Blood; 1986 May 06; 67(5):1526. PubMed ID: 3516260
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  • 14. 5,10-Methylenetetrahydrofolate reductase deficiency. Clinical and biochemical features of a further case.
    Haan EA, Rogers JG, Lewis GP, Rowe PB.
    J Inherit Metab Dis; 1985 May 06; 8(2):53-7. PubMed ID: 3939530
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  • 17. Methylenetetrahydrofolate reductase deficiency in a patient with phenotypic findings of Angelman syndrome.
    Arn PH, Williams CA, Zori RT, Driscoll DJ, Rosenblatt DS.
    Am J Med Genet; 1998 May 18; 77(3):198-200. PubMed ID: 9605586
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  • 20. Maternal vitamin use, infant C677T mutation in MTHFR, and isolated cleft palate risk.
    Shaw GM, Todoroff K, Finnell RH, Rozen R, Lammer EJ.
    Am J Med Genet; 1999 Jul 02; 85(1):84-5. PubMed ID: 10377018
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