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PUBMED FOR HANDHELDS

Journal Abstract Search


210 related items for PubMed ID: 24705833

  • 21. Rapidly progressive psychotic symptoms triggered by infection in a patient with methylenetetrahydrofolate reductase deficiency: a case report.
    Iida S, Nakamura M, Asayama S, Kunieda T, Kaneko S, Osaka H, Kusaka H.
    BMC Neurol; 2017 Feb 28; 17(1):47. PubMed ID: 28241805
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  • 23. Oxidative stress and platelet activation in subjects with moderate hyperhomocysteinaemia due to MTHFR 677 C→T polymorphism.
    Dragani A, Falco A, Santilli F, Basili S, Rolandi G, Cerasa L, Lattanzio S, Ciabattoni G, Patrono C, Davì G.
    Thromb Haemost; 2012 Sep 28; 108(3):533-42. PubMed ID: 22782530
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  • 26. Variable neurological phenotypes of homocystinuria caused by biallelic methylenetetrahydrofolate reductase variants.
    Moirangthem A, Saxena D, Masih S, Shambhavi A, Nilay M, Phadke SR.
    Clin Dysmorphol; 2022 Apr 01; 31(2):59-65. PubMed ID: 34845156
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  • 27. Severe methylenetetrahydrofolate reductase deficiency in mice results in behavioral anomalies with morphological and biochemical changes in hippocampus.
    Jadavji NM, Deng L, Leclerc D, Malysheva O, Bedell BJ, Caudill MA, Rozen R.
    Mol Genet Metab; 2012 Jun 01; 106(2):149-59. PubMed ID: 22521626
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  • 29. Stability of DNA methylation patterns in mouse spermatogonia under conditions of MTHFR deficiency and methionine supplementation.
    Garner JL, Niles KM, McGraw S, Yeh JR, Cushnie DW, Hermo L, Nagano MC, Trasler JM.
    Biol Reprod; 2013 Nov 01; 89(5):125. PubMed ID: 24048573
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  • 30. High dietary folate in pregnant mice leads to pseudo-MTHFR deficiency and altered methyl metabolism, with embryonic growth delay and short-term memory impairment in offspring.
    Bahous RH, Jadavji NM, Deng L, Cosín-Tomás M, Lu J, Malysheva O, Leung KY, Ho MK, Pallàs M, Kaliman P, Greene NDE, Bedell BJ, Caudill MA, Rozen R.
    Hum Mol Genet; 2017 Mar 01; 26(5):888-900. PubMed ID: 28069796
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  • 31. Serum folate, total homocysteine levels and methylenetetrahydrofolate reductase 677C>T polymorphism in young healthy female Japanese.
    Taguchi T, Mori H, Hamada A, Yamori Y, Mori M.
    Asia Pac J Clin Nutr; 2012 Mar 01; 21(2):291-5. PubMed ID: 22507617
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  • 33. Pearls & oy-sters: familial epileptic encephalopathy due to methylenetetrahydrofolate reductase deficiency.
    Cappuccio G, Cozzolino C, Frisso G, Romanelli R, Parenti G, D'Amico A, Carotenuto B, Salvatore F, Del Giudice E.
    Neurology; 2014 Jul 15; 83(3):e41-4. PubMed ID: 25024447
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  • 35. Plasma Homocysteine, Serum Folic Acid, Serum Vitamin B12, Serum Vitamin B6, MTHFR, and Risk of Normal-Tension Glaucoma.
    Li J, Xu F, Zeng R, Gong H, Lan Y.
    J Glaucoma; 2016 Feb 15; 25(2):e94-8. PubMed ID: 26171850
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  • 36. Insidious peripheral neuropathy occurring under treatment in infantile MTHFR deficiency.
    Chaabene-Masmoudi A, Mesrati F, Zittoun J, Landrieu P.
    J Inherit Metab Dis; 2009 Dec 15; 32 Suppl 1():S303-6. PubMed ID: 19697151
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  • 37. Homocysteine and the methylenetetrahydrofolate reductase 677C-->T polymorphism in relation to muscle mass and strength, physical performance and postural sway.
    Swart KM, Enneman AW, van Wijngaarden JP, van Dijk SC, Brouwer-Brolsma EM, Ham AC, Dhonukshe-Rutten RA, van der Velde N, Brug J, van Meurs JB, de Groot LC, Uitterlinden AG, Lips P, van Schoor NM.
    Eur J Clin Nutr; 2013 Jul 15; 67(7):743-8. PubMed ID: 23695205
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  • 38. Severe methylenetetrahydrofolate reductase deficiency: clinical clues to a potentially treatable cause of adult-onset hereditary spastic paraplegia.
    Lossos A, Teltsh O, Milman T, Meiner V, Rozen R, Leclerc D, Schwahn BC, Karp N, Rosenblatt DS, Watkins D, Shaag A, Korman SH, Heyman SN, Gal A, Newman JP, Steiner-Birmanns B, Abramsky O, Kohn Y.
    JAMA Neurol; 2014 Jul 01; 71(7):901-4. PubMed ID: 24797679
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