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Journal Abstract Search

61 related items for PubMed ID: 22786600

  • 1. Methionine synthase deficiency: a rare cause of adult-onset leukoencephalopathy.
    Outteryck O, de Sèze J, Stojkovic T, Cuisset JM, Dobbelaere D, Delalande S, Lacour A, Cabaret M, Lepoutre AC, Deramecourt V, Zéphir H, Fowler B, Vermersch P.
    Neurology; 2012 Jul 24; 79(4):386-8. PubMed ID: 22786600
    [No Abstract] [Full Text] [Related]

  • 2. 3-Methylglutaconic aciduria type I redefined: a syndrome with late-onset leukoencephalopathy.
    Wortmann SB, Kremer BH, Graham A, Willemsen MA, Loupatty FJ, Hogg SL, Engelke UF, Kluijtmans LA, Wanders RJ, Illsinger S, Wilcken B, Cruysberg JR, Das AM, Morava E, Wevers RA.
    Neurology; 2010 Sep 21; 75(12):1079-83. PubMed ID: 20855850
    [Abstract] [Full Text] [Related]

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  • 4. [N5-methyltetrahydrofolate: homocysteine methyltransferase deficiency].
    Yoshino M.
    Ryoikibetsu Shokogun Shirizu; 1998 Sep 21; (18 Pt 1):267-8. PubMed ID: 9590043
    [No Abstract] [Full Text] [Related]

  • 5. Intractable Epilepsy due to MTR Deficiency: Importance of Homocysteine Analysis.
    Komulainen-Ebrahim J, Saastamoinen E, Rahikkala E, Helander H, Hinttala R, Risteli L, Rantala H, Uusimaa J.
    Neuropediatrics; 2017 Dec 21; 48(6):467-472. PubMed ID: 28666289
    [No Abstract] [Full Text] [Related]

  • 6. Methionine synthase deficiency: Variable clinical presentation and benefit of early diagnosis and treatment.
    Kripps KA, Sremba L, Larson AA, Van Hove JLK, Nguyen H, Wright EL, Mirsky DM, Watkins D, Rosenblatt DS, Ketteridge D, Berry SA, McCandless SE, Baker PR.
    J Inherit Metab Dis; 2022 Mar 21; 45(2):157-168. PubMed ID: 34625984
    [Abstract] [Full Text] [Related]

  • 7. [Inborn errors of amino acid metabolism--concepts and classification].
    Takita H.
    Nihon Rinsho; 1992 Jul 21; 50(7):1516-21. PubMed ID: 1404879
    [Abstract] [Full Text] [Related]

  • 8. Severe methylenetetrahydrofolate reductase deficiency, methionine synthase, and nitrous oxide--a cautionary tale.
    Erbe RW, Salis RJ.
    N Engl J Med; 2003 Jul 03; 349(1):5-6. PubMed ID: 12840086
    [No Abstract] [Full Text] [Related]

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  • 10. Neuropsychiatric illness in a patient with cobalamin G disease, an inherited disorder of vitamin B12 metabolism.
    Hill KP, Lukonis CJ, Korson MS, Weinstein C, Thall M, Schwartz JT.
    Harv Rev Psychiatry; 2004 Jul 03; 12(2):116-22. PubMed ID: 15204806
    [No Abstract] [Full Text] [Related]

  • 11. Homocystinuria.
    White HH, Thompson HL, Rowland LP, Cowen D, Araki S.
    Trans Am Neurol Assoc; 1964 Jul 03; 89():24-7. PubMed ID: 5828517
    [No Abstract] [Full Text] [Related]

  • 12. [Non-ketotic hyperglycinaemia. Clinical treatment, diet, and pathologico-anatomic changes (author's transl)].
    Leupold D, Przyrembel H, Heymer D, Hilgarth R, Krüger C, Peiffer J, Bremer HJ.
    Z Kinderheilkd; 1974 Jan 17; 116(2):95-114. PubMed ID: 4816161
    [No Abstract] [Full Text] [Related]

  • 13. Perturbation of methionine metabolism in sheep with nitrous-oxide-induced inactivation of cobalamin.
    Xue GP, Snoswell AM, Runciman WB.
    Biochem Int; 1986 Jan 17; 12(1):61-9. PubMed ID: 2868723
    [Abstract] [Full Text] [Related]

  • 14. A cobalamin metabolic defect with homocystinuria, methylmalonic aciduria and macrocytic anemia.
    Mamlok RJ, Isenberg JN, Rassin DK, Norcross K, Tallan HH.
    Neuropediatrics; 1986 May 17; 17(2):94-9. PubMed ID: 2873525
    [Abstract] [Full Text] [Related]

  • 15. Homocysteine and ischaemic heart disease.
    Law MR, Wald NJ.
    Haematologica; 1999 Jun 17; 84 Suppl EHA-4():57-60. PubMed ID: 10907469
    [No Abstract] [Full Text] [Related]

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  • 18. The inherited methylmalonic acidemias.
    Rosenberg LE.
    Prog Clin Biol Res; 1982 Jun 17; 103 Pt B():187-209. PubMed ID: 6131428
    [No Abstract] [Full Text] [Related]

  • 19. Cognitive Impairment Is Associated with AMPAR Glutamatergic Dysfunction in a Mouse Model of Neuronal Methionine Synthase Deficiency.
    Hassan Z, Coelho D, Bossenmeyer-Pourié C, Matmat K, Arnold C, Savladori A, Alberto JM, Umoret R, Guéant JL, Pourié G.
    Cells; 2023 Apr 27; 12(9):. PubMed ID: 37174668
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