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Journal Abstract Search

163 related items for PubMed ID: 36732069

  • 1. Cerebral Creatine Deficiency Affects the Timing of Oligodendrocyte Myelination.
    Rosko LM, Gentile T, Smith VN, Manavi Z, Melchor GS, Hu J, Shults NV, Albanese C, Lee Y, Rodriguez O, Huang JK.
    J Neurosci; 2023 Feb 15; 43(7):1143-1153. PubMed ID: 36732069
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  • 4. Loss of Tuberous Sclerosis Complex1 in Adult Oligodendrocyte Progenitor Cells Enhances Axon Remyelination and Increases Myelin Thickness after a Focal Demyelination.
    McLane LE, Bourne JN, Evangelou AV, Khandker L, Macklin WB, Wood TL.
    J Neurosci; 2017 Aug 02; 37(31):7534-7546. PubMed ID: 28694334
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  • 5. ClinGen variant curation expert panel recommendations for classification of variants in GAMT, GATM and SLC6A8 for cerebral creatine deficiency syndromes.
    Goldstein J, Thomas-Wilson A, Groopman E, Aggarwal V, Bianconi S, Fernandez R, Hart K, Longo N, Liang N, Reich D, Wallis H, Weaver M, Young S, Mercimek-Andrews S.
    Mol Genet Metab; 2024 May 02; 142(1):108362. PubMed ID: 38452609
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  • 6. Olig2 Ablation in Immature Oligodendrocytes Does Not Enhance CNS Myelination and Remyelination.
    Wang J, Yang L, Jiang M, Zhao C, Liu X, Berry K, Waisman A, Langseth AJ, Novitch BG, Bergles DE, Nishiyama A, Lu QR.
    J Neurosci; 2022 Nov 09; 42(45):8542-8555. PubMed ID: 36198499
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  • 7. Cell-Type-Specific Spatiotemporal Expression of Creatine Biosynthetic Enzyme S-adenosylmethionine:guanidinoacetate N-methyltransferase in Developing Mouse Brain.
    Tachikawa M, Watanabe M, Fukaya M, Sakai K, Terasaki T, Hosoya KI.
    Neurochem Res; 2018 Feb 09; 43(2):500-510. PubMed ID: 29209878
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  • 9. Apoptosis of Oligodendrocytes during Early Development Delays Myelination and Impairs Subsequent Responses to Demyelination.
    Caprariello AV, Batt CE, Zippe I, Romito-DiGiacomo RR, Karl M, Miller RH.
    J Neurosci; 2015 Oct 14; 35(41):14031-41. PubMed ID: 26468203
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  • 10. Evidence-based treatment of guanidinoacetate methyltransferase (GAMT) deficiency.
    Viau KS, Ernst SL, Pasquali M, Botto LD, Hedlund G, Longo N.
    Mol Genet Metab; 2013 Nov 14; 110(3):255-62. PubMed ID: 24071436
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  • 15. Guanidinoacetate N-methyltransferase deficiency: Case report and brief review of the literature.
    Libell JL, Lakhani DA, Balar AB, Khan M, Carpenter JS, Joseph JT.
    Radiol Case Rep; 2023 Dec 14; 18(12):4331-4337. PubMed ID: 37808418
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  • 16. Intellectual Disability and Brain Creatine Deficit: Phenotyping of the Genetic Mouse Model for GAMT Deficiency.
    Rossi L, Nardecchia F, Pierigè F, Ventura R, Carducci C, Leuzzi V, Magnani M, Cabib S, Pascucci T.
    Genes (Basel); 2021 Aug 02; 12(8):. PubMed ID: 34440375
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  • 17. Inborn errors of creatine metabolism and epilepsy.
    Leuzzi V, Mastrangelo M, Battini R, Cioni G.
    Epilepsia; 2013 Feb 02; 54(2):217-27. PubMed ID: 23157605
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  • 19. Novel guanidinoacetate methyltransferase (GAMT) mutation associated with cerebral creatine deficiency syndrome in a Syrian child: a case report.
    Alhomsi D, Abdalsalam D, Sulaiman R, Bakleh S, Alasmar D.
    Ann Med Surg (Lond); 2023 May 02; 85(5):1906-1910. PubMed ID: 37228909
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