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Journal Abstract Search

137 related items for PubMed ID: 23593750

  • 1. [Successful treatment with levetiracetam in a case of Ohtahara syndrome caused by STXBP1 mutation].
    Yamashita S, Chiyonobu T, Yoshida M, Moroto M, Morita T, Morioka S, Kato M, Saitsu H, Morimoto M, Hosoi H.
    No To Hattatsu; 2013 Jan; 45(1):64-6. PubMed ID: 23593750
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  • 2. Dramatic effect of levetiracetam in early-onset epileptic encephalopathy due to STXBP1 mutation.
    Dilena R, Striano P, Traverso M, Viri M, Cristofori G, Tadini L, Barbieri S, Romeo A, Zara F.
    Brain Dev; 2016 Jan; 38(1):128-31. PubMed ID: 26212315
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  • 5. Phenytoin neurotoxicity in a child carrying new STXBP1 and CYP2C9 gene mutations.
    Guacci A, Chetta M, Rizzo F, Marchese G, De Filippo MR, Giurato G, Nassa G, Ravo M, Tarallo R, Rocco T, Operto FF, Weisz A, Coppola G.
    Seizure; 2016 Jan; 34():26-8. PubMed ID: 26658169
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  • 13. Efficacy and tolerability of levetiracetam in children with epilepsy.
    Li J, Xiao N, Chen S.
    Brain Dev; 2011 Feb; 33(2):145-51. PubMed ID: 20359839
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  • 18. Novel mutation in STXBP1 gene in a patient with non-lesional Ohtahara syndrome.
    Ortega-Moreno L, Giráldez BG, Verdú A, García-Campos O, Sánchez-Martín G, Serratosa JM, Guerrero-López R.
    Neurologia; 2016 Oct; 31(8):523-7. PubMed ID: 25631041
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