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Journal Abstract Search

313 related items for PubMed ID: 22029951

  • 1. Clinical spectrum of SCN2A mutations.
    Shi X, Yasumoto S, Kurahashi H, Nakagawa E, Fukasawa T, Uchiya S, Hirose S.
    Brain Dev; 2012 Aug; 34(7):541-5. PubMed ID: 22029951
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  • 5. Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?
    Scheffer IE, Zhang YH, Jansen FE, Dibbens L.
    Brain Dev; 2009 May; 31(5):394-400. PubMed ID: 19203856
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  • 6. Neonatal epilepsy syndromes and GEFS+: mechanistic considerations.
    Burgess DL.
    Epilepsia; 2005 May; 46 Suppl 10():51-8. PubMed ID: 16359473
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  • 9. Clinical spectrum of SCN1A mutations.
    Gambardella A, Marini C.
    Epilepsia; 2009 May; 50 Suppl 5():20-3. PubMed ID: 19469841
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  • 14. Infantile epilepsy associated with mosaic 2q24 duplication including SCN2A and SCN3A.
    Vecchi M, Cassina M, Casarin A, Rigon C, Drigo P, De Palma L, Clementi M.
    Seizure; 2011 Dec; 20(10):813-6. PubMed ID: 21893419
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  • 17. Variable epilepsy phenotypes associated with a familial intragenic deletion of the SCN1A gene.
    Guerrini R, Cellini E, Mei D, Metitieri T, Petrelli C, Pucatti D, Marini C, Zamponi N.
    Epilepsia; 2010 Dec; 51(12):2474-7. PubMed ID: 21204810
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  • 19. Epilepsy with a de novo missense mutation in the sodium channel a1 subunit: a case report.
    Stefanaki E, Aggelakou V, Orfanou M, Kokori E, Boutoufianakis S.
    Acta Paediatr; 2006 Dec; 95(12):1703-6. PubMed ID: 17129991
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