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551 related items for PubMed ID: 12861512

  • 1. [Severe myoclonic epilepsy in infancy (Dravet's syndrome). Its nosological characteristics and therapeutic aspects].
    Nieto Barrera M, Candau Fernandez Mensaque R, Nieto Jiménez M.
    Rev Neurol; ; 37(1):64-8. PubMed ID: 12861512
    [Abstract] [Full Text] [Related]

  • 2. [Severe myoclonic epilepsy in infancy (Dravet's syndrome). Some genetic aspects].
    Herranz JL.
    Rev Neurol; ; 37(1):60-3. PubMed ID: 12861511
    [Abstract] [Full Text] [Related]

  • 3. [Clinical and genetic diagnosis of Dravet syndrome: report of 20 cases].
    Siegler Z, Neuwirth M, Hegyi M, Paraicz E, Pálmafy B, Tegzes A, Barsi P, Karcagi V, Claes L, De Jonghe P, Herczegfalvi A, Fogarasi A.
    Ideggyogy Sz; 2008 Nov 30; 61(11-12):402-8. PubMed ID: 19070316
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  • 4. Clinical spectrum of mutations in SCN1A gene: severe myoclonic epilepsy in infancy and related epilepsies.
    Fujiwara T.
    Epilepsy Res; 2006 Aug 30; 70 Suppl 1():S223-30. PubMed ID: 16806826
    [Abstract] [Full Text] [Related]

  • 5. Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy.
    Ceulemans BP, Claes LR, Lagae LG.
    Pediatr Neurol; 2004 Apr 30; 30(4):236-43. PubMed ID: 15087100
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  • 6. [Epilepsy beginning in the neonatal period and early infancy].
    Ruggieri VL.
    Rev Neurol; 2004 Apr 30; 39(3):251-62. PubMed ID: 15284967
    [Abstract] [Full Text] [Related]

  • 7. "Severe myoclonic epilepsy in infancy". Relevance for the clinician of severe epilepsy starting in infancy.
    Ceulemans B, Cras P.
    Acta Neurol Belg; 2004 Sep 30; 104(3):95-9. PubMed ID: 15508261
    [Abstract] [Full Text] [Related]

  • 8. Myoclonic-astatic epilepsy.
    Doose H.
    Epilepsy Res Suppl; 1992 Sep 30; 6():163-8. PubMed ID: 1418479
    [Abstract] [Full Text] [Related]

  • 9. The natural history of myoclonic astatic epilepsy (Doose syndrome) and Lennox-Gastaut syndrome.
    Stephani U.
    Epilepsia; 2006 Sep 30; 47 Suppl 2():53-5. PubMed ID: 17105462
    [Abstract] [Full Text] [Related]

  • 10. [Severe myoclonic epilepsy in infancy. Clinical and paraclinical aspects].
    Martínez-Bermejo A, López-Martín V, Arcas J, Tendero A, Roche Herrero MC, Merino M.
    Rev Neurol; 2006 Sep 30; 37(1):55-9. PubMed ID: 12861510
    [Abstract] [Full Text] [Related]

  • 11. Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identified.
    Zucca C, Redaelli F, Epifanio R, Zanotta N, Romeo A, Lodi M, Veggiotti P, Airoldi G, Panzeri C, Romaniello R, De Polo G, Bonanni P, Cardinali S, Baschirotto C, Martorell L, Borgatti R, Bresolin N, Bassi MT.
    Arch Neurol; 2008 Apr 30; 65(4):489-94. PubMed ID: 18413471
    [Abstract] [Full Text] [Related]

  • 12. Debate: Does genetic information in humans help us treat patients? PRO--genetic information in humans helps us treat patients. CON--genetic information does not help at all.
    Delgado-Escueta AV, Bourgeois BF.
    Epilepsia; 2008 Dec 30; 49 Suppl 9():13-24. PubMed ID: 19087113
    [Abstract] [Full Text] [Related]

  • 13. Genetics of myoclonic and myoclonus epilepsies.
    Minassian BA, Sainz J, Delgado-Escueta AV.
    Clin Neurosci; 2008 Dec 30; 3(4):223-35. PubMed ID: 8891396
    [Abstract] [Full Text] [Related]

  • 14. A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures.
    Kimura K, Sugawara T, Mazaki-Miyazaki E, Hoshino K, Nomura Y, Tateno A, Hachimori K, Yamakawa K, Segawa M.
    Brain Dev; 2005 Sep 30; 27(6):424-30. PubMed ID: 16122630
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  • 17. Familial severe myoclonic epilepsy of infancy: truncation of Nav1.1 and genetic heterogeneity.
    Gennaro E, Veggiotti P, Malacarne M, Madia F, Cecconi M, Cardinali S, Cassetti A, Cecconi I, Bertini E, Bianchi A, Gobbi G, Zara F.
    Epileptic Disord; 2003 Mar 30; 5(1):21-5. PubMed ID: 12773292
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  • 20. Stiripentol: new preparation. Severe myoclonic epilepsy of infancy: promising.
    Prescrire Int; 2005 Apr 30; 14(76):57-9. PubMed ID: 15875342
    [Abstract] [Full Text] [Related]

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