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Journal Abstract Search

544 related items for PubMed ID: 23294109

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  • 2. Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes.
    Vears DF, Tsai MH, Sadleir LG, Grinton BE, Lillywhite LM, Carney PW, Harvey AS, Berkovic SF, Scheffer IE.
    Epilepsia; 2012 Feb; 53(2):319-24. PubMed ID: 22220564
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  • 4. Atypical benign partial epilepsy/pseudo-Lennox syndrome.
    Hahn A.
    Epileptic Disord; 2000 Feb; 2 Suppl 1():S11-7. PubMed ID: 11231218
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  • 5. Atypical "benign" partial epilepsy of childhood or pseudo-lennox syndrome. Part II: family study.
    Doose H, Hahn A, Neubauer BA, Pistohl J, Stephani U.
    Neuropediatrics; 2001 Feb; 32(1):9-13. PubMed ID: 11315204
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  • 6. Family studies of individuals with eyelid myoclonia with absences.
    Sadleir LG, Vears D, Regan B, Redshaw N, Bleasel A, Scheffer IE.
    Epilepsia; 2012 Dec; 53(12):2141-8. PubMed ID: 23205932
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  • 9. Atypical "benign" partial epilepsy or pseudo-Lennox syndrome. Part I: symptomatology and long-term prognosis.
    Hahn A, Pistohl J, Neubauer BA, Stephani U.
    Neuropediatrics; 2001 Feb; 32(1):1-8. PubMed ID: 11315196
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  • 10. Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types: genomic dissection makes the link with autism.
    Lesca G, Rudolf G, Labalme A, Hirsch E, Arzimanoglou A, Genton P, Motte J, de Saint Martin A, Valenti MP, Boulay C, De Bellescize J, Kéo-Kosal P, Boutry-Kryza N, Edery P, Sanlaville D, Szepetowski P.
    Epilepsia; 2012 Sep; 53(9):1526-38. PubMed ID: 22738016
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  • 11. Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families.
    Marini C, Scheffer IE, Crossland KM, Grinton BE, Phillips FL, McMahon JM, Turner SJ, Dean JT, Kivity S, Mazarib A, Neufeld MY, Korczyn AD, Harkin LA, Dibbens LM, Wallace RH, Mulley JC, Berkovic SF.
    Epilepsia; 2004 May; 45(5):467-78. PubMed ID: 15101828
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  • 13. Benign childhood epilepsy with centrotemporal spikes and electroencephalography trait are not linked to EBN1 and EBN2 of benign neonatal familial convulsions.
    Neubauer BA, Moises HW, Lässker U, Waltz S, Diebold U, Stephani U.
    Epilepsia; 1997 Jul; 38(7):782-7. PubMed ID: 9579905
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  • 14. Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance.
    Crompton DE, Scheffer IE, Taylor I, Cook MJ, McKelvie PA, Vears DF, Lawrence KM, McMahon JM, Grinton BE, McIntosh AM, Berkovic SF.
    Brain; 2010 Nov; 133(11):3221-31. PubMed ID: 20864493
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  • 15. Magnetoencephalography localizing spike sources of atypical benign partial epilepsy.
    Shiraishi H, Haginoya K, Nakagawa E, Saitoh S, Kaneko Y, Nakasato N, Chan D, Otsubo H.
    Brain Dev; 2014 Jan; 36(1):21-7. PubMed ID: 23384398
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