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543 related items for PubMed ID: 23294109

  • 1. Clinical genetic study of the epilepsy-aphasia spectrum.
    Tsai MH, Vears DF, Turner SJ, Smith RL, Berkovic SF, Sadleir LG, Scheffer IE.
    Epilepsia; 2013 Feb; 54(2):280-7. PubMed ID: 23294109
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 3. GRIN2A mutations in epilepsy-aphasia spectrum disorders.
    Yang X, Qian P, Xu X, Liu X, Wu X, Zhang Y, Yang Z.
    Brain Dev; 2018 Mar; 40(3):205-210. PubMed ID: 29056244
    [Abstract] [Full Text] [Related]

  • 4. Atypical benign partial epilepsy/pseudo-Lennox syndrome.
    Hahn A.
    Epileptic Disord; 2000 Mar; 2 Suppl 1():S11-7. PubMed ID: 11231218
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 7. Seizures among families of Indian probands with different epileptic syndromes.
    Jain S, Bhatia M, Tripathi M, Srivastava A, Padma MV, Pandey RM.
    Acta Neurol Scand; 2004 Jul; 110(1):27-38. PubMed ID: 15180804
    [Abstract] [Full Text] [Related]

  • 8. Familial genetic predisposition, epilepsy localization and antecedent febrile seizures.
    Abou-Khalil B, Krei L, Lazenby B, Harris PA, Haines JL, Hedera P.
    Epilepsy Res; 2007 Jan; 73(1):104-10. PubMed ID: 17046202
    [Abstract] [Full Text] [Related]

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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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 12. From rolandic epilepsy to continuous spike-and-waves during sleep and Landau-Kleffner syndromes: insights into possible genetic factors.
    Rudolf G, Valenti MP, Hirsch E, Szepetowski P.
    Epilepsia; 2009 Aug; 50 Suppl 7():25-8. PubMed ID: 19682046
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 16. [Epileptic syndromes which show continuous spike and wake complexes during slow wave sleep].
    Nieto-Barrera M, Aguilar-Quero F, Montes E, Candau R, Prieto P.
    Rev Neurol; 1997 Jul; 25(143):1045-51. PubMed ID: 9280631
    [Abstract] [Full Text] [Related]

  • 17. Update on the genetics of the epilepsy-aphasia spectrum and role of GRIN2A mutations.
    Lesca G, Møller RS, Rudolf G, Hirsch E, Hjalgrim H, Szepetowski P.
    Epileptic Disord; 2019 Jun 01; 21(S1):41-47. PubMed ID: 31149903
    [Abstract] [Full Text] [Related]

  • 18. Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region.
    Reutlinger C, Helbig I, Gawelczyk B, Subero JI, Tönnies H, Muhle H, Finsterwalder K, Vermeer S, Pfundt R, Sperner J, Stefanova I, Gillessen-Kaesbach G, von Spiczak S, van Baalen A, Boor R, Siebert R, Stephani U, Caliebe A.
    Epilepsia; 2010 Sep 01; 51(9):1870-3. PubMed ID: 20384727
    [Abstract] [Full Text] [Related]

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  • 20. Benign occipital epilepsies of childhood: clinical features and genetics.
    Taylor I, Berkovic SF, Kivity S, Scheffer IE.
    Brain; 2008 Sep 01; 131(Pt 9):2287-94. PubMed ID: 18669497
    [Abstract] [Full Text] [Related]

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