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Journal Abstract Search

109 related items for PubMed ID: 2504657

  • 21. The effects of the immature rat model of febrile seizures on the occurrence of later generalized tonic-clonic and absence epilepsy.
    Ateş N, Akman O, Karson A.
    Brain Res Dev Brain Res; 2005 Jan 01; 154(1):137-40. PubMed ID: 15617762
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  • 22. Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3.
    Hedera P, Blair MA, Andermann E, Andermann F, D'Agostino D, Taylor KA, Chahine L, Pandolfo M, Bradford Y, Haines JL, Abou-Khalil B.
    Neurology; 2007 Jun 12; 68(24):2107-12. PubMed ID: 17377072
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  • 23. Atypical benign partial epilepsy/pseudo-Lennox syndrome.
    Hahn A.
    Epileptic Disord; 2000 Jun 12; 2 Suppl 1():S11-7. PubMed ID: 11231218
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  • 27. GEFS+ where focal seizures evolve from generalized spike wave: video-EEG study of two children.
    Deng YH, Berkovic SF, Scheffer IE.
    Epileptic Disord; 2007 Sep 12; 9(3):307-14. PubMed ID: 17884755
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  • 28. Mapping and positional cloning of common idiopathic generalized epilepsies: juvenile myoclonus epilepsy and childhood absence epilepsy.
    Delgado-Escueta AV, Medina MT, Serratosa JM, Castroviejo IP, Gee MN, Weissbecker K, Westling BW, Fong CY, Alonso ME, Cordova S, Shah P, Khan S, Sainz J, Rubio-Donnadieu F, Sparkes RS.
    Adv Neurol; 1999 Sep 12; 79():351-74. PubMed ID: 10514826
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  • 30. [Epilepsies and febrile convulsions].
    Lagenstein I, Stahnke N.
    Nervenarzt; 1984 Apr 12; 55(4):173-8. PubMed ID: 6427636
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  • 31. Familial occipitotemporal lobe epilepsy and migraine with visual aura: linkage to chromosome 9q.
    Deprez L, Peeters K, Van Paesschen W, Claeys KG, Claes LR, Suls A, Audenaert D, Van Dyck T, Goossens D, Del-Favero J, De Jonghe P.
    Neurology; 2007 Jun 05; 68(23):1995-2002. PubMed ID: 17460155
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  • 32. Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation.
    Lebas A, Guyant-Maréchal L, Hannequin D, Riant F, Tournier-Lasserve E, Parain D.
    Cephalalgia; 2008 Jul 05; 28(7):774-7. PubMed ID: 18498390
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  • 33. [Idiopathic partial epilepsy with occipital paroxysms].
    Martinović Z.
    Srp Arh Celok Lek; 1999 Jul 05; 127(7-8):241-8. PubMed ID: 10624397
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  • 34. 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 05; 110(1):27-38. PubMed ID: 15180804
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  • 35. Febrile convulsions followed by nonfebrile convulsions. A clinical, electroencephalographic and follow-up study.
    Tsuboi T, Endo S.
    Neuropadiatrie; 1977 Aug 05; 8(3):209-23. PubMed ID: 408736
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  • 36. 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 05; 45(5):467-78. PubMed ID: 15101828
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  • 37. Clinical investigation of genetic contributions to childhood-onset epilepsies and epileptic syndromes.
    Wakamoto H, Hayashi M, Nagao H, Morimoto T, Kida K.
    Brain Dev; 2004 Apr 05; 26(3):184-9. PubMed ID: 15030907
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  • 38. Three new forms of familial epilepsy syndromes in the proposed diagnostic scheme of the ILAE (2001): a clinical experience in Southwest China.
    Lu Y, Yu W, Shen D, Wang X.
    Epilepsia; 2008 Jun 05; 49(6):1103. PubMed ID: 18554358
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  • 40. Familial temporal lobe epilepsy: a clinically heterogeneous syndrome.
    Cendes F, Lopes-Cendes I, Andermann E, Andermann F.
    Neurology; 1998 Feb 05; 50(2):554-7. PubMed ID: 9484399
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