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Journal Abstract Search

390 related items for PubMed ID: 8232778

  • 1. Exclusion of linkage of genetic focal sharp waves to the HLA region on chromosome 6p in families with benign partial epilepsy with centrotemporal sharp waves.
    Whitehouse W, Diebold U, Rees M, Parker K, Doose H, Gardiner RM.
    Neuropediatrics; 1993 Aug; 24(4):208-10. PubMed ID: 8232778
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  • 2. Benign childhood epilepsy with centrotemporal spikes and the focal sharp wave trait is not linked to the fragile X region.
    Rees M, Diebold U, Parker K, Doose H, Gardiner RM, Whitehouse WP.
    Neuropediatrics; 1993 Aug; 24(4):211-3. PubMed ID: 8232779
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  • 4. The phenotypic spectrum related to the human epilepsy susceptibility gene "EJM1".
    Sander T, Hildmann T, Janz D, Wienker TF, Neitzel H, Bianchi A, Bauer G, Sailer U, Berek K, Schmitz B.
    Ann Neurol; 1995 Aug; 38(2):210-7. PubMed ID: 7654068
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  • 5. Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6.
    Weissbecker KA, Durner M, Janz D, Scaramelli A, Sparkes RS, Spence MA.
    Am J Med Genet; 1991 Jan; 38(1):32-6. PubMed ID: 1901452
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  • 6. 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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  • 9. 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 05; 38(7):782-7. PubMed ID: 9579905
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  • 10. Partial epilepsy with pericentral spikes: a new familial epilepsy syndrome with evidence for linkage to chromosome 4p15.
    Kinton L, Johnson MR, Smith SJ, Farrell F, Stevens J, Rance JB, Claudino AM, Duncan JS, Davis MB, Wood NW, Sander JW.
    Ann Neurol; 2002 Jun 05; 51(6):740-9. PubMed ID: 12112080
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  • 11. Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region.
    Whitehouse WP, Rees M, Curtis D, Sundqvist A, Parker K, Chung E, Baralle D, Gardiner RM.
    Am J Hum Genet; 1993 Sep 05; 53(3):652-62. PubMed ID: 8352275
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  • 12. Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12.
    Berkovic SF, Serratosa JM, Phillips HA, Xiong L, Andermann E, Díaz-Otero F, Gómez-Garre P, Martín M, Fernández-Bullido Y, Andermann F, Lopes-Cendes I, Dubeau F, Desbiens R, Scheffer IE, Wallace RH, Mulley JC, Pandolfo M.
    Epilepsia; 2004 Sep 05; 45(9):1054-60. PubMed ID: 15329069
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  • 15. Clinical and genetic analysis of a large pedigree with juvenile myoclonic epilepsy.
    Serratosa JM, Delgado-Escueta AV, Medina MT, Zhang Q, Iranmanesh R, Sparkes RS.
    Ann Neurol; 1996 Feb 05; 39(2):187-95. PubMed ID: 8967750
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  • 16. 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 05; 133(11):3221-31. PubMed ID: 20864493
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  • 17. Genetic focal epilepsies: state of the art and paths to the future.
    Andermann F, Kobayashi E, Andermann E.
    Epilepsia; 2005 Nov 05; 46 Suppl 10():61-7. PubMed ID: 16359475
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  • 18. No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1.
    Sander T, Windemuth C, Schulz H, Saar K, Gennaro E, Bianchi A, Zara F, Bulteau C, Kaminska A, Ville D, Cieuta C, Prud'homme JF, Dulac O, Bate L, Gardiner RM, de Haan GJ, Janssen GA, Witte J, Halley DJ, Lindhout D, Wienker TF, Janz D, European Consortium on the Genetics of Idiopathic Generalized Epilepsy.
    Am J Med Genet; 2002 Aug 08; 114(6):673-8. PubMed ID: 12210286
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  • 19. Common subtypes of idiopathic generalized epilepsies: lack of linkage to D20S19 close to candidate loci (EBN1, EEGV1) on chromosome 20.
    Sander T, Hildmann T, Wienker TF, Ramel C, Beck-Mannagetta G, Bianchi A, Sailer U, Berek K, Bauer G, Neitzel H, Schmitz B, Durner M, Johnson KJ, Janz D.
    Am J Med Genet; 1996 Feb 16; 67(1):31-9. PubMed ID: 8678111
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