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Journal Abstract Search

212 related items for PubMed ID: 20152887

  • 1. Clinical and genetic evaluation of a family showing both autism and epilepsy.
    Combi R, Redaelli S, Beghi M, Clerici M, Cornaggia CM, Dalprà L.
    Brain Res Bull; 2010 Apr 29; 82(1-2):25-8. PubMed ID: 20152887
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  • 2. Autism and epilepsy: a retrospective follow-up study.
    Hara H.
    Brain Dev; 2007 Sep 29; 29(8):486-90. PubMed ID: 17321709
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  • 3. Epilepsy and mental retardation limited to females: an under-recognized disorder.
    Scheffer IE, Turner SJ, Dibbens LM, Bayly MA, Friend K, Hodgson B, Burrows L, Shaw M, Wei C, Ullmann R, Ropers HH, Szepetowski P, Haan E, Mazarib A, Afawi Z, Neufeld MY, Andrews PI, Wallace G, Kivity S, Lev D, Lerman-Sagie T, Derry CP, Korczyn AD, Gecz J, Mulley JC, Berkovic SF.
    Brain; 2008 Apr 29; 131(Pt 4):918-27. PubMed ID: 18234694
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  • 5. Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism.
    Salmon B, Hallmayer J, Rogers T, Kalaydjieva L, Petersen PB, Nicholas P, Pingree C, McMahon W, Spiker D, Lotspeich L, Kraemer H, McCague P, Dimiceli S, Nouri N, Pitts T, Yang J, Hinds D, Myers RM, Risch N.
    Am J Med Genet; 1999 Oct 15; 88(5):551-6. PubMed ID: 10490715
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  • 8. Autosomal dominant early-onset cortical myoclonus, photic-induced myoclonus, and epilepsy in a large pedigree.
    Gardella E, Tinuper P, Marini C, Guerrini R, Parrini E, Bisulli F, Liguori R, Montagna P, Lugaresi E.
    Epilepsia; 2006 Oct 15; 47(10):1643-9. PubMed ID: 17054686
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  • 13. Clinical and neurophysiological aspects of epilepsy in subjects with autism and mental retardation.
    Elia M, Musumeci SA, Ferri R, Bergonzi P.
    Am J Ment Retard; 1995 Jul 15; 100(1):6-16. PubMed ID: 7546638
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  • 14. 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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  • 19. 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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