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Journal Abstract Search

122 related items for PubMed ID: 21504429

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  • 6. Lateral temporal lobe epilepsies: clinical and genetic features.
    Michelucci R, Pasini E, Nobile C.
    Epilepsia; 2009 May; 50 Suppl 5():52-4. PubMed ID: 19469848
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  • 10. Drug resistant ADLTE and recurrent partial status epilepticus with dysphasic features in a family with a novel LGI1mutation: electroclinical, genetic, and EEG/fMRI findings.
    Di Bonaventura C, Carni M, Diani E, Fattouch J, Vaudano EA, Egeo G, Pantano P, Maraviglia B, Bozzao L, Manfredi M, Prencipe M, Giallonardo TA, Nobile C.
    Epilepsia; 2009 Nov; 50(11):2481-6. PubMed ID: 19552651
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  • 11. 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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  • 12. Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 gene.
    Hedera P, Abou-Khalil B, Crunk AE, Taylor KA, Haines JL, Sutcliffe JS.
    Epilepsia; 2004 Mar 05; 45(3):218-22. PubMed ID: 15009222
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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 05; 133(11):3221-31. PubMed ID: 20864493
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  • 16. Focal epilepsy of probable temporal lobe origin in a Gypsy family showing linkage to a novel locus on 7p21.3.
    Azmanov DN, Zhelyazkova S, Radionova M, Morar B, Angelicheva D, Zlatareva D, Kaneva R, Tournev I, Kalaydjieva L, Sander JW.
    Epilepsy Res; 2011 Sep 05; 96(1-2):101-8. PubMed ID: 21645995
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  • 17. Asymmetry of long-latency auditory evoked potentials in LGI1-related autosomal dominant lateral temporal lobe epilepsy.
    Brodtkorb E, Steinlein OK, Sand T.
    Epilepsia; 2005 Oct 05; 46(10):1692-4. PubMed ID: 16190946
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  • 18. A novel three base-pair LGI1 deletion leading to loss of function in a family with autosomal dominant lateral temporal epilepsy and migraine-like episodes.
    de Bellescize J, Boutry N, Chabrol E, André-Obadia N, Arzimanoglou A, Leguern E, Baulac S, Calender A, Ryvlin P, Lesca G.
    Epilepsy Res; 2009 Jul 05; 85(1):118-22. PubMed ID: 19268539
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  • 19. Screening LGI1 in a cohort of 26 lateral temporal lobe epilepsy patients with auditory aura from Turkey detects a novel de novo mutation.
    Kesim YF, Uzun GA, Yucesan E, Tuncer FN, Ozdemir O, Bebek N, Ozbek U, Iseri SA, Baykan B.
    Epilepsy Res; 2016 Feb 05; 120():73-8. PubMed ID: 26773249
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