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Journal Abstract Search

163 related items for PubMed ID: 23651915

  • 21. Seizure semiology in autosomal dominant epilepsy with auditory features, due to novel LGI1 mutations.
    Sadleir LG, Agher D, Chabrol E, Elkouby L, Leguern E, Paterson SJ, Harty R, Bellows ST, Berkovic SF, Scheffer IE, Baulac S.
    Epilepsy Res; 2013 Dec; 107(3):311-7. PubMed ID: 24206907
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  • 22. Induced pluripotent stem cells derived from an autosomal dominant lateral temporal epilepsy (ADLTE) patient carrying S473L mutation in leucine-rich glioma inactivated 1 (LGI1).
    Tan GW, Kondo T, Murakami N, Imamura K, Enami T, Tsukita K, Shibukawa R, Funayama M, Matsumoto R, Ikeda A, Takahashi R, Inoue H.
    Stem Cell Res; 2017 Oct; 24():12-15. PubMed ID: 29034879
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  • 23. Abnormal phonologic processing in familial lateral temporal lobe epilepsy due to a new LGI1 mutation.
    Pisano T, Marini C, Brovedani P, Brizzolara D, Pruna D, Mei D, Moro F, Cianchetti C, Guerrini R.
    Epilepsia; 2005 Jan; 46(1):118-23. PubMed ID: 15660777
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  • 24. 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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  • 28. No evidence for a seriously increased malignancy risk in LGI1-caused epilepsy.
    Brodtkorb E, Nakken KO, Steinlein OK.
    Epilepsy Res; 2003 Oct; 56(2-3):205-8. PubMed ID: 14643004
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  • 29. LGI1 microdeletion in autosomal dominant lateral temporal epilepsy.
    Fanciulli M, Santulli L, Errichiello L, Barozzi C, Tomasi L, Rigon L, Cubeddu T, de Falco A, Rampazzo A, Michelucci R, Uzzau S, Striano S, de Falco FA, Striano P, Nobile C.
    Neurology; 2012 Apr 24; 78(17):1299-303. PubMed ID: 22496201
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  • 31. Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins.
    Diani E, Di Bonaventura C, Mecarelli O, Gambardella A, Elia M, Bovo G, Bisulli F, Pinardi F, Binelli S, Egeo G, Castellotti B, Striano P, Striano S, Bianchi A, Ferlazzo E, Vianello V, Coppola G, Aguglia U, Tinuper P, Giallonardo AT, Michelucci R, Nobile C.
    Epilepsy Res; 2008 Jul 24; 80(1):1-8. PubMed ID: 18440780
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  • 33. LGI1 mutations in autosomal dominant partial epilepsy with auditory features.
    Ottman R, Winawer MR, Kalachikov S, Barker-Cummings C, Gilliam TC, Pedley TA, Hauser WA.
    Neurology; 2004 Apr 13; 62(7):1120-6. PubMed ID: 15079011
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  • 37. A rat model for LGI1-related epilepsies.
    Baulac S, Ishida S, Mashimo T, Boillot M, Fumoto N, Kuwamura M, Ohno Y, Takizawa A, Aoto T, Ueda M, Ikeda A, LeGuern E, Takahashi R, Serikawa T.
    Hum Mol Genet; 2012 Aug 15; 21(16):3546-57. PubMed ID: 22589250
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  • 39. The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations.
    Michelucci R, Pulitano P, Di Bonaventura C, Binelli S, Luisi C, Pasini E, Striano S, Striano P, Coppola G, La Neve A, Giallonardo AT, Mecarelli O, Serioli E, Dazzo E, Fanciulli M, Nobile C.
    Epilepsy Behav; 2017 Mar 15; 68():103-107. PubMed ID: 28142128
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  • 40. Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia.
    Klein KM, Pendziwiat M, Cohen R, Appenzeller S, de Kovel CG, Rosenow F, Koeleman BP, Kuhlenbäumer G, Sheintuch L, Veksler R, Friedman A, Afawi Z, Helbig I.
    J Neurol; 2016 Jan 15; 263(1):11-6. PubMed ID: 26459092
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