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Journal Abstract Search

163 related items for PubMed ID: 23651915

  • 1. Hyperactive behavior in a family with autosomal dominant lateral temporal lobe epilepsy caused by a mutation in the LGI1/epitempin gene.
    Berghuis B, Brilstra EH, Lindhout D, Baulac S, de Haan GJ, van Kempen M.
    Epilepsy Behav; 2013 Jul; 28(1):41-6. PubMed ID: 23651915
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  • 2. Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.
    Michelucci R, Pasini E, Malacrida S, Striano P, Bonaventura CD, Pulitano P, Bisulli F, Egeo G, Santulli L, Sofia V, Gambardella A, Elia M, de Falco A, Neve Al, Banfi P, Coppola G, Avoni P, Binelli S, Boniver C, Pisano T, Marchini M, Dazzo E, Fanciulli M, Bartolini Y, Riguzzi P, Volpi L, de Falco FA, Giallonardo AT, Mecarelli O, Striano S, Tinuper P, Nobile C.
    Epilepsia; 2013 Jul; 54(7):1288-97. PubMed ID: 23621105
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  • 4. LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures.
    Gu W, Brodtkorb E, Steinlein OK.
    Ann Neurol; 2002 Sep; 52(3):364-7. PubMed ID: 12205652
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  • 5. Autosomal dominant lateral temporal epilepsy (ADLTE): novel structural and single-nucleotide LGI1 mutations in families with predominant visual auras.
    Dazzo E, Santulli L, Posar A, Fattouch J, Conti S, Lodén-van Straaten M, Mijalkovic J, De Bortoli M, Rosa M, Millino C, Pacchioni B, Di Bonaventura C, Giallonardo AT, Striano S, Striano P, Parmeggiani A, Nobile C.
    Epilepsy Res; 2015 Feb; 110():132-8. PubMed ID: 25616465
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  • 7. Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy.
    Chabrol E, Gourfinkel-An I, Scheffer IE, Picard F, Couarch P, Berkovic SF, McMahon JM, Bajaj N, Mota-Vieira L, Mota R, Trouillard O, Depienne C, Baulac M, LeGuern E, Baulac S.
    Epilepsy Res; 2007 Aug; 76(1):41-8. PubMed ID: 17681454
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  • 8. [Clinical characteristics and LGI1 gene mutation analysis on an autosomal dominant lateral temporal lobe epilepsy].
    Xi ZQ, Wang XF, Lü Y, Wang L, Xiao F, Guan LF.
    Zhonghua Yi Xue Za Zhi; 2009 Jan 20; 89(3):195-7. PubMed ID: 19537038
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  • 9. 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 20; 45(3):218-22. PubMed ID: 15009222
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  • 10. 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 20; 120():73-8. PubMed ID: 26773249
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  • 11. A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy.
    Striano P, de Falco A, Diani E, Bovo G, Furlan S, Vitiello L, Pinardi F, Striano S, Michelucci R, de Falco FA, Nobile C.
    Arch Neurol; 2008 Jul 20; 65(7):939-42. PubMed ID: 18625862
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  • 13. Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy.
    Bovo G, Diani E, Bisulli F, Di Bonaventura C, Striano P, Gambardella A, Ferlazzo E, Egeo G, Mecarelli O, Elia M, Bianchi A, Bortoluzzi S, Vettori A, Aguglia U, Binelli S, De Falco A, Coppola G, Gobbi G, Sofia V, Striano S, Tinuper P, Giallonardo AT, Michelucci R, Nobile C.
    Neurosci Lett; 2008 May 02; 436(1):23-6. PubMed ID: 18355961
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  • 14. Two novel epilepsy-linked mutations leading to a loss of function of LGI1.
    Chabrol E, Popescu C, Gourfinkel-An I, Trouillard O, Depienne C, Senechal K, Baulac M, LeGuern E, Baulac S.
    Arch Neurol; 2007 Feb 02; 64(2):217-22. PubMed ID: 17296837
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  • 16. Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families.
    Michelucci R, Poza JJ, Sofia V, de Feo MR, Binelli S, Bisulli F, Scudellaro E, Simionati B, Zimbello R, D'Orsi G, Passarelli D, Avoni P, Avanzini G, Tinuper P, Biondi R, Valle G, Mautner VF, Stephani U, Tassinari CA, Moschonas NK, Siebert R, Lopez de Munain A, Perez-Tur J, Nobile C.
    Epilepsia; 2003 Oct 02; 44(10):1289-97. PubMed ID: 14510822
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  • 17. 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 02; 50(11):2481-6. PubMed ID: 19552651
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  • 18. Mutation analysis of the leucine-rich, glioma inactivated 1 gene (LGI1) in Japanese febrile seizure patients.
    Nakayama J, Hamano K, Iwasaki N, Ohta M, Nakahara S, Matsui A, Arinami T.
    Neuropediatrics; 2003 Jun 02; 34(5):234-6. PubMed ID: 14598228
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