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PUBMED FOR HANDHELDS

Journal Abstract Search


152 related items for PubMed ID: 29034879

  • 1. 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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  • 4. LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy.
    Nobile C, Michelucci R, Andreazza S, Pasini E, Tosatto SC, Striano P.
    Hum Mutat; 2009 Apr; 30(4):530-6. PubMed ID: 19191227
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  • 6. 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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  • 7. Autosomal dominant lateral temporal epilepsy (ADLTE): absence of chromosomal rearrangements in LGI1 gene.
    Manna I, Mumoli L, Labate A, Citrigno L, Ferlazzo E, Aguglia U, Quattrone A, Gambardella A.
    Epilepsy Res; 2014 Mar; 108(3):597-9. PubMed ID: 24315022
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  • 12. 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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  • 13. 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; 120():73-8. PubMed ID: 26773249
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  • 14. 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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  • 15. 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 02; 45(3):218-22. PubMed ID: 15009222
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  • 20. Arrested maturation of excitatory synapses in autosomal dominant lateral temporal lobe epilepsy.
    Zhou YD, Lee S, Jin Z, Wright M, Smith SE, Anderson MP.
    Nat Med; 2009 Oct 02; 15(10):1208-14. PubMed ID: 19701204
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