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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

164 related items for PubMed ID: 15009222

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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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  • 3. 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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  • 4. 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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  • 5. Mutations in LGI1 gene in Japanese families with autosomal dominant lateral temporal lobe epilepsy: the first report from Asian families.
    Kawamata J, Ikeda A, Fujita Y, Usui K, Shimohama S, Takahashi R.
    Epilepsia; 2010 Apr; 51(4):690-3. PubMed ID: 19780791
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  • 6. 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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  • 11. 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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  • 12. 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 13; 44(10):1289-97. PubMed ID: 14510822
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  • 14. 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 13; 263(1):11-6. PubMed ID: 26459092
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  • 16. 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 13; 107(3):311-7. PubMed ID: 24206907
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  • 20. LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures.
    Gu W, Brodtkorb E, Steinlein OK.
    Ann Neurol; 2002 Sep 13; 52(3):364-7. PubMed ID: 12205652
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