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Journal Abstract Search

164 related items for PubMed ID: 15009222

  • 21. 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; 65(7):939-42. PubMed ID: 18625862
    [Abstract] [Full Text] [Related]

  • 22. 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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  • 23. Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy.
    Ayerdi-Izquierdo A, Stavrides G, Sellés-Martínez JJ, Larrea L, Bovo G, López de Munain A, Bisulli F, Martí-Massó JF, Michelucci R, Poza JJ, Tinuper P, Stephani U, Striano P, Striano S, Staub E, Sarafidou T, Hinzmann B, Moschonas N, Siebert R, Deloukas P, Nobile C, Pérez-Tur J.
    Epilepsy Res; 2006 Aug; 70(2-3):118-26. PubMed ID: 16707245
    [Abstract] [Full Text] [Related]

  • 24. 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
    [Abstract] [Full Text] [Related]

  • 25. 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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  • 26. 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; 34(5):234-6. PubMed ID: 14598228
    [Abstract] [Full Text] [Related]

  • 27. 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; 80(1):1-8. PubMed ID: 18440780
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  • 29. 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; 68():103-107. PubMed ID: 28142128
    [Abstract] [Full Text] [Related]

  • 30. Partial epilepsy with prominent auditory symptoms not linked to chromosome 10q.
    Bisulli F, Tinuper P, Marini C, Avoni P, Carraro G, Nobile C.
    Epileptic Disord; 2002 Sep; 4(3):183-7. PubMed ID: 12446220
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  • 33. 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
    [Abstract] [Full Text] [Related]

  • 34. 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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  • 37. Mutations in MICAL-1cause autosomal-dominant lateral temporal epilepsy.
    Dazzo E, Rehberg K, Michelucci R, Passarelli D, Boniver C, Vianello Dri V, Striano P, Striano S, Pasterkamp RJ, Nobile C.
    Ann Neurol; 2018 Mar; 83(3):483-493. PubMed ID: 29394500
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  • 39. Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy.
    Dazzo E, Fanciulli M, Serioli E, Minervini G, Pulitano P, Binelli S, Di Bonaventura C, Luisi C, Pasini E, Striano S, Striano P, Coppola G, Chiavegato A, Radovic S, Spadotto A, Uzzau S, La Neve A, Giallonardo AT, Mecarelli O, Tosatto SC, Ottman R, Michelucci R, Nobile C.
    Am J Hum Genet; 2015 Jun 04; 96(6):992-1000. PubMed ID: 26046367
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  • 40. Low penetrance and effect on protein secretion of LGI1 mutations causing autosomal dominant lateral temporal epilepsy.
    Di Bonaventura C, Operto FF, Busolin G, Egeo G, D'Aniello A, Vitello L, Smaniotto G, Furlan S, Diani E, Michelucci R, Giallonardo AT, Coppola G, Nobile C.
    Epilepsia; 2011 Jul 04; 52(7):1258-64. PubMed ID: 21504429
    [Abstract] [Full Text] [Related]

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