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Journal Abstract Search

223 related items for PubMed ID: 25616465

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 5. Copy number variations and susceptibility to lateral temporal epilepsy: a study of 21 pedigrees.
    Fanciulli M, Pasini E, Malacrida S, Striano P, Striano S, Michelucci R, Ottman R, Nobile C.
    Epilepsia; 2014 Oct; 55(10):1651-8. PubMed ID: 25243798
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation.
    Striano P, Busolin G, Santulli L, Leonardi E, Coppola A, Vitiello L, Rigon L, Michelucci R, Tosatto SC, Striano S, Nobile C.
    Neurology; 2011 Mar 29; 76(13):1173-6. PubMed ID: 21444903
    [Abstract] [Full Text] [Related]

  • 8. 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 29; 45(3):218-22. PubMed ID: 15009222
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. 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 24; 68():103-107. PubMed ID: 28142128
    [Abstract] [Full Text] [Related]

  • 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 24; 44(10):1289-97. PubMed ID: 14510822
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 14. 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 02; 28(1):41-6. PubMed ID: 23651915
    [Abstract] [Full Text] [Related]

  • 15. Lateral temporal lobe epilepsies: clinical and genetic features.
    Michelucci R, Pasini E, Nobile C.
    Epilepsia; 2009 May 02; 50 Suppl 5():52-4. PubMed ID: 19469848
    [Abstract] [Full Text] [Related]

  • 16. CNTNAP2 mutations and autosomal dominant epilepsy with auditory features.
    Leonardi E, Dazzo E, Aspromonte MC, Tabaro F, Pascarelli S, Tosatto SCE, Michelucci R, Murgia A, Nobile C.
    Epilepsy Res; 2018 Jan 02; 139():51-53. PubMed ID: 29179159
    [Abstract] [Full Text] [Related]

  • 17. [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
    [Abstract] [Full Text] [Related]

  • 18. 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 20; 107(3):311-7. PubMed ID: 24206907
    [Abstract] [Full Text] [Related]

  • 19. LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures.
    Gu W, Brodtkorb E, Steinlein OK.
    Ann Neurol; 2002 Sep 20; 52(3):364-7. PubMed ID: 12205652
    [Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]

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