BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

263 related articles for article (PubMed ID: 15079011)

  • 1. 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; 62(7):1120-6. PubMed ID: 15079011
    [TBL] [Abstract][Full Text] [Related]  

  • 2. LGI1 mutations in temporal lobe epilepsies.
    Berkovic SF; Izzillo P; McMahon JM; Harkin LA; McIntosh AM; Phillips HA; Briellmann RS; Wallace RH; Mazarib A; Neufeld MY; Korczyn AD; Scheffer IE; Mulley JC
    Neurology; 2004 Apr; 62(7):1115-9. PubMed ID: 15079010
    [TBL] [Abstract][Full Text] [Related]  

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

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. LGI1 gene mutation screening in sporadic partial epilepsy with auditory features.
    Flex E; Pizzuti A; Di Bonaventura C; Douzgou S; Egeo G; Fattouch J; Manfredi M; Dallapiccola B; Giallonardo AT
    J Neurol; 2005 Jan; 252(1):62-6. PubMed ID: 15654555
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Penetrance of LGI1 mutations in autosomal dominant partial epilepsy with auditory features.
    Rosanoff MJ; Ottman R
    Neurology; 2008 Aug; 71(8):567-71. PubMed ID: 18711109
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases.
    Bisulli F; Tinuper P; Avoni P; Striano P; Striano S; d'Orsi G; Vignatelli L; Bagattin A; Scudellaro E; Florindo I; Nobile C; Tassinari CA; Baruzzi A; Michelucci R
    Brain; 2004 Jun; 127(Pt 6):1343-52. PubMed ID: 15090473
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 263(1):11-6. PubMed ID: 26459092
    [TBL] [Abstract][Full Text] [Related]  

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

  • 10. Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features.
    Kalachikov S; Evgrafov O; Ross B; Winawer M; Barker-Cummings C; Martinelli Boneschi F; Choi C; Morozov P; Das K; Teplitskaya E; Yu A; Cayanis E; Penchaszadeh G; Kottmann AH; Pedley TA; Hauser WA; Ottman R; Gilliam TC
    Nat Genet; 2002 Mar; 30(3):335-41. PubMed ID: 11810107
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 45(3):218-22. PubMed ID: 15009222
    [TBL] [Abstract][Full Text] [Related]  

  • 12. ADPEAF mutations reduce levels of secreted LGI1, a putative tumor suppressor protein linked to epilepsy.
    Senechal KR; Thaller C; Noebels JL
    Hum Mol Genet; 2005 Jun; 14(12):1613-20. PubMed ID: 15857855
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24.
    Winawer MR; Martinelli Boneschi F; Barker-Cummings C; Lee JH; Liu J; Mekios C; Gilliam TC; Pedley TA; Hauser WA; Ottman R
    Epilepsia; 2002 Jan; 43(1):60-7. PubMed ID: 11879388
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel LGI1 mutation in a family with autosomal dominant partial epilepsy with auditory features.
    Fertig E; Lincoln A; Martinuzzi A; Mattson RH; Hisama FM
    Neurology; 2003 May; 60(10):1687-90. PubMed ID: 12771268
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Altered language processing in autosomal dominant partial epilepsy with auditory features.
    Ottman R; Rosenberger L; Bagic A; Kamberakis K; Ritzl EK; Wohlschlager AM; Shamim S; Sato S; Liew C; Gaillard WD; Wiggs E; Berl MM; Reeves-Tyer P; Baker EH; Butman JA; Theodore WH
    Neurology; 2008 Dec; 71(24):1973-80. PubMed ID: 19064878
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Domain-dependent clustering and genotype-phenotype analysis of LGI1 mutations in ADPEAF.
    Ho YY; Ionita-Laza I; Ottman R
    Neurology; 2012 Feb; 78(8):563-8. PubMed ID: 22323750
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.