BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

192 related articles for article (PubMed ID: 15079010)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

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

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. Similarity of molecular phenotype between known epilepsy gene LGI1 and disease candidate gene LGI2.
    Limviphuvadh V; Chua LL; Rahim RA; Eisenhaber F; Maurer-Stroh S; Adhikari S
    BMC Biochem; 2010 Sep; 11():39. PubMed ID: 20863412
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 76(13):1173-6. PubMed ID: 21444903
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new locus for familial temporal lobe epilepsy on chromosome 3q.
    Chahine L; Abou-Khalil B; Siren A; Andermann F; Hedera P; Ge Q; Andermann E; Pandolfo M
    Epilepsy Res; 2013 Oct; 106(3):338-44. PubMed ID: 24021842
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

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

  • 20. 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]  

    [Next]    [New Search]
    of 10.