These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

378 related articles for article (PubMed ID: 11810107)

  • 1. 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]  

  • 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. 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. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy.
    Morante-Redolat JM; Gorostidi-Pagola A; Piquer-Sirerol S; Sáenz A; Poza JJ; Galán J; Gesk S; Sarafidou T; Mautner VF; Binelli S; Staub E; Hinzmann B; French L; Prud'homme JF; Passarelli D; Scannapieco P; Tassinari CA; Avanzini G; Martí-Massó JF; Kluwe L; Deloukas P; Moschonas NK; Michelucci R; Siebert R; Nobile C; Pérez-Tur J; López de Munain A
    Hum Mol Genet; 2002 May; 11(9):1119-28. PubMed ID: 11978770
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Epilepsy with auditory features: a LGI1 gene mutation suggests a loss-of-function mechanism.
    Pizzuti A; Flex E; Di Bonaventura C; Dottorini T; Egeo G; Manfredi M; Dallapiccola B; Giallonardo AT
    Ann Neurol; 2003 Mar; 53(3):396-9. PubMed ID: 12601709
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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; 436(1):23-6. PubMed ID: 18355961
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Autosomal dominant partial epilepsy with auditory features: a new locus on chromosome 19q13.11-q13.31.
    Bisulli F; Naldi I; Baldassari S; Magini P; Licchetta L; Castegnaro G; Fabbri M; Stipa C; Ferrari S; Seri M; Gonçalves Silva GE; Tinuper P; Pippucci T
    Epilepsia; 2014 Jun; 55(6):841-8. PubMed ID: 24579982
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Two novel epilepsy-linked mutations leading to a loss of function of LGI1.
    Chabrol E; Popescu C; Gourfinkel-An I; Trouillard O; Depienne C; Senechal K; Baulac M; LeGuern E; Baulac S
    Arch Neurol; 2007 Feb; 64(2):217-22. PubMed ID: 17296837
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. A rat model for LGI1-related epilepsies.
    Baulac S; Ishida S; Mashimo T; Boillot M; Fumoto N; Kuwamura M; Ohno Y; Takizawa A; Aoto T; Ueda M; Ikeda A; LeGuern E; Takahashi R; Serikawa T
    Hum Mol Genet; 2012 Aug; 21(16):3546-57. PubMed ID: 22589250
    [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 19.