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 *

136 related articles for article (PubMed ID: 17562837)

  • 1. A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures.
    Michelucci R; Mecarelli O; Bovo G; Bisulli F; Testoni S; Striano P; Striano S; Tinuper P; Nobile C
    Neurology; 2007 Jun; 68(24):2150-1. PubMed ID: 17562837
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Re: CDKL5 mutations in boys with severe encephalopathy and early-onset intractable epilepsy.
    Fichou Y; Bieth E; Bahi-Buisson N; Nectoux J; Girard B; Chelly J; Chaix Y; Bienvenu T
    Neurology; 2009 Jul; 73(1):77-8; author reply 78. PubMed ID: 19564592
    [No Abstract]   [Full Text] [Related]  

  • 4. Neurological findings in aminoacylase 1 deficiency.
    Sass JO; Olbrich H; Mohr V; Hart C; Woldseth B; Krywawych S; Bjurulf B; Lakhani PK; Buchdahl RM; Omran H
    Neurology; 2007 Jun; 68(24):2151-3. PubMed ID: 17562838
    [No Abstract]   [Full Text] [Related]  

  • 5. Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice.
    Chabrol E; Navarro V; Provenzano G; Cohen I; Dinocourt C; Rivaud-PĂ©choux S; Fricker D; Baulac M; Miles R; Leguern E; Baulac S
    Brain; 2010 Sep; 133(9):2749-62. PubMed ID: 20659958
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Kv4.2 truncation mutation in a patient with temporal lobe epilepsy.
    Singh B; Ogiwara I; Kaneda M; Tokonami N; Mazaki E; Baba K; Matsuda K; Inoue Y; Yamakawa K
    Neurobiol Dis; 2006 Nov; 24(2):245-53. PubMed ID: 16934482
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Structural anomaly of left lateral temporal lobe in epilepsy due to mutated LGI1.
    Tessa C; Michelucci R; Nobile C; Giannelli M; Della Nave R; Testoni S; Bianucci D; Tinuper P; Bisulli F; Sofia V; De Feo MR; Giallonardo AT; Tassinari CA; Mascalchi M
    Neurology; 2007 Sep; 69(12):1298-300. PubMed ID: 17875918
    [No Abstract]   [Full Text] [Related]  

  • 8. Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy.
    D'Agostino D; Bertelli M; Gallo S; Cecchin S; Albiero E; Garofalo PG; Gambardella A; St Hilaire JM; Kwiecinski H; Andermann E; Pandolfo M
    Neurology; 2004 Oct; 63(8):1500-2. PubMed ID: 15505175
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Late-onset childhood occipital epilepsy (Gastaut type): a family study.
    Grosso S; Vivarelli R; Gobbi G; Di Bartolo R; Berardi R; Balestri P
    Eur J Paediatr Neurol; 2008 Sep; 12(5):421-6. PubMed ID: 18249143
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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; 107(3):311-7. PubMed ID: 24206907
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel inherited mutation in the voltage sensor region of SCN1A is associated with Panayiotopoulos syndrome in siblings and generalized epilepsy with febrile seizures plus.
    Livingston JH; Cross JH; Mclellan A; Birch R; Zuberi SM
    J Child Neurol; 2009 Apr; 24(4):503-8. PubMed ID: 19339291
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Genetics of the epilepsies.
    Gutierrez-Delicado E; Serratosa JM
    Curr Opin Neurol; 2004 Apr; 17(2):147-53. PubMed ID: 15021241
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Speech-induced aphasic seizures in epilepsy caused by LGI1 mutation.
    Brodtkorb E; Michler RP; Gu W; Steinlein OK
    Epilepsia; 2005 Jun; 46(6):963-6. PubMed ID: 15946341
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism.
    Bernardi L; Tomaino C; Anfossi M; Gallo M; Geracitano S; Puccio G; Colao R; Frangipane F; Mirabelli M; Smirne N; Maletta RG; Bruni AC
    J Neurol; 2008 Apr; 255(4):604-6. PubMed ID: 18350357
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsy.
    Holland KD; Kearney JA; Glauser TA; Buck G; Keddache M; Blankston JR; Glaaser IW; Kass RS; Meisler MH
    Neurosci Lett; 2008 Mar; 433(1):65-70. PubMed ID: 18242854
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.