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 *

326 related articles for article (PubMed ID: 15021241)

  • 1. 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]  

  • 2. Channelopathies as a genetic cause of epilepsy.
    Mulley JC; Scheffer IE; Petrou S; Berkovic SF
    Curr Opin Neurol; 2003 Apr; 16(2):171-6. PubMed ID: 12644745
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Expansion of the first polyalanine tract of the ARX gene in a boy presenting with generalized dystonia in the absence of infantile spasms.
    Shinozaki Y; Osawa M; Sakuma H; Komaki H; Nakagawa E; Sugai K; Sasaki M; Goto Y
    Brain Dev; 2009 Jun; 31(6):469-72. PubMed ID: 18823727
    [TBL] [Abstract][Full Text] [Related]  

  • 4. New insights into the molecular and genetic mechanisms underlying idiopathic epilepsies.
    Steinlein OK
    Clin Genet; 1998 Sep; 54(3):169-75. PubMed ID: 9788717
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The three stages of epilepsy in patients with CDKL5 mutations.
    Bahi-Buisson N; Kaminska A; Boddaert N; Rio M; Afenjar A; Gérard M; Giuliano F; Motte J; Héron D; Morel MA; Plouin P; Richelme C; des Portes V; Dulac O; Philippe C; Chiron C; Nabbout R; Bienvenu T
    Epilepsia; 2008 Jun; 49(6):1027-37. PubMed ID: 18266744
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The ARX story (epilepsy, mental retardation, autism, and cerebral malformations): one gene leads to many phenotypes.
    Sherr EH
    Curr Opin Pediatr; 2003 Dec; 15(6):567-71. PubMed ID: 14631200
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pathophysiology of epilepsy.
    Engelborghs S; D'Hooge R; De Deyn PP
    Acta Neurol Belg; 2000 Dec; 100(4):201-13. PubMed ID: 11233674
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Targeted loss of Arx results in a developmental epilepsy mouse model and recapitulates the human phenotype in heterozygous females.
    Marsh E; Fulp C; Gomez E; Nasrallah I; Minarcik J; Sudi J; Christian SL; Mancini G; Labosky P; Dobyns W; Brooks-Kayal A; Golden JA
    Brain; 2009 Jun; 132(Pt 6):1563-76. PubMed ID: 19439424
    [TBL] [Abstract][Full Text] [Related]  

  • 9. X-linked mental retardation and epilepsy: pathogenetic significance of ARX mutations.
    Hirose S; Mitsudome A
    Brain Dev; 2003 Apr; 25(3):161-5. PubMed ID: 12689693
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genes associated with idiopathic epilepsies: a current overview.
    Lu Y; Wang X
    Neurol Res; 2009 Mar; 31(2):135-43. PubMed ID: 19298753
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetics of the epilepsies.
    Elmslie F; Gardiner M
    Curr Opin Neurol; 1995 Apr; 8(2):126-9. PubMed ID: 7620586
    [TBL] [Abstract][Full Text] [Related]  

  • 12. CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancy.
    Nabbout R; Depienne C; Chipaux M; Girard B; Souville I; Trouillard O; Dulac O; Chelly J; Afenjar A; Héron D; Leguern E; Beldjord C; Bienvenu T; Bahi-Buisson N
    Epilepsy Res; 2009 Nov; 87(1):25-30. PubMed ID: 19734009
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Expansion of the first PolyA tract of ARX causes infantile spasms and status dystonicus.
    Guerrini R; Moro F; Kato M; Barkovich AJ; Shiihara T; McShane MA; Hurst J; Loi M; Tohyama J; Norci V; Hayasaka K; Kang UJ; Das S; Dobyns WB
    Neurology; 2007 Jul; 69(5):427-33. PubMed ID: 17664401
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sacred disease secrets revealed: the genetics of human epilepsy.
    Turnbull J; Lohi H; Kearney JA; Rouleau GA; Delgado-Escueta AV; Meisler MH; Cossette P; Minassian BA
    Hum Mol Genet; 2005 Oct; 14 Spec No. 2():2491-2500. PubMed ID: 16278970
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation screening of the Aristaless-related homeobox (ARX) gene in Thai pediatric patients with delayed development: first report from Thailand.
    Rujirabanjerd S; Tongsippunyoo K; Sripo T; Limprasert P
    Eur J Med Genet; 2007; 50(5):346-54. PubMed ID: 17613295
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Molecular genetics of intractable epilepsies].
    Kato M
    No To Hattatsu; 2014 May; 46(3):191-4. PubMed ID: 24902337
    [No Abstract]   [Full Text] [Related]  

  • 17. Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation.
    Kalscheuer VM; Tao J; Donnelly A; Hollway G; Schwinger E; Kübart S; Menzel C; Hoeltzenbein M; Tommerup N; Eyre H; Harbord M; Haan E; Sutherland GR; Ropers HH; Gécz J
    Am J Hum Genet; 2003 Jun; 72(6):1401-11. PubMed ID: 12736870
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new paradigm for West syndrome based on molecular and cell biology.
    Kato M
    Epilepsy Res; 2006 Aug; 70 Suppl 1():S87-95. PubMed ID: 16806828
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.
    Vanmolkot KR; Kors EE; Hottenga JJ; Terwindt GM; Haan J; Hoefnagels WA; Black DF; Sandkuijl LA; Frants RR; Ferrari MD; van den Maagdenberg AM
    Ann Neurol; 2003 Sep; 54(3):360-6. PubMed ID: 12953268
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetics of idiopathic epilepsies.
    Hirose S; Mitsudome A; Okada M; Kaneko S;
    Epilepsia; 2005; 46 Suppl 1():38-43. PubMed ID: 15816978
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.