BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

159 related articles for article (PubMed ID: 20074235)

  • 1. The Epilepsy Genetic Association Database (epiGAD): analysis of 165 genetic association studies, 1996-2008.
    Tan NC; Berkovic SF
    Epilepsia; 2010 Apr; 51(4):686-9. PubMed ID: 20074235
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Monogenic epilepsies in humans: molecular mechanisms and relevance for the study of intractable epilepsy.
    Cossette P; Rouleau GA
    Adv Neurol; 2006; 97():381-8. PubMed ID: 16383149
    [No Abstract]   [Full Text] [Related]  

  • 3. Familial genetic predisposition, epilepsy localization and antecedent febrile seizures.
    Abou-Khalil B; Krei L; Lazenby B; Harris PA; Haines JL; Hedera P
    Epilepsy Res; 2007 Jan; 73(1):104-10. PubMed ID: 17046202
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genes and mutations in idiopathic epilepsy.
    Steinlein OK
    Am J Med Genet; 2001; 106(2):139-45. PubMed ID: 11579434
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic association studies in epilepsy: "the truth is out there".
    Tan NC; Mulley JC; Berkovic SF
    Epilepsia; 2004 Nov; 45(11):1429-42. PubMed ID: 15509244
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic influence on the clinical characteristics and outcome of febrile seizures--a retrospective study.
    Birca A; Guy N; Fortier I; Cossette P; Lortie A; Carmant L
    Eur J Paediatr Neurol; 2005; 9(5):339-45. PubMed ID: 15979359
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Incidence of epilepsies and epileptic syndromes among children in Navarre, Spain: 2002 through 2005.
    Durá-Travé T; Yoldi-Petri ME; Gallinas-Victoriano F
    J Child Neurol; 2008 Aug; 23(8):878-82. PubMed ID: 18660472
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identified.
    Zucca C; Redaelli F; Epifanio R; Zanotta N; Romeo A; Lodi M; Veggiotti P; Airoldi G; Panzeri C; Romaniello R; De Polo G; Bonanni P; Cardinali S; Baschirotto C; Martorell L; Borgatti R; Bresolin N; Bassi MT
    Arch Neurol; 2008 Apr; 65(4):489-94. PubMed ID: 18413471
    [TBL] [Abstract][Full Text] [Related]  

  • 10. GEFS+ where focal seizures evolve from generalized spike wave: video-EEG study of two children.
    Deng YH; Berkovic SF; Scheffer IE
    Epileptic Disord; 2007 Sep; 9(3):307-14. PubMed ID: 17884755
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Monogenic idiopathic epilepsies.
    Gourfinkel-An I; Baulac S; Nabbout R; Ruberg M; Baulac M; Brice A; LeGuern E
    Lancet Neurol; 2004 Apr; 3(4):209-18. PubMed ID: 15039033
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizures.
    Doose H; Lunau H; Castiglione E; Waltz S
    Neuropediatrics; 1998 Oct; 29(5):229-38. PubMed ID: 9810557
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The Hitchhiker's guide to the child neurologist's genetic evaluation of epilepsy.
    Grill MF; Losey TE; Ng YT
    Semin Pediatr Neurol; 2008 Mar; 15(1):32-40. PubMed ID: 18342259
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Clinical investigation of genetic contributions to childhood-onset epilepsies and epileptic syndromes.
    Wakamoto H; Hayashi M; Nagao H; Morimoto T; Kida K
    Brain Dev; 2004 Apr; 26(3):184-9. PubMed ID: 15030907
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Epilepsy and genetics].
    Picard F
    Rev Med Suisse Romande; 2003 May; 123(5):317-21. PubMed ID: 15095716
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic predisposition to severe myoclonic epilepsy in infancy.
    Benlounis A; Nabbout R; Feingold J; Parmeggiani A; Guerrini R; Kaminska A; Dulac O
    Epilepsia; 2001 Feb; 42(2):204-9. PubMed ID: 11240590
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetics of epilepsy.
    Pandolfo M
    Semin Neurol; 2011 Nov; 31(5):506-18. PubMed ID: 22266888
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel susceptibility locus at 2p24 for generalised epilepsy with febrile seizures plus.
    Audenaert D; Claes L; Claeys KG; Deprez L; Van Dyck T; Goossens D; Del-Favero J; Van Paesschen W; Van Broeckhoven C; De Jonghe P
    J Med Genet; 2005 Dec; 42(12):947-52. PubMed ID: 15827091
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Atypical "benign" partial epilepsy of childhood or pseudo-lennox syndrome. Part II: family study.
    Doose H; Hahn A; Neubauer BA; Pistohl J; Stephani U
    Neuropediatrics; 2001 Feb; 32(1):9-13. PubMed ID: 11315204
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.