BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

379 related articles for article (PubMed ID: 21248271)

  • 21. Therapy for hyperthermia-induced seizures in Scn1a mutant rats.
    Hayashi K; Ueshima S; Ouchida M; Mashimo T; Nishiki T; Sendo T; Serikawa T; Matsui H; Ohmori I
    Epilepsia; 2011 May; 52(5):1010-7. PubMed ID: 21480876
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an SCN1A mutation.
    Hindocha N; Nashef L; Elmslie F; Birch R; Zuberi S; Al-Chalabi A; Crotti L; Schwartz PJ; Makoff A
    Epilepsia; 2008 Feb; 49(2):360-5. PubMed ID: 18251839
    [No Abstract]   [Full Text] [Related]  

  • 23. Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.
    Marini C; Mei D; Temudo T; Ferrari AR; Buti D; Dravet C; Dias AI; Moreira A; Calado E; Seri S; Neville B; Narbona J; Reid E; Michelucci R; Sicca F; Cross HJ; Guerrini R
    Epilepsia; 2007 Sep; 48(9):1678-1685. PubMed ID: 17561957
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus.
    Hawkins NA; Martin MS; Frankel WN; Kearney JA; Escayg A
    Neurobiol Dis; 2011 Mar; 41(3):655-60. PubMed ID: 21156207
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Phenotypes and genotypes in epilepsy with febrile seizures plus.
    Ito M; Yamakawa K; Sugawara T; Hirose S; Fukuma G; Kaneko S
    Epilepsy Res; 2006 Aug; 70 Suppl 1():S199-205. PubMed ID: 16884893
    [TBL] [Abstract][Full Text] [Related]  

  • 26. SCN1A variant in a Scandinavian GEFS+ family: a wolf in sheep's clothing?
    Holland KD
    Acta Neurol Scand; 2008 Nov; 118(5):344-5; author reply 346. PubMed ID: 18616623
    [No Abstract]   [Full Text] [Related]  

  • 27. Neonatal epilepsy syndromes and GEFS+: mechanistic considerations.
    Burgess DL
    Epilepsia; 2005; 46 Suppl 10():51-8. PubMed ID: 16359473
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Clinical spectrum of mutations in SCN1A gene: severe myoclonic epilepsy in infancy and related epilepsies.
    Fujiwara T
    Epilepsy Res; 2006 Aug; 70 Suppl 1():S223-30. PubMed ID: 16806826
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Gene symbol: SCN1A. Disease: Generalized epilepsy with febrile seizures plus.
    Sun H; Zhang Y; Liang J; Liu X; Ma X; Wu H; Xu K; Qin J; Qi Y; Wu X
    Hum Genet; 2008 Oct; 124(3):298. PubMed ID: 18846618
    [No Abstract]   [Full Text] [Related]  

  • 30. The spectrum of SCN1A-related infantile epileptic encephalopathies.
    Harkin LA; McMahon JM; Iona X; Dibbens L; Pelekanos JT; Zuberi SM; Sadleir LG; Andermann E; Gill D; Farrell K; Connolly M; Stanley T; Harbord M; Andermann F; Wang J; Batish SD; Jones JG; Seltzer WK; Gardner A; ; Sutherland G; Berkovic SF; Mulley JC; Scheffer IE
    Brain; 2007 Mar; 130(Pt 3):843-52. PubMed ID: 17347258
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genes and loci involved in febrile seizures and related epilepsy syndromes.
    Audenaert D; Van Broeckhoven C; De Jonghe P
    Hum Mutat; 2006 May; 27(5):391-401. PubMed ID: 16550559
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genetic screening of Scandinavian families with febrile seizures and epilepsy or GEFS+.
    Selmer KK; Egeland T; Solaas MH; Nakken KO; Kjeldsen MJ; Friis ML; Brandal K; Corey LA; Undlien DE
    Acta Neurol Scand; 2008 Apr; 117(4):289-92. PubMed ID: 17927801
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Phenotype and SCN1A gene mutation screening in 39 families with generalized epilepsy with febrile seizures plus].
    Xu XJ; Zhang YH; Sun HH; Liu XY; Wu HS; Wu XR
    Zhonghua Er Ke Za Zhi; 2012 Aug; 50(8):580-6. PubMed ID: 23158734
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus.
    Annesi G; Gambardella A; Carrideo S; Incorpora G; Labate A; Pasqua AA; Civitelli D; Polizzi A; Annesi F; Spadafora P; Tarantino P; Cirò Candiano IC; Romeo N; De Marco EV; Ventura P; LePiane E; Zappia M; Aguglia U; Pavone L; Quattrone A
    Epilepsia; 2003 Sep; 44(9):1257-8. PubMed ID: 12919402
    [No Abstract]   [Full Text] [Related]  

  • 35. Neonatal epilepsy syndromes and generalized epilepsy with febrile seizures plus (GEFS+).
    Scheffer IE; Harkin LA; Dibbens LM; Mulley JC; Berkovic SF
    Epilepsia; 2005; 46 Suppl 10():41-7. PubMed ID: 16359471
    [No Abstract]   [Full Text] [Related]  

  • 36. Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.
    Escayg A; MacDonald BT; Meisler MH; Baulac S; Huberfeld G; An-Gourfinkel I; Brice A; LeGuern E; Moulard B; Chaigne D; Buresi C; Malafosse A
    Nat Genet; 2000 Apr; 24(4):343-5. PubMed ID: 10742094
    [No Abstract]   [Full Text] [Related]  

  • 37. 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]  

  • 38. Mosaicism of a missense SCN1A mutation and Dravet syndrome in a Roma/Gypsy family.
    Azmanov DN; Zhelyazkova S; Dimova PS; Radionova M; Bojinova V; Florez L; Smith SJ; Tournev I; Jablensky A; Mulley J; Scheffer I; Kalaydjieva L; Sander JW
    Epileptic Disord; 2010 Jun; 12(2):117-24. PubMed ID: 20562086
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A novel SCN1A mutation associated with severe GEFS+ in a large South American pedigree.
    Pineda-Trujillo N; Carrizosa J; Cornejo W; Arias W; Franco C; Cabrera D; Bedoya G; Ruíz-Linares A
    Seizure; 2005 Mar; 14(2):123-8. PubMed ID: 15694566
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A screening test for the prediction of Dravet syndrome before one year of age.
    Hattori J; Ouchida M; Ono J; Miyake S; Maniwa S; Mimaki N; Ohtsuka Y; Ohmori I
    Epilepsia; 2008 Apr; 49(4):626-33. PubMed ID: 18076640
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.