BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

266 related articles for article (PubMed ID: 21219303)

  • 1. A retrospective study of the relation between vaccination and occurrence of seizures in Dravet syndrome.
    Tro-Baumann B; von Spiczak S; Lotte J; Bast T; Haberlandt E; Sassen R; Freund A; Leiz S; Stephani U; Boor R; Holthausen H; Helbig I; Kluger G
    Epilepsia; 2011 Jan; 52(1):175-8. PubMed ID: 21219303
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective study.
    McIntosh AM; McMahon J; Dibbens LM; Iona X; Mulley JC; Scheffer IE; Berkovic SF
    Lancet Neurol; 2010 Jun; 9(6):592-8. PubMed ID: 20447868
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Alleged cases of vaccine encephalopathy rediagnosed years later as Dravet syndrome.
    Reyes IS; Hsieh DT; Laux LC; Wilfong AA
    Pediatrics; 2011 Sep; 128(3):e699-702. PubMed ID: 21844054
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prevalence and Characteristics of Vaccination Triggered Seizures in Dravet Syndrome in Hong Kong: A Retrospective Study.
    Wong PT; Wong VC
    Pediatr Neurol; 2016 May; 58():41-7. PubMed ID: 26995069
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome.
    Brunklaus A; Ellis R; Reavey E; Forbes GH; Zuberi SM
    Brain; 2012 Aug; 135(Pt 8):2329-36. PubMed ID: 22719002
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Effect of vaccinations on seizure risk and disease course in Dravet syndrome.
    Verbeek NE; van der Maas NA; Sonsma AC; Ippel E; Vermeer-de Bondt PE; Hagebeuk E; Jansen FE; Geesink HH; Braun KP; de Louw A; Augustijn PB; Neuteboom RF; Schieving JH; Stroink H; Vermeulen RJ; Nicolai J; Brouwer OF; van Kempen M; de Kovel CG; Kemmeren JM; Koeleman BP; Knoers NV; Lindhout D; Gunning WB; Brilstra EH
    Neurology; 2015 Aug; 85(7):596-603. PubMed ID: 26203087
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Vaccination and occurrence of seizures in SCN1A mutation-positive patients: a multicenter Italian study.
    Zamponi N; Passamonti C; Petrelli C; Veggiotti P; Baldassari C; Verrotti A; Capovilla G; Viri M; Coppola G; Vignoli A
    Pediatr Neurol; 2014 Mar; 50(3):228-32. PubMed ID: 24405698
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Dravet syndrome: seizure control and gait in adults with different SCN1A mutations.
    Rilstone JJ; Coelho FM; Minassian BA; Andrade DM
    Epilepsia; 2012 Aug; 53(8):1421-8. PubMed ID: 22780858
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Acute encephalopathy in a patient with Dravet syndrome.
    Tsuji M; Mazaki E; Ogiwara I; Wada T; Iai M; Okumura A; Yamashita S; Yamakawa K; Osaka H
    Neuropediatrics; 2011 Feb; 42(2):78-81. PubMed ID: 21647847
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The genetics of Dravet syndrome.
    Marini C; Scheffer IE; Nabbout R; Suls A; De Jonghe P; Zara F; Guerrini R
    Epilepsia; 2011 Apr; 52 Suppl 2():24-9. PubMed ID: 21463275
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Clinical and genetic diagnosis of Dravet syndrome: report of 20 cases].
    Siegler Z; Neuwirth M; Hegyi M; Paraicz E; Pálmafy B; Tegzes A; Barsi P; Karcagi V; Claes L; De Jonghe P; Herczegfalvi A; Fogarasi A
    Ideggyogy Sz; 2008 Nov; 61(11-12):402-8. PubMed ID: 19070316
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Early clinical features in Dravet syndrome patients with and without SCN1A mutations.
    Petrelli C; Passamonti C; Cesaroni E; Mei D; Guerrini R; Zamponi N; Provinciali L
    Epilepsy Res; 2012 Mar; 99(1-2):21-7. PubMed ID: 22071555
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prevalence of SCN1A-related dravet syndrome among children reported with seizures following vaccination: a population-based ten-year cohort study.
    Verbeek NE; van der Maas NA; Jansen FE; van Kempen MJ; Lindhout D; Brilstra EH
    PLoS One; 2013; 8(6):e65758. PubMed ID: 23762420
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular genetics of Dravet syndrome.
    De Jonghe P
    Dev Med Child Neurol; 2011 Apr; 53 Suppl 2():7-10. PubMed ID: 21504425
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dravet syndrome: from electroclinical characteristics to molecular biology.
    Arzimanoglou A
    Epilepsia; 2009 Sep; 50 Suppl 8():3-9. PubMed ID: 19702726
    [TBL] [Abstract][Full Text] [Related]  

  • 17. De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy.
    Claes L; Ceulemans B; Audenaert D; Smets K; Löfgren A; Del-Favero J; Ala-Mello S; Basel-Vanagaite L; Plecko B; Raskin S; Thiry P; Wolf NI; Van Broeckhoven C; De Jonghe P
    Hum Mutat; 2003 Jun; 21(6):615-21. PubMed ID: 12754708
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy.
    Ceulemans BP; Claes LR; Lagae LG
    Pediatr Neurol; 2004 Apr; 30(4):236-43. PubMed ID: 15087100
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dravet syndrome and vaccination: when science prevails over speculation.
    Wiznitzer M
    Lancet Neurol; 2010 Jun; 9(6):559-61. PubMed ID: 20447869
    [No Abstract]   [Full Text] [Related]  

  • 20. SCN1A mutation screening in adult patients with Lennox-Gastaut syndrome features.
    Selmer KK; Lund C; Brandal K; Undlien DE; Brodtkorb E
    Epilepsy Behav; 2009 Nov; 16(3):555-7. PubMed ID: 19782004
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.