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 *

261 related articles for article (PubMed ID: 22050316)

  • 1. Dravet syndrome--considerable delay in making the diagnosis.
    Bremer A; Lossius MI; Nakken KO
    Acta Neurol Scand; 2012 May; 125(5):359-62. PubMed ID: 22050316
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Atypical multifocal Dravet syndrome lacks generalized seizures and may show later cognitive decline.
    Kim YO; Bellows S; McMahon JM; Iona X; Damiano J; Dibbens L; Kelley K; Gill D; Cross JH; Berkovic SF; Scheffer IE
    Dev Med Child Neurol; 2014 Jan; 56(1):85-90. PubMed ID: 24328833
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutations.
    Xu X; Zhang Y; Sun H; Liu X; Yang X; Xiong H; Jiang Y; Bao X; Wang S; Yang Z; Wu Y; Qin J; Lin Q; Wu X
    Brain Dev; 2014 Sep; 36(8):676-81. PubMed ID: 24168886
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Diagnosis and long-term course of Dravet syndrome.
    Scheffer IE
    Eur J Paediatr Neurol; 2012 Sep; 16 Suppl 1():S5-8. PubMed ID: 22704920
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patients.
    Ragona F; Brazzo D; De Giorgi I; Morbi M; Freri E; Teutonico F; Gennaro E; Zara F; Binelli S; Veggiotti P; Granata T
    Brain Dev; 2010 Jan; 32(1):71-7. PubMed ID: 19854600
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?
    Lim BC; Hwang H; Kim H; Chae JH; Choi J; Kim KJ; Hwang YS; Yum MS; Ko TS
    Epilepsy Res; 2015 Jan; 109():34-9. PubMed ID: 25524840
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Dravet syndrome: the main issues.
    Guerrini R
    Eur J Paediatr Neurol; 2012 Sep; 16 Suppl 1():S1-4. PubMed ID: 22705271
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Defining Dravet syndrome: An essential pre-requisite for precision medicine trials.
    Li W; Schneider AL; Scheffer IE
    Epilepsia; 2021 Sep; 62(9):2205-2217. PubMed ID: 34338318
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical and genetic factors predicting Dravet syndrome in infants with
    Cetica V; Chiari S; Mei D; Parrini E; Grisotto L; Marini C; Pucatti D; Ferrari A; Sicca F; Specchio N; Trivisano M; Battaglia D; Contaldo I; Zamponi N; Petrelli C; Granata T; Ragona F; Avanzini G; Guerrini R
    Neurology; 2017 Mar; 88(11):1037-1044. PubMed ID: 28202706
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations.
    Carranza Rojo D; Harvey AS; Iona X; Dibbens LM; Damiano JA; Arsov T; Gill D; Freeman JL; Leventer RJ; Vincent A; Berkovic SF; McMahon JM; Scheffer IE
    Epilepsy Res; 2012 Jun; 100(1-2):194-8. PubMed ID: 22386634
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The incidence of SCN1A-related Dravet syndrome in Denmark is 1:22,000: a population-based study from 2004 to 2009.
    Bayat A; Hjalgrim H; Møller RS
    Epilepsia; 2015 Apr; 56(4):e36-9. PubMed ID: 25778844
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Adults with a history of possible Dravet syndrome: an illustration of the importance of analysis of the SCN1A gene.
    Verbeek NE; van Kempen M; Gunning WB; Renier WO; Westland B; Lindhout D; Brilstra EH
    Epilepsia; 2011 Apr; 52(4):e23-5. PubMed ID: 21371021
    [TBL] [Abstract][Full Text] [Related]  

  • 16. When is a child with status epilepticus likely to have Dravet syndrome?
    Le Gal F; Lebon S; Ramelli GP; Datta AN; Mercati D; Maier O; Combescure C; Rodriguez MI; Seeck M; Roulet E; Korff CM
    Epilepsy Res; 2014 May; 108(4):740-7. PubMed ID: 24679980
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Severe myoclonic epilepsy of infancy (Dravet syndrome): recognition and diagnosis in adults.
    Jansen FE; Sadleir LG; Harkin LA; Vadlamudi L; McMahon JM; Mulley JC; Scheffer IE; Berkovic SF
    Neurology; 2006 Dec; 67(12):2224-6. PubMed ID: 17190949
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Dravet syndrome as a cause of epilepsy and learning disability].
    Lund C; Bremer A; Lossius MI; Selmer KK; Brodtkorb E; Nakken KO
    Tidsskr Nor Laegeforen; 2012 Jan; 132(1):44-7. PubMed ID: 22240828
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The European patient with Dravet syndrome: results from a parent-reported survey on antiepileptic drug use in the European population with Dravet syndrome.
    Aras LM; Isla J; Mingorance-Le Meur A
    Epilepsy Behav; 2015 Mar; 44():104-9. PubMed ID: 25666511
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Influence of contraindicated medication use on cognitive outcome in Dravet syndrome and age at first afebrile seizure as a clinical predictor in SCN1A-related seizure phenotypes.
    de Lange IM; Gunning B; Sonsma ACM; van Gemert L; van Kempen M; Verbeek NE; Nicolai J; Knoers NVAM; Koeleman BPC; Brilstra EH
    Epilepsia; 2018 Jun; 59(6):1154-1165. PubMed ID: 29750338
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.