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 *

146 related articles for article (PubMed ID: 21269283)

  • 1. Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients.
    Ragona F; Granata T; Dalla Bernardina B; Offredi F; Darra F; Battaglia D; Morbi M; Brazzo D; Cappelletti S; Chieffo D; De Giorgi I; Fontana E; Freri E; Marini C; Toraldo A; Specchio N; Veggiotti P; Vigevano F; Guerrini R; Guzzetta F; Dravet C
    Epilepsia; 2011 Feb; 52(2):386-92. PubMed ID: 21269283
    [TBL] [Abstract][Full Text] [Related]  

  • 2. An unexpected EEG course in Dravet syndrome.
    Nabbout R; Desguerre I; Sabbagh S; Depienne C; Plouin P; Dulac O; Chiron C
    Epilepsy Res; 2008 Sep; 81(1):90-5. PubMed ID: 18539001
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. Neuropsychological development in children with Dravet syndrome.
    Chieffo D; Battaglia D; Lettori D; Del Re M; Brogna C; Dravet C; Mercuri E; Guzzetta F
    Epilepsy Res; 2011 Jun; 95(1-2):86-93. PubMed ID: 21474289
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial severe myoclonic epilepsy of infancy: truncation of Nav1.1 and genetic heterogeneity.
    Gennaro E; Veggiotti P; Malacarne M; Madia F; Cecconi M; Cardinali S; Cassetti A; Cecconi I; Bertini E; Bianchi A; Gobbi G; Zara F
    Epileptic Disord; 2003 Mar; 5(1):21-5. PubMed ID: 12773292
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Low long-term efficacy and tolerability of add-on rufinamide in patients with Dravet syndrome.
    Mueller A; Boor R; Coppola G; Striano P; Dahlin M; von Stuelpnagel C; Lotte J; Staudt M; Kluger G
    Epilepsy Behav; 2011 Jul; 21(3):282-4. PubMed ID: 21620771
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Genotype-phenotype correlations in a group of 15 SCN1A-mutated Italian patients with GEFS+ spectrum (seizures plus, classical and borderline severe myoclonic epilepsy of infancy).
    Nicita F; Spalice A; Papetti L; Ursitti F; Parisi P; Gennaro E; Zara F; Iannetti P
    J Child Neurol; 2010 Nov; 25(11):1369-76. PubMed ID: 20729507
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Acute encephalopathy in children with Dravet syndrome.
    Okumura A; Uematsu M; Imataka G; Tanaka M; Okanishi T; Kubota T; Sudo A; Tohyama J; Tsuji M; Ohmori I; Naiki M; Hiraiwa-Sofue A; Sato H; Saitoh S; Shimizu T
    Epilepsia; 2012 Jan; 53(1):79-86. PubMed ID: 22092154
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations.
    Striano P; Mancardi MM; Biancheri R; Madia F; Gennaro E; Paravidino R; Beccaria F; Capovilla G; Dalla Bernardina B; Darra F; Elia M; Giordano L; Gobbi G; Granata T; Ragona F; Guerrini R; Marini C; Mei D; Longaretti F; Romeo A; Siri L; Specchio N; Vigevano F; Striano S; Tortora F; Rossi A; Minetti C; Dravet C; Gaggero R; Zara F
    Epilepsia; 2007 Jun; 48(6):1092-6. PubMed ID: 17381446
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Dravet syndrome with an exceptionally good seizure outcome in two adolescents.
    Kobayashi K; Ohmori I; Ouchida M; Ohtsuka Y
    Epileptic Disord; 2011 Sep; 13(3):340-4. PubMed ID: 21865128
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Dravet syndrome and SCN1A gene mutation related-epilepsies: cognitive impairment and its determinants.
    Guerrini R; Falchi M
    Dev Med Child Neurol; 2011 Apr; 53 Suppl 2():11-5. PubMed ID: 21504426
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Does a SCN1A gene mutation confer earlier age of onset of febrile seizures in GEFS+?
    Sijben AE; Sithinamsuwan P; Radhakrishnan A; Badawy RA; Dibbens L; Mazarib A; Lev D; Lerman-Sagie T; Straussberg R; Berkovic SF; Scheffer IE
    Epilepsia; 2009 Apr; 50(4):953-6. PubMed ID: 19292758
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cognitive development in children with Dravet syndrome.
    Ragona F
    Epilepsia; 2011 Apr; 52 Suppl 2():39-43. PubMed ID: 21463278
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Dravet syndrome (severe myoclonic epilepsy in infancy): a retrospective study of 16 patients.
    Korff C; Laux L; Kelley K; Goldstein J; Koh S; Nordli D
    J Child Neurol; 2007 Feb; 22(2):185-94. PubMed ID: 17621480
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Retrospective multiinstitutional study of the prevalence of early death in Dravet syndrome.
    Sakauchi M; Oguni H; Kato I; Osawa M; Hirose S; Kaneko S; Takahashi Y; Takayama R; Fujiwara T
    Epilepsia; 2011 Jun; 52(6):1144-9. PubMed ID: 21480880
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.