BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

180 related articles for article (PubMed ID: 21504428)

  • 1. Overall management of patients with Dravet syndrome.
    Ceulemans B
    Dev Med Child Neurol; 2011 Apr; 53 Suppl 2():19-23. PubMed ID: 21504428
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Coping with Dravet syndrome: parental experiences with a catastrophic epilepsy.
    Nolan KJ; Camfield CS; Camfield PR
    Dev Med Child Neurol; 2006 Sep; 48(9):761-5. PubMed ID: 16904024
    [TBL] [Abstract][Full Text] [Related]  

  • 3. "Severe myoclonic epilepsy in infancy". Relevance for the clinician of severe epilepsy starting in infancy.
    Ceulemans B; Cras P
    Acta Neurol Belg; 2004 Sep; 104(3):95-9. PubMed ID: 15508261
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Dravet syndrome and parent associations: the IDEA League experience with comorbid conditions, mortality, management, adaptation, and grief.
    Skluzacek JV; Watts KP; Parsy O; Wical B; Camfield P
    Epilepsia; 2011 Apr; 52 Suppl 2():95-101. PubMed ID: 21463290
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Severe myoclonic epilepsy in infancy (Dravet's syndrome). Its nosological characteristics and therapeutic aspects].
    Nieto Barrera M; Candau Fernandez Mensaque R; Nieto Jiménez M
    Rev Neurol; 2003 Jul 1-15; 37(1):64-8. PubMed ID: 12861512
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Developmental outcome in benign myoclonic epilepsy in infancy and reflex myoclonic epilepsy in infancy: a literature review and six new cases.
    Zuberi SM; O'Regan ME
    Epilepsy Res; 2006 Aug; 70 Suppl 1():S110-5. PubMed ID: 16904290
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dravet syndrome: the long-term outcome.
    Genton P; Velizarova R; Dravet C
    Epilepsia; 2011 Apr; 52 Suppl 2():44-9. PubMed ID: 21463279
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Helping families cope with the devastation of Dravet syndrome.
    Camfield P; Camfield C; Nolan K
    Eur J Paediatr Neurol; 2012 Sep; 16 Suppl 1():S9-12. PubMed ID: 22695036
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Coping with a child with Dravet syndrome: insights from families.
    Nolan K; Camfield CS; Camfield PR
    J Child Neurol; 2008 Jun; 23(6):690-4. PubMed ID: 18344453
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The core Dravet syndrome phenotype.
    Dravet C
    Epilepsia; 2011 Apr; 52 Suppl 2():3-9. PubMed ID: 21463272
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Helping Families Cope with the Severe Stress of Dravet Syndrome.
    Camfield P; Camfield C; Nolan K
    Can J Neurol Sci; 2016 Jun; 43 Suppl 3():S9-S12. PubMed ID: 27264140
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Addressing the needs of patients and their family: conclusion.
    Dravet C
    Eur J Paediatr Neurol; 2012 Sep; 16 Suppl 1():S18-20. PubMed ID: 22695037
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dravet syndrome history.
    Dravet C
    Dev Med Child Neurol; 2011 Apr; 53 Suppl 2():1-6. PubMed ID: 21504424
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. [Severe myoclonic epilepsy in infancy. Clinical and paraclinical aspects].
    Martínez-Bermejo A; López-Martín V; Arcas J; Tendero A; Roche Herrero MC; Merino M
    Rev Neurol; 2003 Jul 1-15; 37(1):55-9. PubMed ID: 12861510
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.