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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

486 related items for PubMed ID: 16359471

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?
    Scheffer IE, Zhang YH, Jansen FE, Dibbens L.
    Brain Dev; 2009 May; 31(5):394-400. PubMed ID: 19203856
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Sodium and potassium channel dysfunctions in rare and common idiopathic epilepsy syndromes.
    Hahn A, Neubauer BA.
    Brain Dev; 2009 Aug; 31(7):515-20. PubMed ID: 19464834
    [Abstract] [Full Text] [Related]

  • 7. Genes and mutations in idiopathic epilepsy.
    Steinlein OK.
    Am J Med Genet; 2001 Aug; 106(2):139-45. PubMed ID: 11579434
    [Abstract] [Full Text] [Related]

  • 8. Febrile seizures, genetic (generalized) epilepsy with febrile seizures plus, and Dravet's syndrome.
    Scanlon A, Cook SS.
    J Spec Pediatr Nurs; 2010 Apr; 15(2):154-9. PubMed ID: 20367785
    [Abstract] [Full Text] [Related]

  • 9. [Linkage location and mutation analysis of generalized epilepsy with febrile seizures plus].
    Lin H, Wang YP, Wang MY, Wu LW.
    Zhonghua Yi Xue Za Zhi; 2008 Dec 09; 88(45):3177-81. PubMed ID: 19171087
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Generalized epilepsy with febrile seizures plus (GEFS+) spectrum: clinical manifestations and SCN1A mutations in Indonesian patients.
    Herini ES, Gunadi, Harahap IS, Yusoff S, Morikawa S, Patria SY, Nishimura N, Sunartini, Sutaryo, Takada S, Matsuo M, Nishio H.
    Epilepsy Res; 2010 Jun 09; 90(1-2):132-9. PubMed ID: 20452746
    [Abstract] [Full Text] [Related]

  • 13. Generalized epilepsy with febrile seizures plus: novel SCN1A mutation.
    Dimova PS, Yordanova I, Bojinova V, Jordanova A, Kremenski I.
    Pediatr Neurol; 2010 Feb 09; 42(2):137-40. PubMed ID: 20117752
    [Abstract] [Full Text] [Related]

  • 14. Novel de novo splice-site mutation of SCN1A in a patient with partial epilepsy with febrile seizures plus.
    Kumakura A, Ito M, Hata D, Oh N, Kurahashi H, Wang JW, Hirose S.
    Brain Dev; 2009 Feb 09; 31(2):179-82. PubMed ID: 18632234
    [Abstract] [Full Text] [Related]

  • 15. Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance.
    Zara F, Specchio N, Striano P, Robbiano A, Gennaro E, Paravidino R, Vanni N, Beccaria F, Capovilla G, Bianchi A, Caffi L, Cardilli V, Darra F, Bernardina BD, Fusco L, Gaggero R, Giordano L, Guerrini R, Incorpora G, Mastrangelo M, Spaccini L, Laverda AM, Vecchi M, Vanadia F, Veggiotti P, Viri M, Occhi G, Budetta M, Taglialatela M, Coviello DA, Vigevano F, Minetti C.
    Epilepsia; 2013 Mar 09; 54(3):425-36. PubMed ID: 23360469
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. A case of extended spectrum GEFS+.
    Grant AC, Vazquez B.
    Epilepsia; 2005 Mar 09; 46 Suppl 10():39-40. PubMed ID: 16359470
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 25.