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 *

141 related articles for article (PubMed ID: 21488261)

  • 1. Novel human pathological mutations. Gene symbol: SCN1A. Disease: generalized epilepsy with febrile seizures plus.
    Chou IC; Lin WD; Tsai FJ
    Hum Genet; 2010 Apr; 127(4):484-5. PubMed ID: 21488261
    [No Abstract]   [Full Text] [Related]  

  • 2. Novel human pathological mutations. Gene symbol: SCN1A. Disease: generalized epilepsy with febrile seizures plus.
    Lin WD; Chou IC; Tsai FJ
    Hum Genet; 2010 Apr; 127(4):478. PubMed ID: 21488289
    [No Abstract]   [Full Text] [Related]  

  • 3. Novel human pathological mutations. Gene symbol: SCN1A. Disease: generalized epilepsy with febrile seizures plus.
    Chou IC; Lin WD; Tsai FJ
    Hum Genet; 2010 Apr; 127(4):481. PubMed ID: 21488303
    [No Abstract]   [Full Text] [Related]  

  • 4. Novel human pathological mutations. Gene symbol: SCN1A. Disease: generalized epilepsy with febrile seizures plus.
    Lin WD; Chou IC; Tsai FJ
    Hum Genet; 2010 Apr; 127(4):482. PubMed ID: 21488258
    [No Abstract]   [Full Text] [Related]  

  • 5. Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus.
    Annesi G; Gambardella A; Carrideo S; Incorpora G; Labate A; Pasqua AA; Civitelli D; Polizzi A; Annesi F; Spadafora P; Tarantino P; CirĂ² Candiano IC; Romeo N; De Marco EV; Ventura P; LePiane E; Zappia M; Aguglia U; Pavone L; Quattrone A
    Epilepsia; 2003 Sep; 44(9):1257-8. PubMed ID: 12919402
    [No Abstract]   [Full Text] [Related]  

  • 6. Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures.
    Fujiwara T; Sugawara T; Mazaki-Miyazaki E; Takahashi Y; Fukushima K; Watanabe M; Hara K; Morikawa T; Yagi K; Yamakawa K; Inoue Y
    Brain; 2003 Mar; 126(Pt 3):531-46. PubMed ID: 12566275
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus.
    Hawkins NA; Martin MS; Frankel WN; Kearney JA; Escayg A
    Neurobiol Dis; 2011 Mar; 41(3):655-60. PubMed ID: 21156207
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1A.
    Ito M; Nagafuji H; Okazawa H; Yamakawa K; Sugawara T; Mazaki-Miyazaki E; Hirose S; Fukuma G; Mitsudome A; Wada K; Kaneko S
    Epilepsy Res; 2002 Jan; 48(1-2):15-23. PubMed ID: 11823106
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Gene symbol: SCN1A. Disease: Generalized epilepsy with febrile seizures plus.
    Sun H; Zhang Y; Liang J; Liu X; Ma X; Wu H; Xu K; Qin J; Qi Y; Wu X
    Hum Genet; 2008 Oct; 124(3):298. PubMed ID: 18846618
    [No Abstract]   [Full Text] [Related]  

  • 10. SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus.
    Sun H; Zhang Y; Liang J; Liu X; Ma X; Wu H; Xu K; Qin J; Qi Y; Wu X
    J Hum Genet; 2008; 53(8):769-774. PubMed ID: 18566737
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Nav1.1 mutations cause febrile seizures associated with afebrile partial seizures.
    Sugawara T; Mazaki-Miyazaki E; Ito M; Nagafuji H; Fukuma G; Mitsudome A; Wada K; Kaneko S; Hirose S; Yamakawa K
    Neurology; 2001 Aug; 57(4):703-5. PubMed ID: 11524484
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Effect of localization of missense mutations in SCN1A on epilepsy phenotype severity.
    Kanai K; Hirose S; Oguni H; Fukuma G; Shirasaka Y; Miyajima T; Wada K; Iwasa H; Yasumoto S; Matsuo M; Ito M; Mitsudome A; Kaneko S
    Neurology; 2004 Jul; 63(2):329-34. PubMed ID: 15277629
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel inherited mutation in the voltage sensor region of SCN1A is associated with Panayiotopoulos syndrome in siblings and generalized epilepsy with febrile seizures plus.
    Livingston JH; Cross JH; Mclellan A; Birch R; Zuberi SM
    J Child Neurol; 2009 Apr; 24(4):503-8. PubMed ID: 19339291
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A family of generalized epilepsy with febrile seizures plus type 2-a new missense mutation of SCN1A found in the pedigree of several patients with complex febrile seizures.
    Nagao Y; Mazaki-Miyazaki E; Okamura N; Takagi M; Igarashi T; Yamakawa K
    Epilepsy Res; 2005 Feb; 63(2-3):151-6. PubMed ID: 15715999
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel de novo mutation of a conserved SCN1A amino-acid residue (R1596).
    Dlugos DJ; Ferraro TN; Buono RJ
    Pediatr Neurol; 2007 Oct; 37(4):303-5. PubMed ID: 17903680
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations.
    Bonanni P; Malcarne M; Moro F; Veggiotti P; Buti D; Ferrari AR; Parrini E; Mei D; Volzone A; Zara F; Heron SE; Bordo L; Marini C; Guerrini R
    Epilepsia; 2004 Feb; 45(2):149-58. PubMed ID: 14738422
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A missense mutation of the gene encoding voltage-dependent sodium channel (Nav1.1) confers susceptibility to febrile seizures in rats.
    Mashimo T; Ohmori I; Ouchida M; Ohno Y; Tsurumi T; Miki T; Wakamori M; Ishihara S; Yoshida T; Takizawa A; Kato M; Hirabayashi M; Sasa M; Mori Y; Serikawa T
    J Neurosci; 2010 Apr; 30(16):5744-53. PubMed ID: 20410126
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel SCN1A missense mutation causes generalized epilepsy with febrile seizures plus in a Chinese family.
    Cui X; Zeng F; Liu Y; Zhang J; Archacki S; Zhan T; Du R; Tang Z; Liu J; Wang QK; Liu M
    Neurosci Lett; 2011 Sep; 503(1):27-30. PubMed ID: 21843600
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms.
    Wallace RH; Hodgson BL; Grinton BE; Gardiner RM; Robinson R; Rodriguez-Casero V; Sadleir L; Morgan J; Harkin LA; Dibbens LM; Yamamoto T; Andermann E; Mulley JC; Berkovic SF; Scheffer IE
    Neurology; 2003 Sep; 61(6):765-9. PubMed ID: 14504318
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Progress in molecular genetics of generalized epilepsy with febrile seizures plus].
    Sun HH; Zhang YH
    Beijing Da Xue Xue Bao Yi Xue Ban; 2008 Apr; 40(2):229-33. PubMed ID: 18458705
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.