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 *

205 related articles for article (PubMed ID: 32062735)

  • 41. Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.
    Marini C; Mei D; Temudo T; Ferrari AR; Buti D; Dravet C; Dias AI; Moreira A; Calado E; Seri S; Neville B; Narbona J; Reid E; Michelucci R; Sicca F; Cross HJ; Guerrini R
    Epilepsia; 2007 Sep; 48(9):1678-1685. PubMed ID: 17561957
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Mutation spectrum of the SCN1A gene in a Hungarian population with epilepsy.
    Till Á; Zima J; Fekete A; Bene J; Czakó M; Szabó A; Melegh B; Hadzsiev K
    Seizure; 2020 Jan; 74():8-13. PubMed ID: 31765958
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Autism in several members of a family with generalized epilepsy with febrile seizures plus.
    Dixon-Salazar TJ; Keeler LC; Trauner DA; Gleeson JG
    J Child Neurol; 2004 Aug; 19(8):597-603. PubMed ID: 15605469
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Epilepsy-associated dysfunction in the voltage-gated neuronal sodium channel SCN1A.
    Lossin C; Rhodes TH; Desai RR; Vanoye CG; Wang D; Carniciu S; Devinsky O; George AL
    J Neurosci; 2003 Dec; 23(36):11289-95. PubMed ID: 14672992
    [TBL] [Abstract][Full Text] [Related]  

  • 45. NaV1.1 channels and epilepsy.
    Catterall WA; Kalume F; Oakley JC
    J Physiol; 2010 Jun; 588(Pt 11):1849-59. PubMed ID: 20194124
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Novel mutations in SCN9A occurring with fever-associated seizures or epilepsy.
    Ding J; Zhang JW; Guo YX; Zhang YX; Chen ZH; Zhai QX
    Seizure; 2019 Oct; 71():214-218. PubMed ID: 31394368
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. [Analysis of three Chinese pedigrees affected with Genetic epilepsy with febrile seizures plus due to variants of SCN1A gene].
    Yang Z; Wang Y; Chen G; Song L; Ma Y; Zhang W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Mar; 41(3):284-288. PubMed ID: 38448015
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A novel inherited SCN1A mutation associated with different neuropsychological phenotypes: is there a common core deficit?
    Passamonti C; Petrelli C; Mei D; Foschi N; Guerrini R; Provinciali L; Zamponi N
    Epilepsy Behav; 2015 Feb; 43():89-92. PubMed ID: 25569746
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Whole exome sequencing identifies a novel SCN1A mutation in genetic (idiopathic) generalized epilepsy and juvenile myoclonic epilepsy subtypes.
    Chan CK; Low JS; Lim KS; Low SK; Tan CT; Ng CC
    Neurol Sci; 2020 Mar; 41(3):591-598. PubMed ID: 31720899
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Sodium channel SCN1A and epilepsy: mutations and mechanisms.
    Escayg A; Goldin AL
    Epilepsia; 2010 Sep; 51(9):1650-8. PubMed ID: 20831750
    [TBL] [Abstract][Full Text] [Related]  

  • 52. SCN1A clinical spectrum includes the self-limited focal epilepsies of childhood.
    Kivity S; Oliver KL; Afawi Z; Damiano JA; Arsov T; Bahlo M; Berkovic SF
    Epilepsy Res; 2017 Mar; 131():9-14. PubMed ID: 28192756
    [TBL] [Abstract][Full Text] [Related]  

  • 53.
    Cornejo-Sanchez DM; Acharya A; Bharadwaj T; Marin-Gomez L; Pereira-Gomez P; Nouel-Saied LM; University Of Washington Center For Mendelian Genomics ; Nickerson DA; Bamshad MJ; Mefford HC; Schrauwen I; Carrizosa-Moog J; Cornejo-Ochoa W; Pineda-Trujillo N; Leal SM
    Genes (Basel); 2022 Apr; 13(5):. PubMed ID: 35627139
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Missense mutations in sodium channel SCN1A and SCN2A predispose children to encephalopathy with severe febrile seizures.
    Saitoh M; Ishii A; Ihara Y; Hoshino A; Terashima H; Kubota M; Kikuchi K; Yamanaka G; Amemiya K; Hirose S; Mizuguchi M
    Epilepsy Res; 2015 Nov; 117():1-6. PubMed ID: 26311622
    [TBL] [Abstract][Full Text] [Related]  

  • 55. A BAC transgenic mouse model reveals neuron subtype-specific effects of a Generalized Epilepsy with Febrile Seizures Plus (GEFS+) mutation.
    Tang B; Dutt K; Papale L; Rusconi R; Shankar A; Hunter J; Tufik S; Yu FH; Catterall WA; Mantegazza M; Goldin AL; Escayg A
    Neurobiol Dis; 2009 Jul; 35(1):91-102. PubMed ID: 19409490
    [TBL] [Abstract][Full Text] [Related]  

  • 56. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A knock-in model of human epilepsy in Drosophila reveals a novel cellular mechanism associated with heat-induced seizure.
    Sun L; Gilligan J; Staber C; Schutte RJ; Nguyen V; O'Dowd DK; Reenan R
    J Neurosci; 2012 Oct; 32(41):14145-55. PubMed ID: 23055484
    [TBL] [Abstract][Full Text] [Related]  

  • 58. From focal epilepsy to Dravet syndrome--Heterogeneity of the phenotype due to SCN1A mutations of the p.Arg1596 amino acid residue in the Nav1.1 subunit.
    Hoffman-Zacharska D; Szczepanik E; Terczynska I; Goszczanska-Ciuchta A; Zalewska-Miszkurka Z; Tataj R; Bal J
    Neurol Neurochir Pol; 2015; 49(4):258-66. PubMed ID: 26188943
    [TBL] [Abstract][Full Text] [Related]  

  • 59. SCN9A Epileptic Encephalopathy Mutations Display a Gain-of-function Phenotype and Distinct Sensitivity to Oxcarbazepine.
    Zhang S; Zhang Z; Shen Y; Zhu Y; Du K; Guo J; Ji Y; Tao J
    Neurosci Bull; 2020 Jan; 36(1):11-24. PubMed ID: 31372899
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A novel locus for generalized epilepsy with febrile seizures plus in French families.
    Baulac S; Gourfinkel-An I; Couarch P; Depienne C; Kaminska A; Dulac O; Baulac M; LeGuern E; Nabbout R
    Arch Neurol; 2008 Jul; 65(7):943-51. PubMed ID: 18625863
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.