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Journal Abstract Search

373 related items for PubMed ID: 30347190

  • 21. Mouse with Nav1.1 haploinsufficiency, a model for Dravet syndrome, exhibits lowered sociability and learning impairment.
    Ito S, Ogiwara I, Yamada K, Miyamoto H, Hensch TK, Osawa M, Yamakawa K.
    Neurobiol Dis; 2013 Jan; 49():29-40. PubMed ID: 22986304
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  • 25. Atypical myelinogenesis and reduced axon caliber in the Scn1a variant model of Dravet syndrome: An electron microscopy pilot study of the developing and mature mouse corpus callosum.
    Richards K, Jancovski N, Hanssen E, Connelly A, Petrou S.
    Brain Res; 2021 Jan 15; 1751():147157. PubMed ID: 33069731
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  • 27. Soticlestat, a novel cholesterol 24-hydroxylase inhibitor, reduces seizures and premature death in Dravet syndrome mice.
    Hawkins NA, Jurado M, Thaxton TT, Duarte SE, Barse L, Tatsukawa T, Yamakawa K, Nishi T, Kondo S, Miyamoto M, Abrahams BS, During MJ, Kearney JA.
    Epilepsia; 2021 Nov 15; 62(11):2845-2857. PubMed ID: 34510432
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  • 28. Life-span characterization of epilepsy and comorbidities in Dravet syndrome mice carrying a targeted deletion of exon 1 of the Scn1a gene.
    Gerbatin RR, Augusto J, Boutouil H, Reschke CR, Henshall DC.
    Exp Neurol; 2022 Aug 15; 354():114090. PubMed ID: 35487274
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  • 29. The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy.
    Martin MS, Tang B, Papale LA, Yu FH, Catterall WA, Escayg A.
    Hum Mol Genet; 2007 Dec 01; 16(23):2892-9. PubMed ID: 17881658
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  • 31. A high seizure burden increases several prostaglandin species in the hippocampus of a Scn1a+/- mouse model of Dravet syndrome.
    Zhou C, Satpute V, Yip KL, Anderson LL, Hawkins N, Kearney J, Arnold JC.
    Prostaglandins Other Lipid Mediat; 2024 Jun 01; 172():106836. PubMed ID: 38599513
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  • 32. 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 Jun 01; 49(4):258-66. PubMed ID: 26188943
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  • 36. A novel rat model of Dravet syndrome recapitulates clinical hallmarks.
    Li M, Yang L, Qian W, Ray S, Lu Z, Liu T, Zou YY, Naumann RK, Wang H.
    Neurobiol Dis; 2023 Aug 01; 184():106193. PubMed ID: 37295561
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  • 37. Clinical and molecular analysis of epilepsy-related genes in patients with Dravet syndrome.
    Jiang T, Shen Y, Chen H, Yuan Z, Mao S, Gao F.
    Medicine (Baltimore); 2018 Dec 01; 97(50):e13565. PubMed ID: 30558019
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  • 38. Genetics and clinical correlation of Dravet syndrome and its mimics - experience of a tertiary center in Taiwan.
    Liu YH, Cheng YT, Tsai MH, Chou IJ, Hung PC, Hsieh MY, Wang YS, Chen YJ, Kuo CY, Lin JJ, Wang HS, Lin KL.
    Pediatr Neonatol; 2021 Sep 01; 62(5):550-558. PubMed ID: 34226156
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  • 39. Antisense oligonucleotides increase Scn1a expression and reduce seizures and SUDEP incidence in a mouse model of Dravet syndrome.
    Han Z, Chen C, Christiansen A, Ji S, Lin Q, Anumonwo C, Liu C, Leiser SC, Meena, Aznarez I, Liau G, Isom LL.
    Sci Transl Med; 2020 Aug 26; 12(558):. PubMed ID: 32848094
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