276 related articles for article (PubMed ID: 28505490)
1. Heat induced temperature dysregulation and seizures in Dravet Syndrome/GEFS+ Gabrg2
Warner TA; Liu Z; Macdonald RL; Kang JQ
Epilepsy Res; 2017 Aug; 134():1-8. PubMed ID: 28505490
[TBL] [Abstract][Full Text] [Related]
2. Overexpressing wild-type γ2 subunits rescued the seizure phenotype in Gabrg2
Huang X; Zhou C; Tian M; Kang JQ; Shen W; Verdier K; Pimenta A; MacDonald RL
Epilepsia; 2017 Aug; 58(8):1451-1461. PubMed ID: 28586508
[TBL] [Abstract][Full Text] [Related]
3. Altered GABAA receptor expression in brainstem nuclei and SUDEP in Gabrg2(+/Q390X) mice associated with epileptic encephalopathy.
Xia G; P Pourali S; Warner TA; Zhang CQ; L Macdonald R; Kang JQ
Epilepsy Res; 2016 Jul; 123():50-4. PubMed ID: 27131289
[TBL] [Abstract][Full Text] [Related]
4. 4-Phenylbutyrate promoted wild-type γ-aminobutyric acid type A receptor trafficking, reduced endoplasmic reticulum stress, and mitigated seizures in Gabrg2
Shen W; Flamm C; Delahanty AJ; Casteel E; Biven M; DeLeeuw MB; Poliquin S; Nwosu G; Randhave K; Kang JQ
Epilepsia; 2024 Jan; 65(1):204-217. PubMed ID: 37746768
[TBL] [Abstract][Full Text] [Related]
5. The therapeutic effect of stiripentol in Gabrg2
Warner TA; Smith NK; Kang JQ
Epilepsy Res; 2019 Aug; 154():8-12. PubMed ID: 31022638
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Phenotype and SCN1A gene mutation screening in 39 families with generalized epilepsy with febrile seizures plus].
Xu XJ; Zhang YH; Sun HH; Liu XY; Wu HS; Wu XR
Zhonghua Er Ke Za Zhi; 2012 Aug; 50(8):580-6. PubMed ID: 23158734
[TBL] [Abstract][Full Text] [Related]
8. Fine Mapping of a Dravet Syndrome Modifier Locus on Mouse Chromosome 5 and Candidate Gene Analysis by RNA-Seq.
Hawkins NA; Zachwieja NJ; Miller AR; Anderson LL; Kearney JA
PLoS Genet; 2016 Oct; 12(10):e1006398. PubMed ID: 27768696
[TBL] [Abstract][Full Text] [Related]
9. Synergistic GABA-enhancing therapy against seizures in a mouse model of Dravet syndrome.
Oakley JC; Cho AR; Cheah CS; Scheuer T; Catterall WA
J Pharmacol Exp Ther; 2013 May; 345(2):215-24. PubMed ID: 23424217
[TBL] [Abstract][Full Text] [Related]
10. Modulating Endoplasmic Reticulum Chaperones and Mutant Protein Degradation in GABRG2(Q390X) Associated with Genetic Epilepsy with Febrile Seizures Plus and Dravet Syndrome.
Poliquin S; Nwosu G; Randhave K; Shen W; Flamm C; Kang JQ
Int J Mol Sci; 2024 Apr; 25(9):. PubMed ID: 38731820
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Cacna1g is a genetic modifier of epilepsy in a mouse model of Dravet syndrome.
Calhoun JD; Hawkins NA; Zachwieja NJ; Kearney JA
Epilepsia; 2017 Aug; 58(8):e111-e115. PubMed ID: 28556246
[TBL] [Abstract][Full Text] [Related]
13. Myoclonic Absence Seizures in Dravet Syndrome.
Myers KA; Scheffer IE
Pediatr Neurol; 2017 May; 70():67-69. PubMed ID: 28233668
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. GABRG2 Deletion Linked to Genetic Epilepsy with Febrile Seizures Plus Affects the Expression of GABA
Li X; Guo S; Liu K; Zhang C; Chang H; Yang W; Rong S; Hu Q; Cui J; Wang F; Sun T
Neuroscience; 2020 Jul; 438():116-136. PubMed ID: 32418750
[TBL] [Abstract][Full Text] [Related]
16. Sleep slow-wave oscillations trigger seizures in a genetic epilepsy model of Dravet syndrome.
Catron MA; Howe RK; Besing GK; St John EK; Potesta CV; Gallagher MJ; Macdonald RL; Zhou C
Brain Commun; 2023; 5(1):fcac332. PubMed ID: 36632186
[TBL] [Abstract][Full Text] [Related]
17. Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome.
Rubinstein M; Westenbroek RE; Yu FH; Jones CJ; Scheuer T; Catterall WA
Neurobiol Dis; 2015 Jan; 73():106-17. PubMed ID: 25281316
[TBL] [Abstract][Full Text] [Related]
18. Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant Dravet Syndrome model during development.
Tsai MS; Lee ML; Chang CY; Fan HH; Yu IS; Chen YT; You JY; Chen CY; Chang FC; Hsiao JH; Khorkova O; Liou HH; Yanagawa Y; Lee LJ; Lin SW
Neurobiol Dis; 2015 May; 77():35-48. PubMed ID: 25725421
[TBL] [Abstract][Full Text] [Related]
19. Donepezil increases resistance to induced seizures in a mouse model of Dravet syndrome.
Wong JC; Thelin JT; Escayg A
Ann Clin Transl Neurol; 2019 Aug; 6(8):1566-1571. PubMed ID: 31402621
[TBL] [Abstract][Full Text] [Related]
20. Dravet syndrome as part of the clinical and genetic spectrum of sodium channel epilepsies and encephalopathies.
Mei D; Cetica V; Marini C; Guerrini R
Epilepsia; 2019 Dec; 60 Suppl 3():S2-S7. PubMed ID: 31904125
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
