133 related articles for article (PubMed ID: 37984419)
1. Seizure Control Outcomes following Resection of Cortical Dysplasia in Patients with DEPDC5 Variants: A Systematic Review and Individual Patient Data Analysis.
McGinley C; Teti S; Hofmann K; Schreiber JM; Cohen NT; Gaillard WD; Oluigbo CO
Neuropediatrics; 2024 Feb; 55(1):1-8. PubMed ID: 37984419
[TBL] [Abstract][Full Text] [Related]
2. DEPDC5 plays a vital role in epilepsy: Genotypic and phenotypic features in cohort and literature.
Gu C; Wei X; Yan D; Cai Y; Li D; Shu J; Cai C
Epileptic Disord; 2024 Jun; 26(3):341-349. PubMed ID: 38752894
[TBL] [Abstract][Full Text] [Related]
3. Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia.
Weckhuysen S; Marsan E; Lambrecq V; Marchal C; Morin-Brureau M; An-Gourfinkel I; Baulac M; Fohlen M; Kallay Zetchi C; Seeck M; de la Grange P; Dermaut B; Meurs A; Thomas P; Chassoux F; Leguern E; Picard F; Baulac S
Epilepsia; 2016 Jun; 57(6):994-1003. PubMed ID: 27173016
[TBL] [Abstract][Full Text] [Related]
4. Epilepsy surgery outcomes in patients with GATOR1 gene complex variants: Report of new cases and review of literature.
Sahly AN; Whitney R; Costain G; Chau V; Otsubo H; Ochi A; Donner EJ; Cunningham J; Jones KC; Widjaja E; Ibrahim GM; Jain P
Seizure; 2023 Apr; 107():13-20. PubMed ID: 36931189
[TBL] [Abstract][Full Text] [Related]
5. DEPDC5 mutations in familial and sporadic focal epilepsy.
Tsai MH; Chan CK; Chang YC; Yu YT; Chuang ST; Fan WL; Li SC; Fu TY; Chang WN; Liou CW; Chuang YC; Ng CC; Hwang DY; Lim KS
Clin Genet; 2017 Oct; 92(4):397-404. PubMed ID: 28170089
[TBL] [Abstract][Full Text] [Related]
6. Long-term seizure outcome in 211 patients with focal cortical dysplasia.
Fauser S; Essang C; Altenmüller DM; Staack AM; Steinhoff BJ; Strobl K; Bast T; Schubert-Bast S; Stephani U; Wiegand G; Prinz M; Brandt A; Zentner J; Schulze-Bonhage A
Epilepsia; 2015 Jan; 56(1):66-76. PubMed ID: 25495786
[TBL] [Abstract][Full Text] [Related]
7. Familial focal epilepsy with focal cortical dysplasia due to DEPDC5 mutations.
Baulac S; Ishida S; Marsan E; Miquel C; Biraben A; Nguyen DK; Nordli D; Cossette P; Nguyen S; Lambrecq V; Vlaicu M; Daniau M; Bielle F; Andermann E; Andermann F; Leguern E; Chassoux F; Picard F
Ann Neurol; 2015 Apr; 77(4):675-83. PubMed ID: 25623524
[TBL] [Abstract][Full Text] [Related]
8. A mouse model of DEPDC5-related epilepsy: Neuronal loss of Depdc5 causes dysplastic and ectopic neurons, increased mTOR signaling, and seizure susceptibility.
Yuskaitis CJ; Jones BM; Wolfson RL; Super CE; Dhamne SC; Rotenberg A; Sabatini DM; Sahin M; Poduri A
Neurobiol Dis; 2018 Mar; 111():91-101. PubMed ID: 29274432
[TBL] [Abstract][Full Text] [Related]
9. Clinical and genetic features of GATOR1 complex-associated epilepsy.
Yin K; Lei X; Yan Z; Yang Y; Deng Q; Lu Q; Zhang X; Wang M; Liu Q
J Med Genet; 2023 Aug; 60(8):784-790. PubMed ID: 36604176
[TBL] [Abstract][Full Text] [Related]
10. DEPDC5-related epilepsy: A comprehensive review.
Samanta D
Epilepsy Behav; 2022 May; 130():108678. PubMed ID: 35429726
[TBL] [Abstract][Full Text] [Related]
11. Genetic testing in children enrolled in epilepsy surgery program. A real-life study.
Straka B; Splitkova B; Vlckova M; Tesner P; Rezacova H; Krskova L; Koblizek M; Kyncl M; Maulisova A; Bukacova K; Uhrova-Meszarosova A; Musilova A; Kudr M; Ebel M; Belohlavkova A; Jahodova A; Liby P; Tichy M; Jezdik P; Zamecnik J; Aronica E; Krsek P
Eur J Paediatr Neurol; 2023 Nov; 47():80-87. PubMed ID: 37812946
[TBL] [Abstract][Full Text] [Related]
12. Surgery for epilepsy.
West S; Nevitt SJ; Cotton J; Gandhi S; Weston J; Sudan A; Ramirez R; Newton R
Cochrane Database Syst Rev; 2019 Jun; 6(6):CD010541. PubMed ID: 31237346
[TBL] [Abstract][Full Text] [Related]
13. What is the impact of a novel DEPDC5 variant on an infant with focal epilepsy: a case report.
Gu C; Lu X; Ma J; Pu L; Zhi X; Shu J; Li D; Cai C
BMC Pediatr; 2022 Jul; 22(1):459. PubMed ID: 35907814
[TBL] [Abstract][Full Text] [Related]
14. Seizure features and outcomes in 50 children with GATOR1 variants: A retrospective study, more favorable for epilepsy surgery.
Wang H; Liu W; Zhang Y; Liu Q; Cai L; Jiang Y
Epilepsia Open; 2023 Sep; 8(3):969-979. PubMed ID: 37259768
[TBL] [Abstract][Full Text] [Related]
15. [Genotype and phenotype of children with DEPDC5 gene variants related epilepsy].
Liu WW; Yang Y; Niu XY; Cheng MM; Wang S; Wu Y; Yang ZX; Liu XY; Cai LX; Jiang YW; Zhang YH
Zhonghua Er Ke Za Zhi; 2021 Oct; 59(10):859-864. PubMed ID: 34587683
[No Abstract] [Full Text] [Related]
16. Second-hit mosaic mutation in mTORC1 repressor DEPDC5 causes focal cortical dysplasia-associated epilepsy.
Ribierre T; Deleuze C; Bacq A; Baldassari S; Marsan E; Chipaux M; Muraca G; Roussel D; Navarro V; Leguern E; Miles R; Baulac S
J Clin Invest; 2018 Jun; 128(6):2452-2458. PubMed ID: 29708508
[TBL] [Abstract][Full Text] [Related]
17. Everolimus precision therapy for the GATOR1-related epilepsies: A case series.
Moloney PB; Kearney H; Benson KA; Costello DJ; Cavalleri GL; Gorman KM; Lynch BJ; Delanty N
Eur J Neurol; 2023 Oct; 30(10):3341-3346. PubMed ID: 37422919
[TBL] [Abstract][Full Text] [Related]
18. Magnetoencephalogram-assisted diagnosis of familial focal epilepsy with variable foci in a Chinese family with a novel DEPDC5 mutation.
Li M; Huang Z; Zhang X; Duan Y; Jia Y; Ye J; Wang Y
Epileptic Disord; 2019 Jun; 21(3):289-294. PubMed ID: 31225799
[TBL] [Abstract][Full Text] [Related]
19. The clinical, imaging, pathological and genetic landscape of bottom-of-sulcus dysplasia.
Macdonald-Laurs E; Warren AEL; Francis P; Mandelstam SA; Lee WS; Coleman M; Stephenson SEM; Barton S; D'Arcy C; Lockhart PJ; Leventer RJ; Harvey AS
Brain; 2024 Apr; 147(4):1264-1277. PubMed ID: 37939785
[TBL] [Abstract][Full Text] [Related]
20. The landscape of epilepsy-related GATOR1 variants.
Baldassari S; Picard F; Verbeek NE; van Kempen M; Brilstra EH; Lesca G; Conti V; Guerrini R; Bisulli F; Licchetta L; Pippucci T; Tinuper P; Hirsch E; de Saint Martin A; Chelly J; Rudolf G; Chipaux M; Ferrand-Sorbets S; Dorfmüller G; Sisodiya S; Balestrini S; Schoeler N; Hernandez-Hernandez L; Krithika S; Oegema R; Hagebeuk E; Gunning B; Deckers C; Berghuis B; Wegner I; Niks E; Jansen FE; Braun K; de Jong D; Rubboli G; Talvik I; Sander V; Uldall P; Jacquemont ML; Nava C; Leguern E; Julia S; Gambardella A; d'Orsi G; Crichiutti G; Faivre L; Darmency V; Benova B; Krsek P; Biraben A; Lebre AS; Jennesson M; Sattar S; Marchal C; Nordli DR; Lindstrom K; Striano P; Lomax LB; Kiss C; Bartolomei F; Lepine AF; Schoonjans AS; Stouffs K; Jansen A; Panagiotakaki E; Ricard-Mousnier B; Thevenon J; de Bellescize J; Catenoix H; Dorn T; Zenker M; Müller-Schlüter K; Brandt C; Krey I; Polster T; Wolff M; Balci M; Rostasy K; Achaz G; Zacher P; Becher T; Cloppenborg T; Yuskaitis CJ; Weckhuysen S; Poduri A; Lemke JR; Møller RS; Baulac S
Genet Med; 2019 Feb; 21(2):398-408. PubMed ID: 30093711
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
