Detalhe da pesquisa
1.
Early Treatment with Vigabatrin Does Not Decrease Focal Seizures or Improve Cognition in Tuberous Sclerosis Complex: The PREVeNT Trial.
Ann Neurol
; 2023 Aug 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37638552
2.
Expanding eligibility for intracranial electroencephalography using Dexmedetomidine Hydrochloride in children with behavioral dyscontrol.
Epilepsy Behav
; 150: 109541, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38035536
3.
Somatic variants in diverse genes leads to a spectrum of focal cortical malformations.
Brain
; 145(8): 2704-2720, 2022 08 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-35441233
4.
Antiseizure medication use and medical resource utilization after resective epilepsy surgery in children in the United States: A contemporary nationwide cross-sectional cohort analysis.
Epilepsia
; 63(4): 824-835, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35213744
5.
Caregivers' impression of epilepsy surgery in patients with tuberous sclerosis complex.
Epilepsy Behav
; 111: 107331, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32759076
6.
Postoperative outcomes following pediatric intracranial electrode monitoring: A case for stereoelectroencephalography (SEEG).
Epilepsy Behav
; 104(Pt A): 106905, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32028127
7.
Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy.
Ann Neurol
; 83(6): 1133-1146, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29679388
8.
Response Letter to the Editor: "Expanding eligibility for intracranial electroencephalography using dexmedetomidine hydrochloride in children with behavioral dyscontrol".
Epilepsy Behav
; 153: 109657, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38368786
9.
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies.
Brain
; 140(9): 2337-2354, 2017 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29050392
10.
Delay in pediatric epilepsy surgery: A caregiver's perspective.
Epilepsy Behav
; 78: 175-178, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29126702
11.
Analyses of SLC13A5-epilepsy patients reveal perturbations of TCA cycle.
Mol Genet Metab
; 121(4): 314-319, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28673551
12.
Interictal network synchrony and local heterogeneity predict epilepsy surgery outcome among pediatric patients.
Epilepsia
; 58(3): 402-411, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28166392
13.
Mutations in the Na(+)/citrate cotransporter NaCT (SLC13A5) in pediatric patients with epilepsy and developmental delay.
Mol Med
; 222016 05 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-27261973
14.
A potential role for glia-derived extracellular matrix remodeling in postinjury epilepsy.
J Neurosci Res
; 94(9): 794-803, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27265805
15.
Plasma taurine levels are not affected by vigabatrin in pediatric patients.
Epilepsia
; 57(8): e168-72, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27344989
16.
Suppressing cAMP response element-binding protein transcription shortens the duration of status epilepticus and decreases the number of spontaneous seizures in the pilocarpine model of epilepsy.
Epilepsia
; 56(12): 1870-8, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26419901
17.
Perineuronal net degradation in epilepsy.
Epilepsia
; 56(7): 1124-33, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26032766
18.
Approach, complications, and outcomes for 37 consecutive pediatric patients undergoing laser ablation for medically refractory epilepsy at Stanford Children's Health.
J Neurosurg Pediatr
; 33(1): 1-11, 2024 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37922561
19.
MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways.
Neurogenetics
; 14(2): 99-111, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23389741
20.
Language Dysfunction in Pediatric Epilepsy.
J Pediatr
; 194: 13-21, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29241678