Detalhe da pesquisa
1.
Analysis of low-level somatic mosaicism reveals stage and tissue-specific mutational features in human development.
PLoS Genet;
18(9): e1010404, 2022 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36121845
2.
A machine learning-based quantitative model (LogBB_Pred) to predict the blood-brain barrier permeability (logBB value) of drug compounds.
Bioinformatics;
39(10)2023 10 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37713469
3.
Common genes and recurrent causative variants in 957 Asian patients with pediatric epilepsy.
Epilepsia;
65(3): 766-778, 2024 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38073125
4.
Genotypes and phenotypes of DNM1 encephalopathy.
J Med Genet;
60(11): 1076-1083, 2023 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37248033
5.
Eif2b3 mutants recapitulate phenotypes of vanishing white matter disease and validate novel disease alleles in zebrafish.
Hum Mol Genet;
30(5): 331-342, 2021 04 27.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33517449
6.
A decrease in the incidence of encephalitis in South Korea during the COVID-19 pandemic: A nationwide study between 2010 and 2021.
J Med Virol;
95(2): e28490, 2023 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36630084
7.
Disparate treatment outcomes according to presence of pathogenic mutations in West syndrome.
Epilepsia;
62(7): 1656-1664, 2021 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34008866
8.
The feasibility of performing multiple burr hole surgery in pediatric moyamoya patients as a response to failed mEDAS.
Childs Nerv Syst;
37(7): 2233-2238, 2021 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33755793
9.
Comparative Proteome Research in a Zebrafish Model for Vanishing White Matter Disease.
Int J Mol Sci;
22(5)2021 Mar 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33800130
10.
Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia.
Am J Hum Genet;
100(3): 454-472, 2017 Mar 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28215400
11.
Cannabidiol for Treating Lennox-Gastaut Syndrome and Dravet Syndrome in Korea.
J Korean Med Sci;
35(50): e427, 2020 Dec 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33372424
12.
Precise detection of low-level somatic mutation in resected epilepsy brain tissue.
Acta Neuropathol;
138(6): 901-912, 2019 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31377847
13.
Medication self-management and the quality of discharge education among parents of children with epilepsy.
Epilepsy Behav;
94: 14-19, 2019 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30884402
14.
Clobazam as an adjunctive treatment for infantile spasms.
Epilepsy Behav;
95: 161-165, 2019 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31059922
15.
Interregional metabolic connectivity of 2-deoxy-2[18 F]fluoro-D-glucose positron emission tomography in vagus nerve stimulation for pediatric patients with epilepsy: A retrospective cross-sectional study.
Epilepsia;
59(12): 2249-2259, 2018 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30370541
16.
Efficacy of the classic ketogenic and the modified Atkins diets in refractory childhood epilepsy.
Epilepsia;
57(1): 51-8, 2016 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26662710
17.
Changing name of epilepsy in Korea; cerebroelectric disorder (noi-jeon-jeung,ëì ì¦,): my epilepsy story.
Epilepsia;
55(3): 384-6, 2014 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24417228
18.
The impact of an exercise therapy on psychosocial health of children with benign epilepsy: a pilot study.
Epilepsy Behav;
37: 151-6, 2014 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25025685
19.
Epilepsy-related clinical factors and psychosocial functions in pediatric epilepsy.
Epilepsy Behav;
37: 43-8, 2014 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24972158
20.
Functional brain network analysis using electroencephalography in late-onset Lennox-Gastaut syndrome.
Epilepsy Res;
203: 107370, 2024 May 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38723341