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Showing results 1 to 7 of 7

1
Brain Somatic Mutations in Epileptic Disorders

Koh, Hyun Yong; Lee, Jeong Ho, MOLECULES AND CELLS, v.41, no.10, pp.881 - 888, 2018-10

2
Deficiency of aminopeptidase P1 causes behavioral hyperactivity, cognitive deficits, and hippocampal neurodegeneration

Bae, Y. -S.; Yoon, S. H.; Han, J. Y.; Woo, J.; Cho, Y. S.; Kwon, S. -K.; Bae, Y. C.; et al, GENES BRAIN AND BEHAVIOR, v.17, no.2, pp.126 - 138, 2018-02

3
Efficacy of the Ketogenic Diet for Pediatric Epilepsy According to the Presence of Detectable Somatic mTOR Pathway Mutations in the Brain

Ko, Ara; Sim, Nam Suk; Choi, Han Som; Yang, Donghwa; Kim, Se Hee; Lee, Joon Soo; Kim, Dong Seok; et al, JOURNAL OF CLINICAL NEUROLOGY, v.18, no.1, pp.71 - 78, 2022-01

4
Role of the alpha 1G T-type calcium channel in spontaneous absence seizures in mutant mice

Song, Inseon; Kim, Daesoo; Choi, Soonwook; Sun, Minjeong; Kim, Yeongin; Shin, Hee-Sup, JOURNAL OF NEUROSCIENCE, v.24, no.22, pp.5249 - 5257, 2004-06

5
Slc6a20a Heterozygous and Homozygous Mutant Mice Display Differential Behavioral and Transcriptomic Changes

Kim, Junhyung; Roh, Junyeop Daniel; Kim, Seongbin; Kang, Hyojin; Bae, Mihyun; Kim, Eunjoon, FRONTIERS IN MOLECULAR NEUROSCIENCE, v.15, 2022-03

6
The ILAE consensus classification of focal cortical dysplasia: An update proposed by an ad hoc task force of the ILAE diagnostic methods commission

Najm, Imad; Lal, Dennis; Alonso Vanegas, Mario; Cendes, Fernando; Lopes-Cendes, Iscia; Palmini, Andre; Paglioli, Eliseu; et al, EPILEPSIA, v.63, no.8, pp.1899 - 1919, 2022-08

7
Toward a better definition of focal cortical dysplasia: An iterative histopathological and genetic agreement trial

Bluemcke, Ingmar; Coras, Roland; Busch, Robyn M.; Morita-Sherman, Marcia; Lal, Dennis; Prayson, Richard; Cendes, Fernando; et al, EPILEPSIA, v.62, no.6, pp.1416 - 1428, 2021-06

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