Molecular genetic decoding of malformations of cortical development
Jae-Seok LIM; Jeong-Ho LEE.
Journal of Genetic Medicine
; : 12-18, 2015.
Artículo en Inglés | WPRIM | ID: wpr-18091
Documentos relacionados
A developmental and genetic classification for malformations of cortical development: update 2012.
Focal cortical dysplasia: a practical guide for neurologists.
Technological and computational approaches to detect somatic mosaicism in epilepsy.
SLC35A2 somatic variants in drug resistant epilepsy: FCD and MOGHE.
The ILAE consensus classification of focal cortical dysplasia: An update proposed by an ad hoc task force of the ILAE diagnostic methods commission.
The clinico-pathological characterisation of focal cortical dysplasia type IIb genetically defined by MTOR mosaicism.
Junctional instability in neuroepithelium and network hyperexcitability in a focal cortical dysplasia human model.
Reorganization of Parvalbumin Immunopositive Perisomatic Innervation of Principal Cells in Focal Cortical Dysplasia Type IIB in Human Epileptic Patients.
Insight into developmental mechanisms of global and focal migration disorders of cortical development.
Focal cortical dysplasia pathology: diagnostic difficulty, classification, and utility for pathogenesis.