SUMMARYStem cell therapies are envisioned for severe neurologic disorders and intractable epilepsy. Methods to maintain and derive neural cells from embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) are providing insights into human nervous system development from stem cells and the future of stem cell therapy for epilepsy. For an expanded treatment of this topic A decade ago, the notion of regenerating severed arms or legs or restoring vision fell into the realm of biblical study or science fiction. However, advances in stem cell technology are encouraging the idea that some regeneration of the central nervous system (CNS) is attainable. Embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) show tremendous promise for repairing the damaged brain in epilepsy (Carpentino et al., 2008;Maisano et al., 2009).Stem cells are self-renewing and retain the potential to generate the three major CNS cell types-neurons, astrocytes, and oligodendrocytes. The brain's endogenous stem cells show limited capacity to replace injured or defective cell types. For intractable forms of epilepsy, stem cell-based therapies offer a novel approach for seizure suppression. Survival and integration of transplants of fetal c-aminobutyric acid (GABA)ergic progenitors or ESC-derived GABAergic progenitors in the developing brain of mouse models of epilepsy have provided evidence for the therapeutic potential of stem cell grafts for controlling intractable seizures .Many of the transcription factor codes that specify different cell types are known. This information is aiding efforts to direct stem cells toward specific lineages. Three main approaches have been developed for propagation: embryoid bodies, monolayer cultures, and neurosphere cultures. A challenge is obtaining neural stem cells with-defined regional identities that can be patterned into specific CNS lineages. Already it is possible to generate dopaminergic, motor, and GABAergic neurons from human ESCs. These cells can form neural rosettes that resemble the developing neural plate, and this stage shows greatest potential for neural patterning. Bacterial artificial chromosome (BAC) transgenesis is another novel tool that helps define and isolate specific neural and glial lineages (Maroof et al., 2010).Before clinical applications are realized, ''clinicalgrade'' human embryonic stem cells must be produced in xeno-free conditions and tumor formation must be reduced. Further roadblocks include achieving long-term survival of transplants and circumventing graft rejection. iPSCs remove immunological barriers to stem cell therapy, since iPSCs can be generated from a patient's own skin.