Natálie Procházková

This study uses longitudinal imaging in a mouse model of FCD II to show lesion expansion, hypoactive dysmorphic neurons, and loss of pre-discharge neuronal recruitment over time.

The paper tracks how high-frequency oscillations evolve in a mouse model of focal cortical dysplasia type II, showing contralateral cortex recruitment into the epileptic network over time.

The paper tracks neuronal loss in an FCD mouse model and finds no reduction in seizures or neuron elimination with DQ treatment, suggesting strain-specific effects.

This study investigates seizure occurrence in FCD type II by analyzing lesion position and cytoarchitectural changes in a mouse model.