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Cortical-area specific block of genetically determined absence seizures by et...
Absence epilepsy is characterised by a paroxysmal loss of consciousness, of abrupt onset and termination, and is associated with a bilateral synchronous spike and wave... -
A TASK3 channel (KCNK9) mutation in a genetic model of absence epilepsy.
Childhood absence epilepsy is an idiopathic, generalized, nonconvulsive epilepsy with a multifactorial genetic etiology. The KCNK9 gene coding for the TASK3 (Twik-like... -
Targeting thalamic nuclei is not sufficient for the full anti-absence action ...
Absence epilepsy is characterised by recurrent periods of physical and mental inactivity coupled to bilateral, synchronous spike and wave discharges (SWDs) on the... -
New analysis workflow for MALDI imaging mass spectrometry: application to the...
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