Mapping epileptic activity: sources or networks for the clinicians?
Epileptic seizures of focal origin are classically considered to arise from a focal
epileptogenic zone and then spread to other brain regions. This is a key concept for …
epileptogenic zone and then spread to other brain regions. This is a key concept for …
Electrical stimulation of the piriform cortex for the treatment of epilepsy: A review of the supporting evidence
In this review, we consider how the piriform cortex is engaged in both focal and generalized
epilepsy networks and postulate the various neural pathways that can be effectively …
epilepsy networks and postulate the various neural pathways that can be effectively …
15q13. 3 homozygous knockout mouse model display epilepsy-, autism-and schizophrenia-related phenotypes
A Forsingdal, K Fejgin, V Nielsen, T Werge… - Translational …, 2016 - nature.com
Abstract The 15q13. 3 microdeletion syndrome is caused by a 1.5-MB hemizygous
microdeletion located on 15q13. 3 affecting seven genes: FAN1; MTMR10; TRPM1; miR …
microdeletion located on 15q13. 3 affecting seven genes: FAN1; MTMR10; TRPM1; miR …
Optogenetic activation of the reticular nucleus of the thalamus attenuates limbic seizures via inhibition of the midline thalamus
E Wicker, PA Forcelli - Epilepsia, 2021 - Wiley Online Library
Objective The nucleus reticularis of the thalamus (nRT) is most studied in epilepsy for its role
in the genesis of absence seizures; much less is known regarding its role in other seizure …
in the genesis of absence seizures; much less is known regarding its role in other seizure …
Altered intrathalamic GABAA neurotransmission in a mouse model of a human genetic absence epilepsy syndrome
C Zhou, L Ding, ME Deel, EA Ferrick, RB Emeson… - Neurobiology of …, 2015 - Elsevier
We previously demonstrated that heterozygous deletion of Gabra1, the mouse homolog of
the human absence epilepsy gene that encodes the GABA A receptor (GABA AR) α1 …
the human absence epilepsy gene that encodes the GABA A receptor (GABA AR) α1 …
Cortical alterations in a model for absence epilepsy and febrile seizures: in vivo findings in mice carrying a human GABA (A) R gamma2 subunit mutation
Childhood absence epilepsy (CAE) is one of the most common forms of epilepsy among
children. The study of a large Australian family demonstrated that a point mutation in the …
children. The study of a large Australian family demonstrated that a point mutation in the …
Амигдала в системе регуляции репродуктивных функций организма при абсансной эпилепсии
ИИ Садртдинова, ЗР Хисматуллина - 2018 - elibrary.ru
В монографии изложены материалы по общей морфологии миндалевидного
комплекса и с помощью современного комплекса методов исследования дана оценка …
комплекса и с помощью современного комплекса методов исследования дана оценка …
T-Type Calcium Channels in Epilepsy
AS Sack, TP Snutch - Voltage-Gated Calcium Channels, 2022 - Springer
Epilepsy is a complex neurological disorder commonly thought to involve hyperexcitable
neurons that recruit neuronal populations within circuits to generate aberrant synchronous …
neurons that recruit neuronal populations within circuits to generate aberrant synchronous …
Cav3.2 T‐type calcium channel mutation influences kindling‐induced thalamic neuronal firing patterns in Genetic Absence Epilepsy Rats From Strasbourg
Objective Recent data indicate that amygdala kindling leads to significant changes in
interictal neuronal firing patterns of thalamic reticular nucleus (TRN) neurons by decreasing …
interictal neuronal firing patterns of thalamic reticular nucleus (TRN) neurons by decreasing …
Neuropeptide Y affects thalamic reticular nucleus neuronal firing and network synchronization associated with suppression of spike‐wave discharges
Summary Objectives Neuropeptide Y (NPY) potently suppresses spike‐wave discharges
(SWD s) in a genetic rat model of absence epilepsy (GAERS), but the underlying …
(SWD s) in a genetic rat model of absence epilepsy (GAERS), but the underlying …