Astrocytes are key homeostatic regulators in the central nervous system and play important
roles in physiology. After brain damage caused by eg, status epilepticus, traumatic brain …

Circadian rhythm disturbances are a common symptom among individuals with mood
disorders. The suprachiasmatic nucleus (SCN), in the ventral part of the anterior …

Alternating hemiplegia of childhood (AHC) is a rare, severe neurodevelopmental syndrome
characterized by recurrent hemiplegic episodes and distinct neurological manifestations …

Extracellular α‐synuclein (α‐syn) assemblies can be up‐taken by neurons; however, their
interaction with the plasma membrane and proteins has not been studied specifically. Here …

Cardiorespiratory collapse after a seizure is the leading cause of sudden unexpected death
in epilepsy (SUDEP) in young persons, but why only certain individuals are at risk is …

Na+/K+ pump or sodium-and potassium-activated adenosine 5'-triphosphatase (Na+, K+-
ATPase), its enzymatic version, is a crucial protein responsible for the electrochemical …

Genetic research has shown that mutations that modify the protein-coding sequence of
ATP1A3, the gene encoding the α 3 subunit of Na+/K+-ATPase, cause both rapid-onset …

Although dystonias are a common group of movement disorders, the mechanisms by which
brain dysfunction results in dystonia are not understood. Rapid-onset Dystonia …

Familial hemiplegic migraine type 2 (FHM2) is an autosomal dominant form of migraine with
aura that is caused by mutations of the α2-subunit of the Na, K-ATPase, an isoform almost …

Epilepsy is a common neurological disorder affecting approximately 1% of the population.
Mutations in voltage‐gated sodium channels are responsible for several monogenic …