about
Noninactivating voltage-gated sodium channels in severe myoclonic epilepsy of infancySingle-channel properties of human NaV1.1 and mechanism of channel dysfunction in SCN1A-associated epilepsyMolecular basis of an inherited epilepsyNav 1.4 slow-inactivation: is it a player in the warm-up phenomenon of myotonic disorders?Myotonia congenitaSCN8A encephalopathy: Research progress and prospectsNovel HCN2 mutation contributes to febrile seizures by shifting the channel's kinetics in a temperature-dependent mannerNeuroactive steroids for the treatment of status epilepticusAn algorithm for candidate sequencing in non-dystrophic skeletal muscle channelopathies.Altered fast and slow inactivation of the N440K Nav1.4 mutant in a periodic paralysis syndrome.Compromised function in the Na(v)1.2 Dravet syndrome mutation R1312T.Propofol hemisuccinate suppresses cortical spreading depression.Inhibition of astroglial Kir4.1 channels by selective serotonin reuptake inhibitors.Inhibition of astroglial inwardly rectifying Kir4.1 channels by a tricyclic antidepressant, nortriptyline.
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description
hulumtues
@sq
researcher
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wetenschapper
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հետազոտող
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name
Christoph Lossin
@ast
Christoph Lossin
@en
Christoph Lossin
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Christoph Lossin
@nl
Christoph Lossin
@sl
type
label
Christoph Lossin
@ast
Christoph Lossin
@en
Christoph Lossin
@es
Christoph Lossin
@nl
Christoph Lossin
@sl
prefLabel
Christoph Lossin
@ast
Christoph Lossin
@en
Christoph Lossin
@es
Christoph Lossin
@nl
Christoph Lossin
@sl
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P21
P31
P496
0000-0001-8101-2924