about
Electrogenic tuning of the axon initial segmentDuration of culture and sonic hedgehog signaling differentially specify PV versus SST cortical interneuron fates from embryonic stem cellsThe CD26-related dipeptidyl aminopeptidase-like protein DPPX is a critical component of neuronal A-type K+ channelsComplementary control of sensory adaptation by two types of cortical interneuronsRapid developmental maturation of neocortical FS cell intrinsic excitability.K+ channels at the axon initial segment dampen near-threshold excitability of neocortical fast-spiking GABAergic interneuronsRespiratory failure, cleft palate and epilepsy in the mouse model of human Xq22.1 deletion syndrome.Anti-N-methyl-D-aspartate receptor-mediated encephalitis in infants and toddlers: case report and review of the literature.Mechanisms of epileptogenesis: a convergence on neural circuit dysfunction.A patient with lissencephaly, developmental delay, and infantile spasms, due to de novo heterozygous mutation of KIF2A.Alexia due to ischemic stroke of the visual word form area.Prenatal diagnosis of hemimegalencephaly.Specific functions of synaptically localized potassium channels in synaptic transmission at the neocortical GABAergic fast-spiking cell synapse.Smaller anterior hippocampal formation volume in antipsychotic-naive patients with first-episode schizophrenia.Seizure and altered mental status in a 12-year-old child with Shigella sonnei gastroenteritis.Pontine tegmental cap dysplasia: neuropathological confirmation of a rare clinical/radiological syndrome.Reply to "Recurrent SCN3A p.Ile875Thr variant in patients with polymicrogyria"Mutations in SCN3A cause early infantile epileptic encephalopathyA Transient Developmental Window of Fast-Spiking Interneuron Dysfunction in a Mouse Model of Dravet Syndrome.Vasoactive intestinal peptide-expressing interneurons are impaired in a mouse model of Dravet syndromeSeizing the opportunity: stem cells take on epilepsyTargeted treatment of migrating partial seizures of infancy with quinidineConfirming an expanded spectrum of SCN2A mutations: a case seriesInterneuron Desynchronization Precedes Seizures in a Mouse Model of Dravet SyndromeSpectrum of KV 2.1 Dysfunction in KCNB1-Associated Neurodevelopmental DisordersMitochondrial deficits in human iPSC-derived neurons from patients with 22q11.2 deletion syndrome and schizophreniaA single-center SCN8A-related epilepsy cohort: clinical, genetic, and physiologic characterizationSCN3A-related neurodevelopmental disorder: A spectrum of epilepsy and brain malformation
P50
Q24634301-15207369-A7B2-42B9-A838-4B6A20AE8388Q27346704-8F858A62-F82C-44A5-8777-FF9B2FA147D6Q28568564-9FEC19DE-751F-4DB1-9F91-AD271A3B3817Q30398925-77643216-D2FD-4E15-BBC7-2BA83A52D84AQ30428037-1C7A4E1D-D14F-414E-AA1A-19394B2887B7Q30438904-93605867-745A-4A26-9772-212DF94C2D35Q30581149-60DD8235-58EB-463F-949C-393D8E637F7EQ30710506-05B18E76-9C95-4A74-AAE4-95564F002D76Q34339959-41578741-2318-4635-B6FF-6BEF11FAB13CQ37427210-74821E94-5B4A-43E1-9B33-DB51743687C0Q45846815-C5D41394-91CC-4592-A23D-ACD8A4587D5DQ46076772-7B4DB776-542F-489B-B425-32649BD61CBDQ46510763-3180E201-A297-4F68-B342-10DC5B6A1268Q48135249-EC1FE94A-6BDB-468F-8E24-F91A67232B59Q51816171-941A86E6-FAC9-4113-81C4-EF6B30A15523Q52150084-4B52AF81-FE29-406F-A475-32A9DD931E61Q56232632-3E356E6D-021E-471D-8BEE-3F3FCD80BF3DQ56232635-2BFB940F-13BE-48F0-A516-247490FA155EQ64967262-81F1C778-E4A9-43A0-A3F6-2417BA7DEC41Q83231448-9FC7EE5C-3BEF-46AD-9240-5B1A57226045Q86318992-A53B4EA6-A485-4BB1-A534-9F13D33AC465Q87416228-806E4C0B-B4EC-42DF-B816-32E985A03BE3Q87499910-EE7233F9-0301-436C-B0D3-043BEC85413DQ89899631-1ED8964F-80FF-4DED-A10F-9981F0B1FAE5Q90632366-FEA6D8FB-0E61-430F-911A-4838699AB8B8Q91329654-6436D561-8BDF-4F38-9CDB-E081F088A3FFQ92554643-E18FFAD4-9E81-491E-B200-3C6F3F23F512Q96219518-B24C19BC-5041-4B30-A5C3-2841C268EDF3
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Ethan M Goldberg
@ast
Ethan M Goldberg
@en
Ethan M Goldberg
@es
Ethan M Goldberg
@nl
Ethan M Goldberg
@sl
type
label
Ethan M Goldberg
@ast
Ethan M Goldberg
@en
Ethan M Goldberg
@es
Ethan M Goldberg
@nl
Ethan M Goldberg
@sl
prefLabel
Ethan M Goldberg
@ast
Ethan M Goldberg
@en
Ethan M Goldberg
@es
Ethan M Goldberg
@nl
Ethan M Goldberg
@sl
P106
P31
P496
0000-0002-7404-735X