Lidocaine-dependent early infantile status epilepticus with highly suppressed EEG.
about
De novo mutations of voltage-gated sodium channel alphaII gene SCN2A in intractable epilepsiesGenetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.Truncation of the Shaker-like voltage-gated potassium channel, Kv1.1, causes megencephaly.Lidocaine treatment in pediatric convulsive status epilepticus
P2860
Lidocaine-dependent early infantile status epilepticus with highly suppressed EEG.
description
2002 nî lūn-bûn
@nan
2002 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2002年の論文
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2002年学术文章
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2002年学术文章
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2002年学术文章
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2002年学术文章
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2002年学术文章
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2002年學術文章
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name
Lidocaine-dependent early infantile status epilepticus with highly suppressed EEG.
@ast
Lidocaine-dependent early infantile status epilepticus with highly suppressed EEG.
@en
Lidocaine-dependent early infantile status epilepticus with highly suppressed EEG.
@nl
type
label
Lidocaine-dependent early infantile status epilepticus with highly suppressed EEG.
@ast
Lidocaine-dependent early infantile status epilepticus with highly suppressed EEG.
@en
Lidocaine-dependent early infantile status epilepticus with highly suppressed EEG.
@nl
prefLabel
Lidocaine-dependent early infantile status epilepticus with highly suppressed EEG.
@ast
Lidocaine-dependent early infantile status epilepticus with highly suppressed EEG.
@en
Lidocaine-dependent early infantile status epilepticus with highly suppressed EEG.
@nl
P2093
P2860
P1433
P1476
Lidocaine-dependent early infantile status epilepticus with highly suppressed EEG.
@en
P2093
Goro Takada
Masamichi Enoki
Tamami Yano
Yukio Sawaishi
P2860
P304
P356
10.1046/J.1528-1157.2002.25301.X
P577
2002-02-01T00:00:00Z