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Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia.Audit of practice in sudden unexpected death in epilepsy (SUDEP) post mortems and neuropathological findings.When the face says it all: dysmorphology in identifying syndromic causes of epilepsy.Canine versus human epilepsy: are we up to date?Epilepsy diagnostic and treatment needs identified with a collaborative database involving tertiary centers in France.The "urban myth" of the association between neurological disorders and vaccinations.Overnight Video-Polysomnographic Studies in Children with Intractable Epileptic Encephalopathies
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Epilepsy: old syndromes, new genes.
@en
type
label
Epilepsy: old syndromes, new genes.
@en
prefLabel
Epilepsy: old syndromes, new genes.
@en
P2860
P1476
Epilepsy: old syndromes, new genes.
@en
P2093
Christian M Korff
P2860
P2888
P356
10.1007/S11910-014-0447-7
P577
2014-06-01T00:00:00Z
P5875
P6179
1052626775