Infantile Epileptic Encephalopathies

Infantile Epileptic Encephalopathies

The phenotypic variability associated with sodium channel alpha 1 subunit gene SCN1A mutations was studied in 188 patients with various infantile epileptic encephalopathies referred to the Universities of Adelaide and Melbourne, Australia; and centres in Glasgow, UK; Wellington, New Zealand; Montrea...

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Bibliographic Details
Main Author: J Gordon Millichap
Format: Article
Language:English
Published: Pediatric Neurology Briefs Publishers 2007-04-01
Series:Pediatric Neurology Briefs
Subjects:
smei-borderland
myoclonic-astatic epilepsy
dravet syndrome
Online Access:https://www.pediatricneurologybriefs.com/articles/1035
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spelling doaj-61e7b2f0be2b4e259c99ce8718d2f4392020-11-25T02:40:12ZengPediatric Neurology Briefs PublishersPediatric Neurology Briefs1043-31552166-64822007-04-01214252610.15844/pedneurbriefs-21-4-11021Infantile Epileptic EncephalopathiesJ Gordon Millichap0Northwestern University Feinberg School of MedicineThe phenotypic variability associated with sodium channel alpha 1 subunit gene SCN1A mutations was studied in 188 patients with various infantile epileptic encephalopathies referred to the Universities of Adelaide and Melbourne, Australia; and centres in Glasgow, UK; Wellington, New Zealand; Montreal and Vancouver, Canada; Worcester, MD, USA, Israel, and Denmark.https://www.pediatricneurologybriefs.com/articles/1035smei-borderlandmyoclonic-astatic epilepsydravet syndrome
collection DOAJ
language English
format Article
sources DOAJ
author J Gordon Millichap
spellingShingle J Gordon Millichap
Infantile Epileptic Encephalopathies
Pediatric Neurology Briefs
smei-borderland
myoclonic-astatic epilepsy
dravet syndrome
author_facet J Gordon Millichap
author_sort J Gordon Millichap
title Infantile Epileptic Encephalopathies
title_short Infantile Epileptic Encephalopathies
title_full Infantile Epileptic Encephalopathies
title_fullStr Infantile Epileptic Encephalopathies
title_full_unstemmed Infantile Epileptic Encephalopathies
title_sort infantile epileptic encephalopathies
publisher Pediatric Neurology Briefs Publishers
series Pediatric Neurology Briefs
issn 1043-3155
2166-6482
publishDate 2007-04-01
description The phenotypic variability associated with sodium channel alpha 1 subunit gene SCN1A mutations was studied in 188 patients with various infantile epileptic encephalopathies referred to the Universities of Adelaide and Melbourne, Australia; and centres in Glasgow, UK; Wellington, New Zealand; Montreal and Vancouver, Canada; Worcester, MD, USA, Israel, and Denmark.
topic smei-borderland
myoclonic-astatic epilepsy
dravet syndrome
url https://www.pediatricneurologybriefs.com/articles/1035
work_keys_str_mv AT jgordonmillichap infantileepilepticencephalopathies
_version_ 1724782392876466176

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