Neonatal seizures and long QT Syndrome: A cardiocerebral channelopathy?-Reference-Cited by-同舟云学术

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Neonatal seizures and long QT Syndrome: A cardiocerebral channelopathy?

Published:2010-02 Issue:2 Volume:51 Page:293-296
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:

Author:

Heron Sarah E.,Hernandez Marta,Edwards Caitlin,Edkins Edward,Jansen Floor E.,Scheffer Ingrid E.,Berkovic Samuel F.,Mulley John C.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2009.02317.x/fullpdf

Reference12 articles.

1. New SCN5A mutation in a SUDEP victim with idiopathic epilepsy;Aurlien;Seizure,2009

2. Long QT Syndrome;Goldenberg;J Am Coll Cardiol,2008

3. Selective localization of cardiac SCN5A sodium channels in limbic regions of rat brain;Hartmann;Nat Neurosci,1999

4. Channelopathies in Idiopathic Epilepsy;Heron;Neurotherapeutics,2007

5. Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an SCN1A mutation;Hindocha;Epilepsia,2008

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1. Antiseizure medication and SUDEP – a need for unifying methodology in research;Frontiers in Neurology;2024-04-17

2. KCNH2 variants in a family with epilepsy and long QT syndrome: A case report and literature review;Epileptic Disorders;2023-06-04

3. Shades of a channelopathy—Hypoperfusion, excitability, or both: A case video;Epileptic Disorders;2023-05-24

4. SCN5A channelopathy: arrhythmia, cardiomyopathy, epilepsy and beyond;Philosophical Transactions of the Royal Society B: Biological Sciences;2023-05

5. Gene mutations in comorbidity of epilepsy and arrhythmia;Journal of Neurology;2022-11-14

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