Article info
A difficult case
Status epilepticus caused by an unusual encephalopathy
- Correspondence to Dr Michael Flower, University Hospital of Wales, Heath Park, Cardiff CF14 4XW, UK; michael.flower{at}cantab.net
Citation
Status epilepticus caused by an unusual encephalopathy
Publication history
- Accepted August 14, 2014
- First published September 10, 2014.
Online issue publication
April 14, 2016
Article Versions
- Previous version (14 April 2016).
- You are viewing the most recent version of this article.
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions
Other content recommended for you
- Late-onset mitochondrial encephalopathy with lactic acidosis and stroke-like episodes and the role of serial imaging
- Mitochondrial disease: mimics and chameleons
- Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) in the older adult
- Could it be mitochondrial? When and how to investigate
- Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies
- De novo mtDNA point mutations are common and have a low recurrence risk
- MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity
- Clinical mitochondrial genetics
- Preimplantation genetic diagnosis for mitochondrial DNA mutations: analysis of one blastomere suffices
- Diagnosis and therapy in neuromuscular disorders: diagnosis and new treatments in mitochondrial diseases