Article info
Neurological rarities
Relapsing necrotising encephalomyelopathy due to RANBP2 mutation
- Correspondence to Dr Erin Kelly, Neurology, Flinders Medical Centre, Adelaide, SA 5035, Australia; erin.kelly{at}sa.gov.au
Citation
Relapsing necrotising encephalomyelopathy due to RANBP2 mutation
Publication history
- Received August 6, 2018
- Revised November 30, 2018
- Accepted December 17, 2018
- First published February 22, 2019.
Online issue publication
June 23, 2020
Article Versions
- Previous version (23 June 2020).
- 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
© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.
Other content recommended for you
- Infectious encephalitis: mimics and chameleons
- Cortical abnormalities on MRI: what a neurologist should know
- Diagnostic value of cerebrospinal fluid analysis in a population of dogs with suspected idiopathic epilepsy
- A severe neurological complication of influenza in a previously well child
- Acute necrotising encephalopathy in a child with H1N1 influenza infection: a clinicoradiological diagnosis and follow-up
- Influenza A-associated acute necrotising encephalopathy in a 10-year-old child
- Acute disseminated encephalomyelitis: recognition in the hands of general paediatricians
- Rhomboencephalitis
- Adenovirus as a rare cause of acute necrotising encephalitis
- Mimics and chameleons in Guillain–Barré and Miller Fisher syndromes