Article info
PDFNeurological rarities
Brody disease: when myotonia is not myotonia
- Correspondence to Dr Luís Braz, Neurology Department, Centro Hospitalar Universitário de São João, Porto, Portugal; luispereirabraz{at}gmail.com
Citation
Brody disease: when myotonia is not myotonia
Publication history
- Received February 4, 2019
- Revised March 5, 2019
- Accepted March 12, 2019
- First published April 17, 2019.
Online issue publication
October 16, 2019
Article Versions
- Previous version (1 October 2019).
- 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
- Genetic neurological channelopathies: molecular genetics and clinical phenotypes
- Skeletal muscle channelopathies: a guide to diagnosis and management
- Muscle disease
- Muscle hypertrophy and pseudohypertrophy
- Focal and abnormally persistent paralysis associated with congenital paramyotonia
- Investigating the genetic susceptibility to exertional heat illness
- Diagnosis and new treatment in muscle channelopathies
- Redefining the clinical phenotypes of non-dystrophic myotonic syndromes
- Dominantly inherited proximal myotonic myopathy and leukoencephalopathy in a family with an incidental CLCN1 mutation
- Neurological channelopathies