Article info
PDFNeurological rarities
Remarkable motor recovery after riboflavin therapy in adult-onset Brown—Vialetto—Van Laere syndrome
- Correspondence to Dr James A Bashford, Maurice Wohl Clinical Neuroscience Institute, King's College London, Institute of Psychiatry, Psychology & Neuroscience, 5 Cutcombe Road, Camberwell, London SE5 9RX, UK; james.bashford{at}kcl.ac.uk
Citation
Remarkable motor recovery after riboflavin therapy in adult-onset Brown—Vialetto—Van Laere syndrome
Publication history
- Accepted September 12, 2016
- First published October 24, 2016.
Online issue publication
January 17, 2017
Article Versions
- Previous version (24 October 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://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Other content recommended for you
- Brown-Vialetto-Van Laere syndrome: a novel diagnosis to a common presentation
- Riboflavin transporter 3 involvement in infantile Brown-Vialetto-Van Laere disease: two novel mutations
- Brown-Vialetto-Van Laere syndrome: a 28-year follow-up
- Late-onset riboflavin transporter deficiency: a treatable mimic of various motor neuropathy aetiologies
- P385 Hypotonic infant with riboflavin transporter deficiency due to slc52a2 mutations
- Homozygous and compound heterozygous mutations in the FBN1 gene: unexpected findings in molecular diagnosis of Marfan syndrome
- SeqHBase: a big data toolset for family based sequencing data analysis
- Bell's palsy syndrome: mimics and chameleons
- A practical approach to the genetic neuropathies
- Treatable Leigh-like encephalopathy presenting in adolescence