Article info
PDFNeurological rarities
Niemann–Pick type C: a potentially treatable disorder?
- Correspondence to Professor Marios Hadjivassiliou, Academic Department of Neurosciences, Royal Hallamshire Hospital, Glossop Rd, Sheffield S10 2JF, UK; m.hadjivassiliou{at}sheffield.ac.uk
Citation
Niemann–Pick type C: a potentially treatable disorder?
Publication history
- First published August 1, 2013.
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
- Niemann-Pick type C: contemporary diagnosis and treatment of a classical disorder
- Patient with Niemann-Pick disease type C: over 20 years' follow-up
- Niemann-Pick disease type C or Gaucher’s disease type 3? A clinical conundrum
- Six novel NPC1 mutations in Chinese patients with Niemann–Pick disease type C
- Complications associated with intrathecal drug delivery in a paediatric patient with Niemann-Pick type C
- Intrathecal cyclodextrin in the treatment of Niemann-Pick disease type C
- Niemann–Pick type C disease in a 68-year-old patient
- Claustrum hyperintensity: a rare radiological correlate in Niemann-Pick disease
- Proton magnetic resonance spectroscopic imaging in the clinical evaluation of patients with Niemann-Pick type C disease
- Isolated splenomegaly as the presenting feature of Niemann–Pick disease type C