Article info
PDFEditorial
Not just neurological stamp collecting: when rare diagnoses lead to fundamental advances
- Correspondence to Professor Jonathan M Schott, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK; j.schott{at}ucl.ac.uk
Citation
Not just neurological stamp collecting: when rare diagnoses lead to fundamental advances
Online issue publication
October 18, 2023
Article Versions
- Previous version (18 October 2023).
- 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)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.
Other content recommended for you
- A rare cause of young-onset dementia
- Convergent molecular defects underpin diverse neurodegenerative diseases
- Genetics insight into the amyotrophic lateral sclerosis/frontotemporal dementia spectrum
- Frontotemporal dementia presentation in patients with heterozygous p.H157Y variant of TREM2
- Comparison of the pattern of atrophy of the corpus callosum in frontotemporal dementia, progressive supranuclear palsy, and Alzheimer's disease
- Cerebellar atrophy in neurodegeneration—a meta-analysis
- Neurofilament light chain in serum for the diagnosis of amyotrophic lateral sclerosis
- Neurofilament light chain as a biomarker in neurological disorders
- 31st Advanced Clinical Neurology Course, Edinburgh 2009: progressive cognitive impairment, behavioural change and upper motor neuron signs in a 57-year-old woman
- Fluid biomarkers in frontotemporal dementia: past, present and future