Prevalence, characteristics, and survival of frontotemporal lobar degeneration syndromes

@inproceedings{CoyleGilchrist2016PrevalenceCA,
  title={Prevalence, characteristics, and survival of frontotemporal lobar degeneration syndromes},
  author={Ian T. S. Coyle-Gilchrist and Katrina M. Dick and Karalyn Patterson and Patricia V{\'a}zquez Rodr{\'i}quez and Eileen Wehmann and Alicia Wilcox and Claire J. Lansdall and Kate E. Dawson and Julie Wiggins and Simon Mead and Carol Brayne and James B. Rowe},
  booktitle={Neurology},
  year={2016}
}
OBJECTIVES To estimate the lifetime risk, prevalence, incidence, and mortality of the principal clinical syndromes associated with frontotemporal lobar degeneration (FTLD) using revised diagnostic criteria and including intermediate clinical phenotypes. METHODS Multisource referral over 2 years to identify all diagnosed or suspected cases of frontotemporal dementia (FTD), progressive supranuclear palsy (PSP), or corticobasal syndrome (CBS) in 2 UK counties (population 1.69 million… CONTINUE READING
Recent Discussions
This paper has been referenced on Twitter 5 times over the past 90 days. VIEW TWEETS
24 Citations
38 References
Similar Papers

Citations

Publications citing this paper.
Showing 1-10 of 24 extracted citations

References

Publications referenced by this paper.
Showing 1-10 of 38 references

Characteristics of progressive supranuclear palsy presenting with corticobasal syndrome: a cortical variant

  • H Ling, R de Silva
  • Neuropathol Appl Neurobiol
  • 2014
Highly Influential
4 Excerpts

Similar Papers

Loading similar papers…