Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Frontotemporal dementia.

David Neary1, Julie Snowden, David Mann

  • 1Clinical Neuroscience Group, Hope Hospital, Salford, Greater Manchester M6 8HD, UK. david.neary@manchester.ac.uk

The Lancet. Neurology
|October 22, 2005
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Are Lung Allografts From Drug Overdose Deaths Safe to Use for Transplantation? A Nationwide Analysis.

Annals of thoracic surgery short reports·2026
Same author

Interpersonal interactions improve the representativeness of embodied decision-making behaviour in football.

Psychology of sport and exercise·2026
Same author

Clinical recognition of frontotemporal dementia with right temporal predominance: a consensus statement from the International Working Group.

Communications medicine·2025
Same author

Algorithmic gaze annotation for mobile eye-tracking.

Behavior research methods·2025
Same author

Technical Advances and Outcomes of Fetal Atrial Septal Intervention for Restrictive or Intact Atrial Septum.

Circulation. Cardiovascular interventions·2025
Same author

Introduction of the transmissible mobile colistin resistance genes <i>mcr-3</i> and <i>mcr-9</i> to the USA via imported seafood.

mSphere·2025
Same journal

Resolution of expression of concern-Serotonergic pathology and disease burden in the premotor and motor phase of A53T α-synuclein parkinsonism: a cross-sectional study.

The Lancet. Neurology·2026
Same journal

UCL Queen Square Institute of Neurology: 75 years of innovation.

The Lancet. Neurology·2026
Same journal

Correction to Lancet Neurol 2026; 25: 631.

The Lancet. Neurology·2026
Same journal

Epstein-Barr virus and multiple sclerosis: from associations to mechanisms to potential therapies.

The Lancet. Neurology·2026
Same journal

Correction to Lancet Neurol 2025; 24: 740-52.

The Lancet. Neurology·2026
Same journal

Correction to Lancet Neurol 2026; 25: 357-67.

The Lancet. Neurology·2026
See all related articles

Frontotemporal dementia (FTD) is a brain disorder affecting personality and behavior due to prefrontal and temporal cortex degeneration. Its diverse causes, including tau protein abnormalities and genetic mutations, present diagnostic and research challenges.

Area of Science:

  • Neuroscience
  • Neurology
  • Pathology

Background:

  • Frontotemporal dementia (FTD) is a clinical syndrome marked by personality and social conduct changes.
  • It involves degeneration of the prefrontal and anterior temporal cortex, typically with onset in middle age and an 8-year survival rate.
  • FTD shares pathological links with tauopathies like progressive supranuclear palsy and corticobasal degeneration due to microtubule-associated protein tau features and tau gene mutations in some cases.

Purpose of the Study:

  • To explore the pathological and etiological heterogeneity of Frontotemporal Dementia.
  • To understand the neurobiological basis of FTD.
  • To address the challenges in clinical management and theoretical understanding of FTD.

Main Methods:

  • Clinical characterization of FTD patients.

Related Experiment Videos

  • Pathological examination focusing on tau protein and tau gene.
  • Genetic analysis of familial FTD cases.
  • Main Results:

    • Over half of FTD patients, including those with family history, lack apparent tau gene or protein abnormalities.
    • This indicates significant pathological and etiological heterogeneity in FTD.
    • Some familial cases show tau gene mutations, linking FTD to other tauopathies.

    Conclusions:

    • FTD is a heterogeneous disorder with diverse underlying pathologies and causes.
    • The role of tau protein is significant in some FTD cases but not all.
    • Further research is needed to fully understand the neurobiology and improve management of FTD.