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 Concept Videos

Alzheimer's Disease: Treatment01:22

Alzheimer's Disease: Treatment

Alzheimer's Disease (AD), a neurodegenerative disorder, is pathologically identified by amyloid plaques and neurofibrillary tangles composed of tau protein. AD pharmacotherapy aims to manage cognitive symptoms, delay disease progression, and treat behavioral symptoms. The treatment is primarily symptomatic and palliative, with no definitive disease-modifying therapy available. Cholinesterase inhibitors, including donepezil (Aricept), rivastigmine (Exelon), and galantamine (Razadyne), are...
Dementia l: Introduction01:22

Dementia l: Introduction

Dementia is an acquired, progressive syndrome characterized by a decline in multiple cognitive domains severe enough to impair daily functioning and reduce independence. Although memory loss is a central feature, the diagnosis requires additional deficits involving language, executive function, visuospatial skills, judgment, calculation, or abstract reasoning. These cognitive impairments reflect underlying neurodegenerative or vascular processes that gradually disrupt neuronal networks...
Alzheimer's Disease: Overview01:26

Alzheimer's Disease: Overview

Alzheimer's Disease (AD) is a continually advancing neurodegenerative disorder, distinguished by escalating memory loss, cognitive dysfunction, and dementia. The disease unfolds in three stages: preclinical, mild cognitive impairment (MCI), and dementia. Its onset is insidious, and the progression gradual, with the cause not well explained by other disorders.
The clinical diagnosis of AD hinges on the presence of memory and other cognitive impairments. Biomarkers, such as changes in Aβ and tau...
Alzheimer Disease ll: Pathophysiology01:23

Alzheimer Disease ll: Pathophysiology

Alzheimer disease involves structural changes in the brain that begin long before symptoms appear. The most distinctive features are extracellular neuritic plaques and intracellular neurofibrillary tangles.Neuritic plaques form in the cerebral cortex and around blood vessels. These plaques contain a dense core of beta-amyloid (Aβ)—a toxic protein fragment that clumps outside neurons. The core is surrounded by damaged neuronal extensions, as well as reactive astrocytes and microglia. Abnormal...
Alzheimer Disease l: Introduction01:29

Alzheimer Disease l: Introduction

Alzheimer disease is a chronic, progressive, and irreversible neurodegenerative disorder and the most common cause of dementia in older adults. It leads to gradual neuronal loss, causing cognitive decline, behavioral changes, and loss of functional independence.Risk Factors and EtiologyThe disease is multifactorial. Age is the strongest risk factor, with prevalence doubling every 5 years after age 65. Genetic factors include mutations in genes such as APP, PSEN1, and PSEN2, which are associated...
Dementia01:30

Dementia

Dementia is a collective term for cognitive disorders primarily affecting memory, thinking, and reasoning. It is not a specific disease but a syndrome, with Alzheimer's disease being the most common cause, accounting for approximately 60-80% of cases. Other types include vascular dementia, Lewy body dementia, and frontotemporal dementia. Dementia affects millions worldwide, particularly older adults, though it is not a normal part of aging.
The progression of dementia is generally gradual.

You might also read

Related Articles

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

Sort by
Same author

Clinicopathologic features and results of transcatheter arterial chemoembolization for osteosarcoma.

Cardiovascular and interventional radiology·2007
Same author

[The clinical significance of expression and amplification of FGF3 in bladder transitional cell carcinoma].

Zhonghua yi xue za zhi·2007
Same author

Efficient in vivo 31P magnetization transfer approach for noninvasively determining multiple kinetic parameters and metabolic fluxes of ATP metabolism in the human brain.

Magnetic resonance in medicine·2006
Same author

Tuning the hole injection barrier at the organic/metal interface with self-assembled functionalized aromatic thiols.

The journal of physical chemistry. B·2006
Same author

Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation.

European journal of human genetics : EJHG·2006
Same author

[Characterization of hydrogen peroxide production by a novel oral streptococci, S. oligofermentans isolated from human oral cavity].

Wei sheng wu xue bao = Acta microbiologica Sinica·2006
Same journal

Treatment of Clinically Diagnosed Alzheimer's Disease by External Counterpulsation A Randomized Clinical Trial.

American journal of Alzheimer's disease and other dementias·2026
Same journal

Community-Based Physician Attitudes Related to the Diagnosis and Treatment of Early Alzheimer's Disease in the United States.

American journal of Alzheimer's disease and other dementias·2026
Same journal

Daily Living, Depressive Symptoms, and Cognition in Older Adults With Chronic Diseases.

American journal of Alzheimer's disease and other dementias·2026
Same journal

Four Common Beliefs About Patient Memory Evaluations: Who Has Them and What Modifies Them?

American journal of Alzheimer's disease and other dementias·2026
Same journal

The Changes of Quality of Life, Behavioural Problems, and Cognition Among Older Adults With Severe Dementia Under Social Distancing Measures in Residential Homes.

American journal of Alzheimer's disease and other dementias·2026
Same journal

Validating the Use of TBI-CareQOL Measures in Caregivers of People Living With Dementia.

American journal of Alzheimer's disease and other dementias·2026
See all related articles

Related Experiment Video

Updated: May 16, 2026

Abbiategrasso Brain Bank Protocol for Collecting, Processing and Characterizing Aging Brains
12:28

Abbiategrasso Brain Bank Protocol for Collecting, Processing and Characterizing Aging Brains

Published on: June 3, 2020

Progress in frontotemporal dementia research.

Xinling Wang1, Yuedi Shen, Wei Chen

  • 1Department of Psychiatry, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.

American Journal of Alzheimer'S Disease and Other Dementias
|December 11, 2012
PubMed
Summary
This summary is machine-generated.

Frontotemporal dementia (FTD) is a common presenile dementia. Understanding its pathogenesis and utilizing animal models are key to developing new therapies for FTD.

More Related Videos

Fluorescence-Activated Cell Sorting-Radioligand Treated Tissue (FACS-RTT) to Determine the Cellular Origin of Radioactive Signal
12:04

Fluorescence-Activated Cell Sorting-Radioligand Treated Tissue (FACS-RTT) to Determine the Cellular Origin of Radioactive Signal

Published on: September 10, 2021

Related Experiment Videos

Last Updated: May 16, 2026

Abbiategrasso Brain Bank Protocol for Collecting, Processing and Characterizing Aging Brains
12:28

Abbiategrasso Brain Bank Protocol for Collecting, Processing and Characterizing Aging Brains

Published on: June 3, 2020

Fluorescence-Activated Cell Sorting-Radioligand Treated Tissue (FACS-RTT) to Determine the Cellular Origin of Radioactive Signal
12:04

Fluorescence-Activated Cell Sorting-Radioligand Treated Tissue (FACS-RTT) to Determine the Cellular Origin of Radioactive Signal

Published on: September 10, 2021

Area of Science:

  • Neuroscience
  • Neurology
  • Pathology

Background:

  • Frontotemporal dementia (FTD) is the second most common presenile dementia, typically emerging before age 60.
  • FTD presents with behavioral, affective, and language impairments, stemming from a genetically and pathologically diverse degenerative disorder.
  • Current FDA-approved treatments specifically for FTD are lacking.

Purpose of the Study:

  • To review recent advancements in the molecular pathogenesis, pathology, and therapeutic strategies for FTD.
  • To highlight the role of animal models in understanding FTD's mechanisms.
  • To identify potential new therapeutic targets for FTD.

Main Methods:

  • Literature review of recent research on FTD.
  • Analysis of studies focusing on molecular pathogenesis and pathology.
  • Examination of findings from animal models of FTD.
  • Review of current and emerging therapeutic approaches.

Main Results:

  • FTD is characterized by significant heterogeneity in genetics and pathology.
  • Animal models offer valuable insights into the underlying pathogenic mechanisms of FTD.
  • No specific FDA-approved medications currently exist for FTD treatment.

Conclusions:

  • A deeper comprehension of FTD pathogenesis is crucial for therapeutic development.
  • Animal models are instrumental in advancing our understanding and identifying therapeutic targets for FTD.
  • Future research focusing on pathogenesis and animal models will drive novel treatment strategies for FTD.