genetic and molecular bases of neurodegenerative disorders have led to a shift away from traditional nomenclatures of clinical syndromes. Historically, frontotemporal lobar degeneration (FTLD ...

At least 18 different disorders can be distinguished on pathological and genetic grounds ... prominent apraxia (corticobasal degeneration), parkinsonism (frontotemporal lobar degeneration ...

The company anticipates topline data from the Phase 3 INFRONT-3 trial of latozinemab for frontotemporal dementia ... Leveraging the principles of genetics, immunology and neuroscience, the company ...

Frontotemporal dementia (FTD ... and language due to degeneration in the frontal and temporal lobes of the brain. Amyotrophic lateral sclerosis (ALS), the most common degenerative motor neuron ...

Delve into the increasingly dynamic landscape of ALS treatment development with thirteen companies advancing candidates in ...

Gaps remain in biomedical research in frontotemporal dementia; however, there are several means by which these gaps can be bridged.

On the surface, the movement disorder amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, and the cognitive disorder frontotemporal lobar degeneration (FTLD), which underlies ...

Frontotemporal dementia (FTD) can be hard to diagnose, because it is an uncommon type of dementia and does not cause memory problems at first. However, there are some ways to diagnose FTD including ...

The research, published in the Journal of Genetic Counseling, interviewed 13 people—both parents and non-parents—who are at risk of developing familial frontotemporal dementia (fFTD).

The research, published in the Journal of Genetic Counselling, interviewed 13 people – both parents and non-parents – who are at risk of developing familial frontotemporal dementia (fFTD). “Our study ...