ABSTRACT The occurrence of dementia in amyotrophic lateral sclerosis (ALS) was only widely recognized in the late 20th century. Hitherto, it was believed that dementia was a rare event due to the fortuitous association with other diseases. In 1924, Kostantin Nikolaevich Tretiakoff and Moacyr de Freitas Amorim reported a case of dementia with features of frontotemporal dementia (FTD) that preceded the motor signs of ALS. Neuropathological examination confirmed ALS and found no signs of other dementia-causing diseases. The authors hypothesized that dementia was part of ALS and recommended the search for signs of involvement of motor neurons in cases of dementia with an ill-defined clinical picture, a practice currently accepted in the investi...
This PhD thesis examines the relationship between Amyotrophic Lateral Sclerosis (ALS) and Frontotemp...
The onset of motor symptoms in amyotrophic lateral sclerosis (ALS) is strikingly focal. In three-qua...
Objective: To compare the clinical features at presentation in patients with frontotemporal dementia...
Frontotemporal dementia is a form of presenile dementia, more prevalent in women than in men. In mos...
There is increasing clinical, imaging and neurophatological evidence that Amyotrophic lateral sclero...
The occurrence of cognitive decline in amyotrophic lateral sclerosis (ALS), especially in the form o...
Objective: Primary lateral sclerosis (PLS) is a rare form of motor neuron disease characterised by U...
A 68-year-old man with a clinical diagnosis of Alzheimer’s disease (AD) later developed amyotrophic ...
Amyotrophic lateral sclerosis (ALS) is characterized by degeneration of upper and lower motor neuron...
markdownabstract__Abstract__ In 1892, Arnold Pick described the first patients with a clinical sy...
International audienceAmyotrophic lateral sclerosis (ALS) and frontotemporal dementia have a strong ...
The relationship between motor neurone disease (MND) and frontotemporal dementia (FTD) has been a to...
The concept that frontotemporal dementia (FTD) is a purely cortical dementia has largely been refute...
Cognitive and behavioural impairments accompanying amyotrophic lateral sclerosis (ALS) have been rep...
Cognitive and behavioural impairments accompanying amyotrophic lateral sclerosis (ALS) have been rep...
This PhD thesis examines the relationship between Amyotrophic Lateral Sclerosis (ALS) and Frontotemp...
The onset of motor symptoms in amyotrophic lateral sclerosis (ALS) is strikingly focal. In three-qua...
Objective: To compare the clinical features at presentation in patients with frontotemporal dementia...
Frontotemporal dementia is a form of presenile dementia, more prevalent in women than in men. In mos...
There is increasing clinical, imaging and neurophatological evidence that Amyotrophic lateral sclero...
The occurrence of cognitive decline in amyotrophic lateral sclerosis (ALS), especially in the form o...
Objective: Primary lateral sclerosis (PLS) is a rare form of motor neuron disease characterised by U...
A 68-year-old man with a clinical diagnosis of Alzheimer’s disease (AD) later developed amyotrophic ...
Amyotrophic lateral sclerosis (ALS) is characterized by degeneration of upper and lower motor neuron...
markdownabstract__Abstract__ In 1892, Arnold Pick described the first patients with a clinical sy...
International audienceAmyotrophic lateral sclerosis (ALS) and frontotemporal dementia have a strong ...
The relationship between motor neurone disease (MND) and frontotemporal dementia (FTD) has been a to...
The concept that frontotemporal dementia (FTD) is a purely cortical dementia has largely been refute...
Cognitive and behavioural impairments accompanying amyotrophic lateral sclerosis (ALS) have been rep...
Cognitive and behavioural impairments accompanying amyotrophic lateral sclerosis (ALS) have been rep...
This PhD thesis examines the relationship between Amyotrophic Lateral Sclerosis (ALS) and Frontotemp...
The onset of motor symptoms in amyotrophic lateral sclerosis (ALS) is strikingly focal. In three-qua...
Objective: To compare the clinical features at presentation in patients with frontotemporal dementia...