Increased awareness of cognitive and behavioural change in amyotrophic lateral sclerosis
has been driven by various clinic-based and population-based studies. A frontotemporal …

Advances in neuroimaging, complementing histopathological insights, have established a
multi-system involvement of cerebral networks beyond the traditional neuromuscular …

Amyotrophic lateral sclerosis (ALS) is the most common motor neuron disease, leading to
progressive paralysis, dysarthria, dysphagia, and respiratory disabilities. Therapy is mostly …

A relative preservation of eye movements is notable in ALS, but saccadic functions have not
been studied longitudinally. ALS overlaps with FTD, typically involving executive …

There is strong clinical, imaging and pathological evidence that neurodegeneration is
associated with altered brain connectivity. While functional imaging (fMRI) can detect resting …

Objective: We examined narrative discourse in amyotrophic lateral sclerosis (ALS) to assess
the role of executive functioning in support of language and the neuroanatomical basis for …

The paper presents some speculations on the loss of voluntary responses and operant
learning in long-term paralysis in human patients and curarized rats. Based on a …

Objective: Amyotrophic lateral sclerosis (ALS) is a complex neurodegenerative disease that
causes the progressive loss of voluntary muscle control. Recent studies have reported …

Objective: Executive dysfunctions in patients suffering from amyotrophic lateral sclerosis
(ALS) are often described but poorly understood. Specifically, research on patients' ability to …

Cognitive impairment in amyotrophic lateral sclerosis (ALS) is heterogeneous but now
recognized as a feature in non-demented patients and no longer exclusively attributed to …