Amyotrophic lateral sclerosis-frontotemporal spectrum disorder (ALS-FTSD): Revised diagnostic criteria

MJ Strong, S Abrahams, LH Goldstein… - … lateral sclerosis and …, 2017 - Taylor & Francis
This article presents the revised consensus criteria for the diagnosis of frontotemporal
dysfunction in amyotrophic lateral sclerosis (ALS) based on an international research …

The role of noradrenaline in cognition and cognitive disorders

N Holland, TW Robbins, JB Rowe - Brain, 2021 - academic.oup.com
Many aspects of cognition and behaviour are regulated by noradrenergic projections to the
forebrain originating from the locus coeruleus, acting through alpha and beta …

Revised Airlie House consensus guidelines for design and implementation of ALS clinical trials

LH Van Den Berg, E Sorenson, G Gronseth… - Neurology, 2019 - AAN Enterprises
Objective To revise the 1999 Airlie House consensus guidelines for the design and
implementation of preclinical therapeutic studies and clinical trials in amyotrophic lateral …

[HTML][HTML] Cognitive, emotional and psychological manifestations in amyotrophic lateral sclerosis at baseline and overtime: a review

S Benbrika, B Desgranges, F Eustache… - Frontiers in …, 2019 - frontiersin.org
It is now well recognized that, in addition to motor impairment, amyotrophic lateral sclerosis
(ALS) may cause extra-motor clinical signs and symptoms. These can include the alteration …

Motor neuron disease: pathophysiology, diagnosis, and management

LA Foster, MK Salajegheh - The American journal of medicine, 2019 - Elsevier
Patients with motor neuron diseases may present to primary care clinic or may be initially
encountered in the inpatient setting. Timely diagnosis of these conditions is a key factor in …

Neuropsychological impairment in amyotrophic lateral sclerosis–frontotemporal spectrum disorder

S Abrahams - Nature Reviews Neurology, 2023 - nature.com
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease with a rapid course,
characterized by motor neuron dysfunction, leading to progressive disability and death. This …

[HTML][HTML] Qualitative measures that assess functional disability and quality of life in ALS

SL Hartmaier, T Rhodes, SF Cook, C Schlusser… - Health and quality of life …, 2022 - Springer
Background Selection of appropriate trial endpoints and outcome measures is particularly
important in rare disease and rapidly progressing disease such as amyotrophic lateral …

[HTML][HTML] Psychiatric symptoms in amyotrophic lateral sclerosis: beyond a motor neuron disorder

E Zucchi, N Ticozzi, J Mandrioli - Frontiers in neuroscience, 2019 - frontiersin.org
The historical view that Amyotrophic Lateral Sclerosis (ALS) as a pure motor disorder has
been increasingly challenged by the discovery of cognitive and behavioral changes in the …

[HTML][HTML] The spectrum of cognitive dysfunction in amyotrophic lateral sclerosis: an update

KA Jellinger - International Journal of Molecular Sciences, 2023 - mdpi.com
Cognitive dysfunction is an important non-motor symptom in amyotrophic lateral sclerosis
(ALS) that has a negative impact on survival and caregiver burden. It shows a wide spectrum …

[HTML][HTML] Communication matters—pitfalls and promise of hightech communication devices in palliative care of severely physically disabled patients with amyotrophic …

K Linse, E Aust, M Joos, A Hermann - Frontiers in neurology, 2018 - frontiersin.org
Amyotrophic lateral sclerosis (ALS) is the most common motor neuron disease, leading to
progressive paralysis, dysarthria, dysphagia, and respiratory disabilities. Therapy is mostly …