[HTML][HTML] Clinical measures of bulbar dysfunction in ALS
Bulbar impairment represents a hallmark feature of Amyotrophic Lateral Sclerosis (ALS) that
significantly impacts survival and quality of life. Speech and swallowing dysfunction are key …
significantly impacts survival and quality of life. Speech and swallowing dysfunction are key …
[HTML][HTML] Machine learning in amyotrophic lateral sclerosis: achievements, pitfalls, and future directions
V Grollemund, PF Pradat, G Querin, F Delbot… - Frontiers in …, 2019 - frontiersin.org
Background: Amyotrophic Lateral Sclerosis (ALS) is a relentlessly progressive
neurodegenerative condition with limited therapeutic options at present. Survival from …
neurodegenerative condition with limited therapeutic options at present. Survival from …
An old friend who has overstayed their welcome: the ALSFRS-R total score as primary endpoint for ALS clinical trials
RPA van Eijk, AD de Jongh… - … Lateral Sclerosis and …, 2021 - Taylor & Francis
Abstract Objective: The ALSFRS-R is limited by multidimensionality, which originates from
the summation of various subscales. This prevents a direct comparison between patients …
the summation of various subscales. This prevents a direct comparison between patients …
[HTML][HTML] Tracking a fast-moving disease: longitudinal markers, monitoring, and clinical trial endpoints in ALS
RH Chipika, E Finegan, S Li Hi Shing… - Frontiers in …, 2019 - frontiersin.org
Amyotrophic lateral sclerosis (ALS) encompasses a heterogeneous group of phenotypes
with different progression rates, varying degree of extra-motor involvement and divergent …
with different progression rates, varying degree of extra-motor involvement and divergent …
[HTML][HTML] Temporal stratification of amyotrophic lateral sclerosis patients using disease progression patterns
Identifying groups of patients with similar disease progression patterns is key to understand
disease heterogeneity, guide clinical decisions and improve patient care. In this paper, we …
disease heterogeneity, guide clinical decisions and improve patient care. In this paper, we …
[HTML][HTML] Umbilical cord mesenchymal stem cells in amyotrophic lateral sclerosis: an original study
M Barczewska, S Maksymowicz… - Stem Cell Reviews and …, 2020 - Springer
Objective Amyotrophic lateral sclerosis (ALS) is still incurable. Although different therapies
can affect the health and survival of patients. Our aim is to evaluate the effect of umbilical …
can affect the health and survival of patients. Our aim is to evaluate the effect of umbilical …
The future of ALS diagnosis and staging: where do we go from here?
A Genge, A Chio - Amyotrophic Lateral Sclerosis and …, 2023 - Taylor & Francis
Amyotrophic lateral sclerosis (ALS) is a rare, progressive multi-system neurodegenerative
disorder. Its clinical presentation varies considerably leading to delays in diagnosis, which …
disorder. Its clinical presentation varies considerably leading to delays in diagnosis, which …
Manifold learning for amyotrophic lateral sclerosis functional loss assessment: Development and validation of a prognosis model
V Grollemund, G Le Chat, MS Secchi-Buhour… - Journal of …, 2021 - Springer
Amyotrophic lateral sclerosis (ALS) is an inexorably progressive neurodegenerative
condition with no effective disease-modifying therapy at present. Given the striking clinical …
condition with no effective disease-modifying therapy at present. Given the striking clinical …
Radicava (edaravone) for amyotrophic lateral sclerosis: US experience at 1 year after launch
C Jackson, T Heiman-Patterson, P Kittrell… - … Lateral Sclerosis and …, 2019 - Taylor & Francis
Abstract Background: Radicava®(edaravone), approved for the treatment of amyotrophic
lateral sclerosis (ALS) in 2017, may be administered intravenously at clinic sites, infusion …
lateral sclerosis (ALS) in 2017, may be administered intravenously at clinic sites, infusion …
[HTML][HTML] Leveraging process mining for modeling progression trajectories in amyotrophic lateral sclerosis
Abstract Background Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative disease
whose spreading and progression mechanisms are still unclear. The ability to predict ALS …
whose spreading and progression mechanisms are still unclear. The ability to predict ALS …