[HTML][HTML] Clinical measures of bulbar dysfunction in ALS

Y Yunusova, EK Plowman, JR Green, C Barnett… - Frontiers in …, 2019 - frontiersin.org
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 …

[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 …

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 …

[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 …

[HTML][HTML] Temporal stratification of amyotrophic lateral sclerosis patients using disease progression patterns

D M. Amaral, DF Soares, M Gromicho… - Nature …, 2024 - nature.com
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 …

[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 …

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 …

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 …

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 …

[HTML][HTML] Leveraging process mining for modeling progression trajectories in amyotrophic lateral sclerosis

E Tavazzi, R Gatta, M Vallati, S Cotti Piccinelli… - BMC Medical Informatics …, 2022 - Springer
Abstract Background Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative disease
whose spreading and progression mechanisms are still unclear. The ability to predict ALS …