Objective: To investigate and compare two ALS staging systems, King’s clinical staging and Milano-Torino (MiToS) functional staging, using data from the LiCALS phase III clinical trial (EudraCT 2008-006891-31). Methods: Disease stage was derived retrospectively for each system from the ALS Functional Rating Scale-Revised subscores using standard methods. The two staging methods were then compared for timing of stages using box plots, correspondence using chi-square tests, agreement using a linearly weighted kappa coefficient and concordance using Spearman’s rank correlation. Results: For both systems, progressively higher stages occurred at progressively later proportions of the disease course, but the distribution differed between the two ...
Objective: Clinical stages in amyotrophic lateral sclerosis (ALS) can be measured using a simple sys...
Objective: The choice of adequate proxy for long-term survival, the ultimate outcome in randomised c...
Objectives: Propose an empirical amyotrophic lateral sclerosis (ALS) staging approach called Fine’ti...
To investigate and compare two ALS staging systems, King's clinical staging and Milano-Torino (MiToS...
Background: Amyotrophic lateral sclerosis (ALS) shows considerable clinical heterogeneity, which aff...
OBJECTIVE: To evaluate the Milano-Torino staging (MiToS) and King\u27s staging systems as potential ...
International audienceBackground: Assessing clinical progression in amyotrophic lateral sclerosis (A...
Background: Amyotrophic lateral sclerosis (ALS) shows considerable clinical heterogeneity, which aff...
Background and purpose: To compare two recently developed staging systems for amyotrophic lateral sc...
OBJECTIVE: Clinical stages in amyotrophic lateral sclerosis (ALS) can be measured using a simple sys...
Objective: It is important to explore the utility of clinical staging systems in the management of a...
International audienceAbstractAmyotrophic lateral sclerosis (ALS) is a heterogenous motoneuronal neu...
Objective: Clinical stages in amyotrophic lateral sclerosis (ALS) can be measured using a simple sys...
Objective: The choice of adequate proxy for long-term survival, the ultimate outcome in randomised c...
Objectives: Propose an empirical amyotrophic lateral sclerosis (ALS) staging approach called Fine’ti...
To investigate and compare two ALS staging systems, King's clinical staging and Milano-Torino (MiToS...
Background: Amyotrophic lateral sclerosis (ALS) shows considerable clinical heterogeneity, which aff...
OBJECTIVE: To evaluate the Milano-Torino staging (MiToS) and King\u27s staging systems as potential ...
International audienceBackground: Assessing clinical progression in amyotrophic lateral sclerosis (A...
Background: Amyotrophic lateral sclerosis (ALS) shows considerable clinical heterogeneity, which aff...
Background and purpose: To compare two recently developed staging systems for amyotrophic lateral sc...
OBJECTIVE: Clinical stages in amyotrophic lateral sclerosis (ALS) can be measured using a simple sys...
Objective: It is important to explore the utility of clinical staging systems in the management of a...
International audienceAbstractAmyotrophic lateral sclerosis (ALS) is a heterogenous motoneuronal neu...
Objective: Clinical stages in amyotrophic lateral sclerosis (ALS) can be measured using a simple sys...
Objective: The choice of adequate proxy for long-term survival, the ultimate outcome in randomised c...
Objectives: Propose an empirical amyotrophic lateral sclerosis (ALS) staging approach called Fine’ti...