Evaluation of the application of the European guidelines for the diagnosis and clinical care of amyotrophic lateral sclerosis (ALS) patients in six French ALS centres
Background and purpose Our objective was to evaluate the extent to which the 2005
recommendations of the European Federation of Neurological Sciences (EFNS) on the …
recommendations of the European Federation of Neurological Sciences (EFNS) on the …
Amyotrophic lateral sclerosis (motor neuron disease): proposed mechanisms and pathways to treatment
EF Goodall, KE Morrison - Expert reviews in molecular medicine, 2006 - cambridge.org
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterised by
loss of motor neurons. The cause of disease is unknown other than in the rare cases of …
loss of motor neurons. The cause of disease is unknown other than in the rare cases of …
Therapeutic targets in amyotrophic lateral sclerosis: focus on ion channels and skeletal muscle
N Tarantino, I Canfora, GM Camerino, S Pierno - Cells, 2022 - mdpi.com
Amyotrophic Lateral Sclerosis is a neurodegenerative disease caused by progressive loss
of motor neurons, which severely compromises skeletal muscle function. Evidence shows …
of motor neurons, which severely compromises skeletal muscle function. Evidence shows …
[PDF][PDF] Amyotrophic lateral sclerosis: from disease mechanisms to therapies
LI Bruijn - Biotechniques, 2024 - Taylor & Francis
Amyotrophic lateral sclerosis (ALS) or Lou Gehrig's disease is the most common motor
neuron disease in human adults, described as early as 1869 by a French neurobiologist and …
neuron disease in human adults, described as early as 1869 by a French neurobiologist and …
[PDF][PDF] Practice advisory on the treatment of amyotrophic lateral sclerosis with riluzole: Report of the Quality Standards Subcommittee of the American Academy of …
Quality Standards Subcommittee of the American … - Neurology, 1997 - AAN Enterprises
with bulbar onset, 35% of placebo-treated patients were still alive compared with 73% of
riluzoletreated patients; whereas for the limb-onset patients, 64% of placebo-treated patients …
riluzoletreated patients; whereas for the limb-onset patients, 64% of placebo-treated patients …
Dose-ranging study of riluzole in amyotrophic lateral sclerosis
RS Group II, L Lacomblez, G Bensimon, V Meininger… - The Lancet, 1996 - Elsevier
BackgroundAmyotrophic lateral sclerosis (ALS) is a progressive disease with no effective
treatment. In an initial study, riluzole decreased mortality and slowed muscle-strength …
treatment. In an initial study, riluzole decreased mortality and slowed muscle-strength …
Diagnostic investigation and multidisciplinary management in motor neuron disease
JA Rocha, C Reis, F Simoes, J Fonseca… - Journal of …, 2005 - Springer
Amyotrophic lateral sclerosis (ALS) is the most common adult-onset motor neuron disease.
ALS is a progressive neurodegenerative disorder, involving motor neurons in the cerebral …
ALS is a progressive neurodegenerative disorder, involving motor neurons in the cerebral …
Riluzole and amyotrophic lateral sclerosis survival: a population‐based study in southern Italy
S Zoccolella, E Beghi, G Palagano… - European journal of …, 2007 - Wiley Online Library
Riluzole is to date the only treatment that prolongs amyotrophic lateral sclerosis (ALS)
survival. However, results on the efficacy of riluzole in observational population‐based …
survival. However, results on the efficacy of riluzole in observational population‐based …
Introduction to supplement: The current status of treatment for ALS
RG Miller, SH Appel - Amyotrophic Lateral Sclerosis and …, 2017 - Taylor & Francis
ALS is a lethal neurodegenerative disease wherein the diagnosis is often delayed. Our
understanding of the pathobiology is slowly expanding, and the number of new genes is …
understanding of the pathobiology is slowly expanding, and the number of new genes is …