[HTML][HTML] Recent advances in amyotrophic lateral sclerosis

N Riva, F Agosta, C Lunetta, M Filippi, A Quattrini - Journal of neurology, 2016 - Springer
ALS is a relentlessly progressive and fatal disease, with no curative therapies available to
date. Symptomatic and palliative care, provided in a multidisciplinary context, still remains …

[PDF][PDF] Amyotrophic lateral sclerosis: from disease mechanisms to therapies

LI Bruijn - Biotechniques, 2002 - 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 …

[HTML][HTML] Amyotrophic lateral sclerosis: a neurodegenerative disorder poised for successful therapeutic translation

RJ Mead, N Shan, HJ Reiser, F Marshall… - Nature Reviews Drug …, 2023 - nature.com
Amyotrophic lateral sclerosis (ALS) is a devastating disease caused by degeneration of
motor neurons. As with all major neurodegenerative disorders, development of disease …

Exploring molecular approaches in amyotrophic lateral sclerosis: drug targets from clinical and pre-clinical findings

M Alam, RK Yadav, E Minj, A Tiwari… - Current Molecular …, 2021 - ingentaconnect.com
Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disease (MND) characterized by
the death of upper and lower motor neurons (corticospinal tract) in the motor cortex, basal …

[HTML][HTML] Translating preclinical insights into effective human trials in ALS

AB DiBernardo, ME Cudkowicz - … et Biophysica Acta (BBA)-Molecular Basis …, 2006 - Elsevier
Amyotrophic lateral sclerosis (ALS) is a rapidly progressive, adult-onset neurodegenerative
disease characterized by selective dysfunction and death of motor neurons in the brain and …

[HTML][HTML] Challenges in the understanding and treatment of amyotrophic lateral sclerosis/motor neuron disease

J Rosenfeld, MJ Strong - Neurotherapeutics, 2015 - Elsevier
With the acceleration in our understanding of ALS and the related motor neuron disease has
come even greater challenges in reconciling all of the proposed pathogenic mechanisms …

How can we improve clinical trials in amyotrophic lateral sclerosis?

PH Gordon, V Meininger - Nature Reviews Neurology, 2011 - nature.com
Since the approval of riluzole for the treatment of amyotrophic lateral sclerosis (ALS) 17
years ago, more than 30 large clinical trials have been conducted, but none has proved …

Amyotrophic lateral sclerosis: new insights into underlying molecular mechanisms and opportunities for therapeutic intervention

M Cozzolino, MG Pesaresi, V Gerbino… - Antioxidants & redox …, 2012 - liebertpub.com
Recent years have witnessed a renewed interest in the pathogenic mechanisms of
amyotrophic lateral sclerosis (ALS), a late-onset progressive degeneration of motor neurons …

Understanding ALS: new therapeutic approaches

A Musarò - The FEBS journal, 2013 - Wiley Online Library
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease associated with
motor neuron degeneration, muscle atrophy and paralysis. Although numerous pathological …

Therapeutic development in amyotrophic lateral sclerosis

M Bucchia, A Ramirez, V Parente, C Simone… - Clinical …, 2015 - Elsevier
Purpose Amyotrophic lateral sclerosis (ALS) is the most common motor neuron disease in
adults. It is almost invariably lethal within a few years after the onset of symptoms. No …