Chronic inhibitory effect of riluzole on trophic factor production
CN Dennys, JN Armstrong, M Levy, YJ Byun… - Experimental …, 2015 - Elsevier
Riluzole is the only FDA approved drug for the treatment of amyotrophic lateral sclerosis
(ALS). However, the drug affords moderate protection to ALS patients, extending life for a …
(ALS). However, the drug affords moderate protection to ALS patients, extending life for a …
Current clinical trials in amyotrophic lateral sclerosis
JM Bhatt, PH Gordon - Expert Opinion on Investigational Drugs, 2007 - Taylor & Francis
Amyotrophic lateral sclerosis is caused by selective degeneration of motor neurons in the
brain and spinal cord. There are still no other effective therapies 10 years after the approval …
brain and spinal cord. There are still no other effective therapies 10 years after the approval …
Amyotrophic lateral sclerosis: pathophysiology, diagnosis and management
PH Gordon - CNS drugs, 2011 - Springer
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease associated
with a life expectancy of approximately 3 years after symptom onset, but the range of survival …
with a life expectancy of approximately 3 years after symptom onset, but the range of survival …
New therapy options for amyotrophic lateral sclerosis
P Gordon, P Corcia, V Meininger - Expert opinion on …, 2013 - Taylor & Francis
Introduction: Amyotrophic lateral sclerosis (ALS) is a rapidly progressing neurodegenerative
disease leading almost irrevocably to paralysis and death within 5 years after the first …
disease leading almost irrevocably to paralysis and death within 5 years after the first …
Als and Ftd: Insights into the disease mechanisms and therapeutic targets
RM Liscic - European Journal of Pharmacology, 2017 - Elsevier
Amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) are
neurodegenerative disorders, related by signs of deteriorating motor and cognitive functions …
neurodegenerative disorders, related by signs of deteriorating motor and cognitive functions …
Efficacy and safety of xaliproden in amyotrophic lateral sclerosis: results of two phase III trials
V Meininger, G Bensimon, WG Bradley… - … lateral sclerosis and …, 2004 - Taylor & Francis
Amyotrophic lateral sclerosis (ALS) is a relentlessly progressive and fatal motor neuron
disease. We carried out two randomized, double‐blind, placebo‐controlled, multi‐centre …
disease. We carried out two randomized, double‐blind, placebo‐controlled, multi‐centre …
Amyotrophic lateral sclerosis risk genes and suppressor
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that leads to death
by progressive paralysis and respiratory failure within 2-4 years of onset. About 90-95% of …
by progressive paralysis and respiratory failure within 2-4 years of onset. About 90-95% of …
Old versus New Mechanisms in the Pathogenesis of ALS
S Rossi, M Cozzolino, MT Carrì - Brain pathology, 2016 - Wiley Online Library
Abstract Amyotrophic Lateral Sclerosis (ALS) is recognized as a very complex disease. As
we have learned in the past 20 years from studies in patients and in models based on the …
we have learned in the past 20 years from studies in patients and in models based on the …
A review of the neural mechanisms of action and clinical efficiency of riluzole in treating amyotrophic lateral sclerosis: what have we learned in the last decade?
MC Bellingham - CNS neuroscience & therapeutics, 2011 - Wiley Online Library
Amyotrophic lateral sclerosis (ALS) is a devastating and fatal neurodegenerative disease of
adults which preferentially attacks the neuromotor system. Riluzole has been used as the …
adults which preferentially attacks the neuromotor system. Riluzole has been used as the …
Riluzole for ALS: what is the evidence?
R Miller - Amyotrophic Lateral Sclerosis and Other Motor Neuron …, 2003 - Taylor & Francis
It has been eight years since the Food and Drug Administration approved riluzole as the
only drug of established value in slowing disease progression for patients with ALS. The …
only drug of established value in slowing disease progression for patients with ALS. The …