Riluzole for amyotrophic lateral sclerosis (ALS)/motor neuron disease (MND)

RG Miller, DH Moore - Cochrane database of systematic …, 2012 - cochranelibrary.com
Background Riluzole is approved for the treatment of amyotrophic lateral sclerosis in most
countries. Questions persist about its clinical utility because of high cost and modest efficacy …

Practice parameter: the care of the patient with amyotrophic lateral sclerosis (an evidence-based review): report of the Quality Standards Subcommittee of the …

RG Miller, JA Rosenberg, DE Gelinas… - … and Neural Repair, 1999 - journals.sagepub.com
As with other chronic neurologic diseases, many of the problems engendered by the
disease can be managed effectively with a beneficial impact on quality of life and m some …

Riluzole for amyotrophic lateral sclerosis (ALS)/motor neuron disease (MND)

M Rg, M Jd, M DH - Amyotrophic lateral sclerosis and other motor …, 2003 - Taylor & Francis
BACKGROUND: Riluzole 100 mg probably prolongs survival in patients with amyotrophic
lateral sclerosis by about two months and the safety of the drug is not a major concern. The …

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 …

[图书][B] Management of patients with neuromuscular disease

JR Bach - 2003 - researchwithrutgers.com
A great majority of people with neuromuscular diseases like muscular dystrophy, ALS, spinal
muscular atrophy, myasthenia gravis and post-poliomyelitis continue to be told that they …

Management of motor neurone disease

RS Howard, RW Orrell - Postgraduate medical journal, 2002 - academic.oup.com
Motor neurone disease is a progressive neurodegenerative disorder leading to severe
disability and death. It is clinically characterised by mixed upper and lower motor neurone …

[PDF][PDF] Practice parameter: the care of the patient with amyotrophic lateral sclerosis (an evidence-based review)

RG Miller, JA Rosenberg, DF Gelinas, H Mitsumoto… - Neurology, 1999 - Citeseer
Mission statement. The Quality Standards Subcommittee (QSS) of the American Academy of
Neurology (AAN) is charged with developing practice parameters for physicians. This …

Lamotrigine adjunctive therapy in painful phenomena in MS: preliminary observations

C Cianchetti, A Zuddas, AP Randazzo, L Perra… - Neurology, 1999 - AAN Enterprises
Results. The improvement level for paroxysmal limb pain or burning paresthesias was+++ in
2 patients,++ in 5,+ in 1, and 0 in 1; in 8 patients improvement persisted after 1 year …

Cost effectiveness of riluzole in amyotrophic lateral sclerosis

A Messori, S Trippoli, P Becagli, G Zaccara - Pharmacoeconomics, 1999 - Springer
Objective: In patients with amyotrophic lateral sclerosis, long term treatment with riluzole has
been reported to improve survival or tracheostomy-free survival in comparison with placebo …

Current pharmacological management of amyotropic lateral sclerosis and a role for rational polypharmacy

MD Weiss, P Weydt, GT Carter - Expert Opinion on …, 2004 - Taylor & Francis
Amyotropic lateral sclerosis (ALS) is a progressive degenerative condition of motor neurons
that is ultimately fatal. Even though scientific discovery over the past few decades has led to …