| Literature DB >> 20698807 |
Ettore Beghi1, Adriano Chiò, Philippe Couratier, Jesùs Esteban, Orla Hardiman, Giancarlo Logroscino, Andrea Millul, Douglas Mitchell, Pierre-Marie Preux, Elisabetta Pupillo, Zorica Stevic, Robert Swingler, Bryan J Traynor, Leonard H Van den Berg, Jan H Veldink, Stefano Zoccolella.
Abstract
Abstract Effective treatments for amyotrophic lateral sclerosis (ALS) have remained elusive. Only riluzole, a drug thought to affect glutamate metabolism, improves survival albeit to modest extent. Explanations for the negative results of therapeutic trials include a likely heterogeneity, both in disease susceptibility and pathogenic mechanisms, and faulty methodology of clinical trials. Further understanding of these factors will lead to improvements in patient stratification, and in the design of future clinical trials.Entities:
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Year: 2010 PMID: 20698807 PMCID: PMC3513399 DOI: 10.3109/17482968.2010.502940
Source DB: PubMed Journal: Amyotroph Lateral Scler ISSN: 1471-180X