Health outcome and quality-of-life measurements in amyotrophic lateral sclerosis
β Scribed by Michael Swash
- Publisher
- Springer
- Year
- 1997
- Tongue
- English
- Weight
- 404 KB
- Volume
- 244
- Category
- Article
- ISSN
- 0340-5354
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
It is now possible to slow the disease progression of amyotrophic lateral sclerosis (ALS), but documented improvement in the quality of life of ALS patients has been difficult to quantitate. Putative mechanisms involved in motor neuron degeneration in ALS include oxidative damage, mitochondrial dysf
Objective: To examine the care of patients with ALS following the publication of the standardized recommendations for the management of patients with amyotrophic lateral sclerosis (ALS) published in 1999 by the American Academy of Neurology. Methods: Specific aspects of ALS patient management have b