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People diagnosed with ALS live on average 2–4 years after diagnosis due to the quick progression of the disease. [2] [3] The progression and severity of ALS is rated by doctors on the ALS Functional Rating Scale, which has been revised and is referred to as ALSFRS-R.
The rate of progression can be measured using the ALS Functional Rating Scale - Revised (ALSFRS-R), a 12-item instrument survey administered as a clinical interview or self-reported questionnaire that produces a score between 48 (normal function) and 0 (severe disability). [37]
Articles relating to amyotrophic lateral sclerosis (ALS), also known as motor neurone disease (MND) or Lou Gehrig's disease. It is a specific disease which causes the death of neurons controlling voluntary muscles. ALS is characterized by stiff muscles, muscle twitching, and gradually worsening weakness due to muscles decreasing in size.
Denali said their drug did not meet the main goal of change in the ALS functional rating scale, which measures deviations from "normal" motor functioning as caused by ALS. ... ALS is a rare ...
The following diagnostic systems and rating scales are used in psychiatry and clinical psychology. This list is by no means exhaustive or complete. This list is by no means exhaustive or complete. For instance, in the category of depression, there are over two dozen depression rating scales that have been developed in the past eighty years.
This page was last edited on 24 October 2024, at 14:38 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
Functional Rating Scale for Emotional and Social Functioning Capacities: to evaluate the child's communication skills and expressions of thoughts and feelings. The Parent-Infant Relationship Global Assessment Scale (PIR-GAS; from Axis II ) : to evaluate the quality of a caregiver-child relationship and identify relationship disorders.
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