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The ALSFRS-R is a simple, validated, and reliable tool for evaluating decline in function. Scores decline with disease progression at a rate that is generally consistent across clinical trials.1,2. See the full ALSFRS-R questionnaire on reverse. * There are different assessments for cutting food with gastrostomy.
Overview: The Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS) is an instrument for evaluating the functional status of patients with Amyotrophic Lateral Sclerosis. It can be used to monitor functional change in a patient over time. Interpretation: minimum score: 0 maximum score: 40 The higher the score the more function is retained.
This document is a list of passers of the ALS Accreditation and Equivalency Test for the secondary level held in October 2009. It includes the last name, first name, middle name, and testing center of 1,119 individuals who passed the exam. The passers are listed in alphabetical order by last name.
ALS is characterized by degeneration of the cor-tical motor neurons and their axons (upper motor neuron) and of the motor neurons in the cranial nerve nuclei and in the spinal cord (lower motor neuron) with the exception of the oculomotor and the sphincter muscles.
Die amyotrophe Lateralsklerose ist eine progressive Krankheit mit verschiedenen Symptomen. Um alle Symptome in einem Assessment zu erfassen, muss dies breit gefächert sein. Das trifft zum Beispiel auf die ALS Functional Rating Scale zu.
The ALSSQOL-R has successfully been implemented in a multidisciplinary ALS clinic. The Penn State Hershey ALS Clinic has paired the ALSSQOL-R with a self-reported ALS Functional Rating Scale-Revised (ALSFRS-R) 1 as a pre-clinic assessment. Patients complete the assessment in a paper or computer format prior to their scheduled appointment.
3 Ιαν 2014 · Measures activities of daily living (ADL) and global function for patients with Amyotrophic Lateral Sclerosis (ALS)
