Survival prediction in amyotrophic lateral sclerosis
- 1 October 1989
- journal article
- research article
- Published by Wiley in Muscle & Nerve
- Vol. 12 (10) , 833-841
- https://doi.org/10.1002/mus.880121008
Abstract
This longitudinal study of 194 patients with sporadic ALS demonstrated that it is possible for physicians to predict the approximate survival time for an individual ALS patient given: (1) the age of the patient, (2) the duration of his weakness and (3) an estimate of his clinical disability (ALS Score). This information is of value in the clinical management of ALS patients, and it should facilitate construction of experimental therapeutic trials in ALS.This publication has 13 references indexed in Scilit:
- Presalvage prostate‐specific antigen (PSA) and PSA doubling time as predictors of biochemical failure of salvage cryotherapy in patients with locally recurrent prostate cancer after radiotherapyCancer, 2006
- A rating scale for amyotrophic lateral sclerosis: Description and preliminary experienceAnnals of Neurology, 1987
- Quantitative motor assessment in amyotrophic lateral sclerosisNeurology, 1986
- Transfer factor is ineffective in amyotrophic lateral sclerosisAnnals of Neurology, 1979
- Spirometry in Amyotrophic Lateral SclerosisArchives of Neurology, 1979
- Double‐blind study of modified neurotoxin in motor neuron diseaseNeurology, 1979
- Amyotrophic Lateral SclerosisArchives of Neurology, 1978
- MOTOR NEURON DISEASEActa Neurologica Scandinavica, 1977
- Design and analysis of randomized clinical trials requiring prolonged observation of each patient. II. Analysis and examplesBritish Journal of Cancer, 1977
- The administration of guanidine in amyotrophic lateral sclerosisNeurology, 1974