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Table of contents
1. INTRODUCTION
1.1. Amyotrophic lateral sclerosis: clinical features, diagnosis and care…
1.1.1. Riluzole
1.1.2. Multidisciplinary care
1.1.3. Nutrition
1.1.4. Respiration
1.1.5. Palliative care
1.1.6. Symptomatic therapy
1.2. Epidemiology
1.2.1. Incidence and mortality
1.2.2 Risk factors
1.3. Measuring progression
1.4. Clinical features that predict survival
1.5. Clinical trials
1.6. Major questions
2. CHANGING MORTALITY FOR MOTOR NEURON DISEASE IN FRANCE (1968-2007): AN AGE-PERIOD-COHORT ANALYSIS
2.1. Results
3. IMPROVING SURVIVAL IN A LARGE ALS CENTER COHORT…
3.1. Results
4. PREDICTING SURVIVAL IN ALS AT PRESENTATION: A 15-YEAR EXPERIENCE
4.1. Results
5. SUMMARY
6. CONCLUSIONS AND PERSPECTIVE
7. BIBLIOGRAPHY




