Clinical phenotypes and natural progression for motor neuron disease: Analysis from an Australian database
Author:
Publisher
Informa UK Limited
Subject
Clinical Neurology,Neurology,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1080/17482960802195871
Reference23 articles.
1. The Scottish Motor Neuron Disease Register: a prospective study of adult onset motor neuron disease in Scotland. Methodology, demography and clinical features of incident cases in 1989.
2. The National Registry of Veterans with Amyotrophic Lateral Sclerosis: Department of Veterans Affairs Cooperative Studies Program (CSP) #500a
3. The ALS Patient Care Database: Goals, design, and early results
4. Survival of Patients with Amyotrophic Lateral Sclerosis in a Population-Based Registry
5. Incidence and prevalence of ALS in Ireland, 1995-1997: A population-based study
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