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.

Author:

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference44 articles.

1. Forty four patients were included in clinically diagnosed patients27 28 and therefore that population based study between 1925-84 may be a useful method for following trends in giving a crude incidence of 2-0/100 000/year this disease

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3. Familial adult motor neuron disease: amyotrophic lateral sclerosis;Mulder, D.W.; Kurland, L.T.; Offord, K.P.; Beard, C.M.;Neurology,1986

4. Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity;SiddiqueT, Figlewicz D.A.; MA, Pericak-Vance;N EnglJ Med,1991

5. Amyotrophic lateral sclerosis: Part 2. Etiopathogenesis;Tandan, R.; Bradley, W.G.;Ann Neurol,1985

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