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PMID: 11442322 Published · ppublish English Journal Article Review

Amyotrophic lateral sclerosis: pathogenesis.

Seminars in neurology ·Vol. 21 ·No. 2 ·2001-06-00 ·Pages 131-9

Brown RH, Robberecht W

Abstract

Amyotrophic lateral sclerosis (ALS) is a devastating paralytic disorder caused by motor neuron degeneration. A subgroup of familial cases arises from mutations in the gene encoding cytosolic superoxide dismutase (SOD1). This review considers insight now being gained into ALS pathogenesis from the study of mutant SOD1 protein and its possible mechanisms of adverse effect on nerve cells. Also discussed are the status of other genetic forms of ALS and the elusive question of why this disorder so specifically targets motor neurons. Ultimately, it is hoped that insights from these types of studies will improve the prospects for developing meaningful therapies of ALS.

MeSH Terms
Amyotrophic Lateral Sclerosis/genetics,physiopathology Animals Humans Mice Motor Neurons/physiology Mutation/genetics Neurons/physiology Superoxide Dismutase/genetics Superoxide Dismutase-1
Chemicals
SOD1 protein, human Sod1 protein, mouse Superoxide Dismutase Superoxide Dismutase-1
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Brown R H
Department of Neurology, University of Leuven School of Medicine, University Hospital Gasthuisberg, Belgium.
Robberecht W
Article Info
Journal
Seminars in neurology
Abbr.
Semin Neurol
ISSN
0271-8235
Published
2001-06-00
Pages
131-9
Language
English
Region
United States
NLM ID
8111343
Subset
IM
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