A clinicopathological study of patient with familial amyotrophic lateral sclerosis associated with a two-base pair deletion in the copper/zinc superoxide dismutase (SOD1) gene

Acta Neuropathol. 2001 Apr;101(4):415.

Authors

J Kadekawa¹, H Fujimura, T Yanagihara, S Sakoda

Affiliation

¹ Department of Neurology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita Osaka 565-0871, Japan.

PMID: 11355314

No abstract available

MeSH terms

Anterior Horn Cells / enzymology
Anterior Horn Cells / ultrastructure
Antibodies, Monoclonal / immunology
Artifacts
Brain Ischemia / etiology
Brain Ischemia / metabolism
Coma / etiology
Coma / metabolism
False Negative Reactions
Humans
Lewy Bodies / enzymology
Lewy Bodies / ultrastructure
Motor Neuron Disease / complications
Motor Neuron Disease / enzymology*
Motor Neuron Disease / genetics
Nerve Tissue Proteins / chemistry
Nerve Tissue Proteins / genetics*
Sequence Deletion*
Superoxide Dismutase / chemistry
Superoxide Dismutase / genetics*

Substances

Antibodies, Monoclonal
Nerve Tissue Proteins
Superoxide Dismutase