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Brain amino acid contents are dissimilar in sporadic and Guamanian amyotrophic lateral sclerosis.

Identifieur interne : 001B60 ( PubMed/Curation ); précédent : 001B59; suivant : 001B61

Brain amino acid contents are dissimilar in sporadic and Guamanian amyotrophic lateral sclerosis.

Auteurs : T L Perry [Canada] ; C. Bergeron ; J C Steele ; D R Mclachlan ; S. Hansen

Source :

RBID : pubmed:2250169

English descriptors

Abstract

Amino acid contents were measured in autopsied brains of five Guamanian patients with amyotrophic lateral sclerosis (ALS) or parkinsonism-dementia. Absence of the glutamate deficiency and taurine excess characteristic of sporadic ALS suggest that, despite clinical similarities, Guamanian ALS is a different disorder from sporadic ALS.

PubMed: 2250169

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pubmed:2250169

Le document en format XML

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<name sortKey="Perry, T L" sort="Perry, T L" uniqKey="Perry T" first="T L" last="Perry">T L Perry</name>
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<nlm:affiliation>Department of Pharmacology and Therapeutics, University of British Columbia, Vancouver, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
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<name sortKey="Bergeron, C" sort="Bergeron, C" uniqKey="Bergeron C" first="C" last="Bergeron">C. Bergeron</name>
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<name sortKey="Steele, J C" sort="Steele, J C" uniqKey="Steele J" first="J C" last="Steele">J C Steele</name>
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<name sortKey="Mclachlan, D R" sort="Mclachlan, D R" uniqKey="Mclachlan D" first="D R" last="Mclachlan">D R Mclachlan</name>
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<div type="abstract" xml:lang="en">Amino acid contents were measured in autopsied brains of five Guamanian patients with amyotrophic lateral sclerosis (ALS) or parkinsonism-dementia. Absence of the glutamate deficiency and taurine excess characteristic of sporadic ALS suggest that, despite clinical similarities, Guamanian ALS is a different disorder from sporadic ALS.</div>
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   |texte=   Brain amino acid contents are dissimilar in sporadic and Guamanian amyotrophic lateral sclerosis.
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