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Abnormal glycine metabolism in motor neurone disease: studies on plasma and cerebrospinal fluid.

Plasma amino acid levels were measured following oral glycine loading in 43 patients with motor neurone disease (MND), eight normal subjects and 18 neurological disease controls with wasting or spasticity from a variety of other causes. Levels at baseline and 1.5 h after loading did not differ, but...

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Bibliographic Details
Main Authors: Lane, R J, Bandopadhyay, R, de Belleroche, J
Format: Artigo
Language:Inglês
Published: 1993
Subjects:
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1294093/
https://ncbi.nlm.nih.gov/pubmed/8410884
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