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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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A strategy for glycine encephalopathy therapy.

An inherited defect in the glycine cleavage enzyme results in the condition of neonatal glycine encephalopathy which has not responded to the current innovative methods of therapy. A re-examination of the enzyme structure and metabolic pathways, leads us to recommend future clinical evaluation of (1) vitamin-responsiveness, e.g., pyridoxine, folate and lipoic acid, (2) methionine, (3) N5, N10-methylene tetrahydrofolate and (4) alpha-methylserine therapy during the critical period of neonatal brain growth and development.[1]

References

  1. A strategy for glycine encephalopathy therapy. Mendelson, I.S. Journal of mental deficiency research. (1982) [Pubmed]
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