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Ketamine and strychnine treatment of an infant with nonketotic hyperglycinaemia

H. Tegtmeyer-Metzdorf, B. Roth, M. Günther, M. Theisohn and U. Heinemann, et al.

European Journal of Pediatrics, 1995, Volume 154, Number 8, Pages 649-653

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Journal Article

Non-ketotic hyperglycinaemia: clinical and biochemical aspects

K. Tada and K. Hayasaka

European Journal of Pediatrics, 1987, Volume 146, Number 3, Pages 221-227

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Journal Article

Treatment of non-ketotic hyperglycinaemia with diazepam, choline and folic acid

R. Matalon, K. Michals, S. Naidu and J. Hughes

Journal of Inherited Metabolic Disease, 1982, Volume 5, Supplement 1, Pages 3-5

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Journal Article

Amino acid loading tests in a patient with non-ketotic hyperglycinaemia

T. Palmer and V. G. Oberholzer

Journal of Inherited Metabolic Disease, 1985, Volume 8, Supplement 2, Pages 125-126

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Journal Article

Modification of fibroblast propionyl CoA carboxylase activity by valine as a possible diagnostic technique in non-ketotic hyperglycinaemia

J. S. Fox

Journal of Inherited Metabolic Disease, 1982, Volume 5, Supplement 2, Pages 121-123

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Journal Article

Threonine dehydratase deficiency: A probable cause of non-ketotic hyperglycinaemia

I. Krieger and F. Booth

Journal of Inherited Metabolic Disease, 1984, Volume 7, Number 2, Pages 53-56

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Journal Article

Non-ketotic hyperglycinaemia presenting as pachygyria

J. M. Fletcher, A. M. E. Bye, V. Nayanar and B. Wilcken

Journal of Inherited Metabolic Disease, 1995, Volume 18, Number 6, Pages 665-668

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Journal Article

A treatment of non-ketotic hyperglycinaemia

S. Schoos-Barbette, J. Gerard, N. Francotte and C. Lambotte

Journal of Inherited Metabolic Disease, 1984, Volume 7, Number 4, Pages 165-167

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