Difficulties in assessing the effect of strychnine on the outcome of non-ketotic hyperglycinaemia. Observations on sisters with a mild T-protein defect
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/BF00439398.pdf
Reference26 articles.
1. Ando T, Nyhan WL, Bicknell J, Harris R, Stern J (1978) Nonketotic hyperglycinaemia in a family with an unusual phenotype. J Inherited Metab Dis 1:79?83
2. Applegarth DA, Edelsten AD, Wong LTK, Morrison BJ (1979) Observed range of assay values for plasma and cerebrospinal fluid amino acid levels in infants and children aged 3 months to 10 years. Clin Biochem 12:173?178
3. Arneson D, Chien LT, Chance P, Wilroy RS (1979) Strychnine therapy in non-ketotic hyperglycinemia. Pediatrics 63:369?373
4. Bank WJ, Morrow G (1972) A familial spinal cord disorder with hyperglycinaemia. Arch Neurol 27:136?144
5. Carson NAJ (1982) Non-ketotic hyperglycinaemia ? a review of 70 patients. J Inherited Metab Dis 5 [Suppl 2]:126?128
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