References
Batshaw, M. L., Brusilow, S., Waber, L., Blom, W., Brubakk, A. M., Burton, B. K., Cann, H. M., Kerr, D., Manunes, P., Matalon, R., Myerberg, D. and Schafer, I. A. Treatment of inborn errors of urea synthesis: Activation of alternate pathways of waste urea nitrogen and excretion.N. Engl. J. Med. 306 (1982) 1387–1392
Matsuo, M., Aida, M., Yamada, T. and Takemine, H. Two-year experience of screening for hyperammonemia and a case of neonatal citrullinemia. In Naruse, H. and Irie, M. (eds)Neonatal Screening, Excerpta Medica, Amsterdam, 1983, pp. 388–389
Saheki, T., Takano, K., Kobayashi, K., Imamura, Y., Itakura, Y., Sase, M., Hagihara, S. and Muto, S. Analysis of the enzyme abnormality in eight cases of neonatal and infantile citrullinemia in Japan.J. Inher. Metab. Dis. 8 (1985) 155–156
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Matsoo, M., Takemine, H., Aida, M. et al. Serum arginine level in neonatal citrullinaemia. J Inherit Metab Dis 11, 309–310 (1988). https://doi.org/10.1007/BF01800379
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DOI: https://doi.org/10.1007/BF01800379