Argininosuccinic aciduria: Long-term treatment with arginine
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01800042
Reference19 articles.
1. Batshaw, M. L., Brusilow, S., Waber, L., Blom, W., Brubakk, A. M., Burton B. K., Cann, H. M., Kerr, D., Mamunes, P., Matalon, R., Myerberg, D. and Schafer, I. A. Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretion.N. Engl. J. Med. 306 (1982) 1387–1392
2. Brusilow, S. W. and Batshaw, M. L. Arginine therapy of argininosuccinase deficiency.Lancet 1 (1979) 24–27
3. Brusilow, S. W., Danney, M., Waber, L. J., Batshaw, M., Burton, B., Levitsky, L., Roth, K., McKeethren, C. and Ward, J. Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis.N. Engl. J. Med. 310 (1984) 1630–1634
4. Brusilow, S. W. Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis.J. Clin. Invest. 74 (1984) 2144–2148
5. Carter, R. J. and Snyder, F. F. Measurement of aspartylglucosamine in physiological fluids with an amino acid analyzer: fused peak analysis with dual photometers.Analyt. Biochem. 116 (1981) 273–279
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