Author:
Nyhan W. L.,Rubio V.,Jordá A.,Grisolia S.,Gutierez F.,Canosa C.
Reference18 articles.
1. R.A. Ballard, B. Vinocur, J.W. Reynolds, R.P. Wennberg, A. Merritt, L. Sweetman, and W.L. Nyhan, Transient hyperammonemia of the preterm infant, New Eng. J. Med. 299: 920 (1978).
2. C. Bachmann, G. Schubigger, K.H. Jaggi, S. Krähenbuhl, J.P. Colombo, and 0. Tonz, N-acetylglutamate synthetase deficiency a new disorder of ammonia detoxification, New Eng. J. Med. 304: 543 (1981).
3. S.W. Brusilow, J. Tinker, and M.L. Batshaw, Amino acid acylation: A mechanism of nitrogen excretion in inborn errors of urea synthesis. Science 207: 659 (1980).
4. M.L. Batshaw, and S.W. Brusilow, Treatment of hyperammonemic coma caused by inborn errors of urea synthesis. J. Pediat. 97: 893 (1980).
5. S. Brusilow, and M.L. Batshaw, Arginine therapy of argininosuccinase deficiency, Lancet 1: 125 (1979).
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A new case of arginase deficiency in a Spanish male;Journal of Inherited Metabolic Disease;1986-12
2. Liver pathology in transient neonatal hyperammonemia;Virchows Archiv A Pathological Anatomy and Histopathology;1983