Author:
Morsy Manal A.,Caskey C. Thomas
Reference37 articles.
1. Maestri N., Hauser E., Bartholomew D., Brusilow S.W., 1991, Prospective treatment of urea cycle disorder, J. Pediatr. 119:923–928.
2. Bmsilow, S. W. and Horwich, A. L. In: The metabolic basis of inherited disease, Vol 6 (Scriver CR, Beaudet AL, Sly WS and Valle D, Eds) New York: McGraw-Hill, pp 629–670. (1989)
3. Finkelstein J., Hauser E., Leonard C., Brusilow S., 1990, Late-onset ornithine transcarbamylase deficiency in male patients, J. Pediatr. 117(6):(6)897–902.
4. Batshaw M., Msall M., Beaudate A., Trojak J., 1986, Risk of serious illness in heterozygotes for Ornithin Transcarbamylase deffeciency, J. Pediatr. 108:236–241.
5. Rowe P., Newman S., Brusilow S.W., 1986, Natural history of symptomatic partial ornithine transcarbamylase deficiency, New Engl Med, 314:541–547.
Cited by
6 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