Successful treatment of severe OTC deficiency.
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[1] S. Brusilow,et al. New approaches to the diagnosis and treatment of inborn errors or urea synthesis. , 1981, Pediatrics.
[2] M. Yudkoff,et al. Ornithine transcarbamylase deficiency in a boy with normal development , 1980 .
[3] S. Brusilow,et al. Amino acid acylation: a mechanism of nitrogen excretion in inborn errors of urea synthesis. , 1980, Science.
[4] S. Brusilow,et al. NEW PATHWAYS OF NITROGEN EXCRETION IN INBORN ERRORS OF UREA SYNTHESIS , 1979, The Lancet.
[5] P. J. Snodgrass,et al. Atypical clinical course of ornithine transcarbamylase deficiency due to a new mutant (comparison with Reye's disease). , 1979, The Journal of clinical endocrinology and metabolism.
[6] S. Brusilow,et al. Treatment of complete ornithine transcarbamylase deficiency with nitrogen-free analogues of essential amino acids. , 1978, The Journal of pediatrics.
[7] C. Scriver,et al. Partial ornithine carbamyl transferase deficiency: an inborn error of the urea cycle presenting as orotic aciduria in a male infant. , 1972, Canadian Medical Association journal.
[8] Howard B. Lewis,et al. The synthesis and rate of elimination of hippuric acid after benzoate ingestion in man , 1914 .
[9] S. Brusilow,et al. Therapy of urea cycle enzymopathies: three case studies. , 1981, The Johns Hopkins medical journal.
[10] Ruth Griffiths,et al. The Abilities of Babies: A Study in Mental Measurement , 1954 .