Secondary carnitine deficiency in hyperammonemic attacks of ornithine transcarbamylase deficiency
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference30 articles.
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2. Neurologic outcome in children with inborn errors of urea synthesis: outcome of urea-cycle enzymopathies;Msall;N Engl J Med,1984
3. Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency;Batshaw;J Pediatr,1986
4. Reye's syndrome due to a novel protein-tolerant variant of ornithine-transcarbamylase deficiency;Thaler;Lancet,1974
5. Partial ornithine transcarbamylase deficiency simulating Reye syndrome;Yokoi;J Pediatr,1981
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