To read this article in full you will need to make a payment
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribers receive full online access to your subscription and archive of back issues up to and including 2002.
Content published before 2002 is available via pay-per-view purchase only.
Subscribe:
Subscribe to Critical Care ClinicsAlready a print subscriber? Claim online access
Already an online subscriber? Sign in
Register: Create an account
Institutional Access: Sign in to ScienceDirect
References
- Urea cycle disorders: diagnosis, pathophysiology, and therapy.Adv Pediatr. 1996; 43: 127-170
- Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathy.J Child Neurol. 1995; 10: 369-374
- Natural history of symptomatic partial ornithine transcarbamylase deficiency.N Engl J Med. 1986; 314: 541-547
- Ornithine transcarbamylase deficiency: a case report.Neuropediatrics. 1998; 29: 331-332
- Ornithine transcarbamylase deficiency presenting with strokelike episodes.J Pediatr. 1993; 122: 423-425
- Metabolic disorders mimicking Reye's syndrome.J Formos Med Assoc. 2000; 99: 295-299
- Urea cycle defect: a case with MR and CT findings resembling infarct.Pediatr Radiol. 1991; 21: 594-595
- Atypical clinical course of ornithine transcarbamylase deficiency due to new mutant (comparison with Reye's disease).J Clin Endocrinol Metab. 1979; 48: 388-392
- Cryptogenic hepatitis masking the diagnosis of ornithine transcarbamylase deficiency.J Pediatr Gastroenterol Nutr. 1996; 22: 380-383
- Urea cycle enzymes.in: Scriver C. Beaudet A. Valle D. The metabolic & molecular bases of inherited disease. 8th edition. McGraw-Hill, New York2000: 1909-1963
- Sodium valproate and ornithine carbamyl transferase deficiency.Lancet. 1981; 1: 1165-1166
- Hyperammonaemic encephalopathy after initiation of valproate therapy in unrecognised ornithine transcarbamylase deficiency.J Neurol Neurosurg Psychiatry. 1998; 64: 680-682
- Under recognition of late onset ornithine transcarbamylase deficiency.Arch Dis Child. 2000; 82: 390-391
- CT and MRI in a girl with late-onset ornithine transcarbamylase deficiency: case report.Neuroradiology. 1996; 38: 796-799
- Ornithine carbamoyltransferase deficiency presenting with chorea in a female.J Inherit Metab Dis. 2000; 23: 843-844
- Magnetic resonance spectroscopy shows increased brain glutamine in ornithine carbamoyl transferase deficiency.Pediatr Res. 1993; 33: 77-81
- Acute hemiparesis as the presenting sign in heterozygote for ornithine Ttranscarbamylase deficiency.Neuropediatrics. 1990; 21: 133-135
- Unusual biochemical and clinical features in a girl with ornithine transcarbamylase deficiency.Pediatr Neurol. 1986; 2: 51-53
- Diagnostic value of orotic acid in heritable disorders of the urea cycle and in hyperammonemia due to organic acidurias.Eur J Pediatr. 1980; 134: 109-113
- Alternative pathway therapy for urea cycle disorders: twenty years later.J Pediatr. 2001; 138: S46-S55
- Hyperargininemia due to liver arginase deficiency.Mol Genet Metab. 2005; 84: 243-251
Article info
Footnotes
Dr. Summar acknowledges the support of NIH grants MOI-RR-0095 and U54-RR-019453.
Complete financial disclosure information for each author is provided in the frontmatter of this supplement on page iii.
Identification
Copyright
© 2005 Elsevier Inc. Published by Elsevier Inc. All rights reserved.
