Acute hyperammonemic encephalopathy in adult onset ornithine transcarbamylase deficiency
Author:
Publisher
Springer Science and Business Media LLC
Subject
Critical Care and Intensive Care Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00134-008-1217-2.pdf
Reference10 articles.
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2. Chang MY, Fang JT, Chen YC, Huang CC (1999) Continuous venovenous haemofiltration in hyperammonemic coma of an adult with non-diagnosed partial ornithine transcarbamylase deficiency. Nephrol Dial Transplant 14:1282–1284
3. King LS, Singh RH, Rhead WJ, Smith W, Lee B, Summar ML (2005) Genetic counselling issues in urea cycle disorders. Crit Care Clin 21:S37–S44
4. Tuchman M, Plante RJ, McCann MT, Qureshi AA (1994) Seven new mutations in the human ornithine transcarbamylase gene. Hum Mutat 4:57–60
5. Summar ML, Barr F, Dawling S, Smith W, Lee B, Singh RH, Rhead WJ, King LS, Christman BW (2005) Unmasked adult-onset urea cycle disorders in the critical care setting. Crit Care Clin 21:S1–S8
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