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Living donor liver transplantation from an asymptomatic mother who was a carrier for ornithine transcarbamylase deficiency

  • Published:2012-05-14 Issue:6 Volume:16 Page:E196-E200
  • ISSN:1397-3142
  • Container-title:Pediatric Transplantation
  • language:en
  • Short-container-title:

Author:

Wakiya T.,Sanada Y.,Urahashi T.,Ihara Y.,Yamada N.,Okada N.,Egami S.,Sakamoto K.,Murayama K.,Hakamada K.,Yasuda Y.,Mizuta K.

Publisher

Wiley

Subject

Transplantation,Pediatrics, Perinatology and Child Health

Reference20 articles.

1. The clinical, biochemical, and molecular spectrum of ornithine transcarbamylase deficiency;Tuchman;J Lab Clin Med,1992

2. Prospective treatment of urea cycle disorders;Maestri;J Pediatr,1991

3. Neurodevelopmental outcome of long-term therapy of urea cycle disorders in Japan;Uchino;J Inherit Metab Dis,1998

4. X-inactivation pattern in the liver of a manifesting female with ornithine transcarbamylase (OTC) deficiency;Yorifuji;Clin Genet,1998

5. Orthotopic liver transplantation for ornithine transcarbamylase deficiency with hyperammonemic encephalopathy;Hasegawa;J Pediatr Surg,1995
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