Hyperammonemia in ornithine transcarbamylase-deficient recipients following living donor liver transplantation from heterozygous carrier donors-Reference-Cited by-同舟云学术

Hyperammonemia in ornithine transcarbamylase-deficient recipients following living donor liver transplantation from heterozygous carrier donors

Published:2016-11-28 Issue:1 Volume:21 Page:e12848
ISSN:1397-3142
Container-title:Pediatric Transplantation
language:en
Short-container-title:Pediatr Transplantation

Author:

Rahayatri Tri Hening¹,Uchida Hajime¹,Sasaki Kengo¹,Shigeta Takanobu¹,Hirata Yoshihiro¹,Kanazawa Hiroyuki¹,Mali Vidyadhar¹,Fukuda Akinari¹,Sakamoto Seisuke¹,Kasahara Mureo¹

Affiliation:

1. Organ Transplantation Center; National Center for Child Health and Development; Tokyo Japan

Funder

Ministry of Health, Labour and Welfare

Publisher

Wiley

Subject

Transplantation,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/petr.12848/fullpdf

Reference21 articles.

1. Diagnosis and treatment of urea cycle disorders;Häberle;J Pediatr Sci,2011

2. Neurological implications of urea cycle disorders;Gropman;J Inherit Metab Dis,2007

3. High urgency liver transplantation in ornithine transcarbamylase deficiency presenting with acute liver failure;Teufel;Pediatr Transplant,2011

4. Long-term outcomes in ornithine transcarbamylase deficiency: a series of 90 patients;Brassier;Orphanet J Rare Dis,2015

5. Coagulopathy unmasking hepatic failure in a child with ornithine transcarbamylase deficiency;Samuel;Isr Med Assoc J,2013

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1. Hyperammonemia in a carbamoyl-phosphate synthetase 1 deficiency recipient after living-donor liver transplantation from a carrier donor: a case report;Frontiers in Medicine;2024-01-03

2. Evaluation of living donors for hereditary liver disease (siblings, heterozygotes);Journal of Hepatology;2023-06

3. Anesthesia management protocol for liver transplantation as treatment for ornithine transcarbamylase deficiency;Pediatric Anesthesia;2023-05-04

4. Early allograft dysfunction in a pediatric liver allograft with an occult pathogenic mutation in the urea cycle;American Journal of Transplantation;2023-05

5. Urea cycle disorders and indications for liver transplantation;Frontiers in Pediatrics;2023-03-03