Inborn error of metabolism patients after liver transplantation: Outcomes of 35 patients over 27 years in one pediatric quaternary hospital-Reference-Cited by-同舟云学术

Inborn error of metabolism patients after liver transplantation: Outcomes of 35 patients over 27 years in one pediatric quaternary hospital

Published:2022-01-23 Issue:5 Volume:188 Page:1443-1447
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:American J of Med Genetics Pt A

Author:

Pritchard Amanda Barone¹^ORCID,Izumi Kosuke²^ORCID,Payan‐Walters Irma²,Yudkoff Marc²,Rand Elizabeth B.³,Bhoj Elizabeth²⁴^ORCID

Affiliation:

1. Division of Pediatric Genetics, Metabolism, and Genomic Medicine, Department of Pediatrics C.S. Mott Children's Hospital, Michigan Medicine Ann Arbor Michigan USA

2. Division of Human Genetics, Department of Pediatrics The Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

3. Division of Gastroenterology, Hepatology and Nutrition, Department of Pediatrics The Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

4. Center for Applied Genomics The Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62659

Reference16 articles.

1. Tyrosinemia and Liver Transplantation: Experience at CHU Sainte-Justine

2. Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia

3. The role of orthotopic liver transplantation in the treatment of ornithine transcarbamylase deficiency

4. Metabolic stroke in methylmalonic acidemia five years after liver transplantation

5. Early and Late Complications After Liver Transplantation for Propionic Acidemia in Children: A Two Centers Study

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