Skip to Main Content

Paper Details

Domino liver transplant from a donor with maple syrup urine disease into a recipient with phenylketonuria.
Molecular Genetics and Metabolism Reports
2
2022
Classical phenylketonuria, PKU, branched chain ketoacid, branched chain ketoacid dehydrogenase, branched chain ketoacid dehydrogenase deficiency, hyperphenylalaninemia, maple syrup urine disease, maternal PKU Syndrome, patient, patients, phenylalanine, phenylketonuria, woman, women
Author NameAffiliation
Steven F DobrowolskiUPMC Children's Hospital
Rakesh SindhiHillman Center for Pediatric Transplantation, UPMC Children's Hospital of Pittsburgh
Kevin A StraussClinic for Special Children
Kevin A StraussPenn Medicine-Lancaster General Hospital
Kevin A StraussUniversity of Massachusetts School of Medicine
George V MazariegosHillman Center for Pediatric Transplantation, UPMC Children's Hospital of Pittsburgh
Jerry VockleyUniversity of Pittsburgh School of Medicine, UPMC Children's Hospital of Pittsburgh
Kyle SoltysHillman Center for Pediatric Transplantation, UPMC Children's Hospital of Pittsburgh
  • 1 - 8

Datasets

Release 1.2