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Early allograft dysfunction in a pediatric liver allograft with an occult pathogenic mutation in the urea cycle.
Rezvani, Milad; Campbell, Kathleen M; Prada, Carlos E; Peters, Anna L.
  • Rezvani M; Department of Pediatrics, Division of Pediatric Gastroenterology, Hepatology, & Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA; Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Pe
  • Campbell KM; Department of Pediatrics, Division of Pediatric Gastroenterology, Hepatology, & Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
  • Prada CE; Division of Genetics, Genomics and Metabolism, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA; Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
  • Peters AL; Department of Pediatrics, Division of Pediatric Gastroenterology, Hepatology, & Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA. Electronic address: Anna.Peters@cchmc.or
Am J Transplant ; 23(5): 673-675, 2023 05.
Article en En | MEDLINE | ID: mdl-36870389
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Aciduria Argininosuccínica Límite: Child / Humans Idioma: En Año: 2023 Tipo del documento: Article
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Aciduria Argininosuccínica Límite: Child / Humans Idioma: En Año: 2023 Tipo del documento: Article