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Phenylketonuria (PKU) Urinary Metabolomic Phenotype Is Defined by Genotype and Metabolite Imbalance: Results in 51 Early Treated Patients Using Ex Vivo 1H-NMR Analysis.
Cannet, Claire; Bayat, Allan; Frauendienst-Egger, Georg; Freisinger, Peter; Spraul, Manfred; Himmelreich, Nastassja; Kockaya, Musa; Ahring, Kirsten; Godejohann, Markus; MacDonald, Anita; Trefz, Friedrich.
Afiliação
  • Cannet C; Bruker Biospin, 76275 Ettlingen, Germany.
  • Bayat A; Kennedy Centre, Center for PKU, 2600 Glostrup, Denmark.
  • Frauendienst-Egger G; Department of Pediatrics, School of Medicine, University of Tübingen, 72074 Tübingen, Germany.
  • Freisinger P; Department of Pediatrics, School of Medicine, University of Tübingen, 72074 Tübingen, Germany.
  • Spraul M; Bruker Biospin, 76275 Ettlingen, Germany.
  • Himmelreich N; CEGAT, Human Genetic Institute, 72076 Tübingen, Germany.
  • Kockaya M; Private Pediatric Practice, 68307 Mannheim, Germany.
  • Ahring K; Kennedy Centre, Center for PKU, 2600 Glostrup, Denmark.
  • Godejohann M; Bruker Biospin, 76275 Ettlingen, Germany.
  • MacDonald A; Dietetic Department, Birmingham Children's Hospital, Birmingham B4 6NH, UK.
  • Trefz F; Metabolic Consulting Reutlingen, 72766 Reutlingen, Germany.
Molecules ; 28(13)2023 Jun 22.
Article em En | MEDLINE | ID: mdl-37446577
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenilcetonúrias Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenilcetonúrias Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article