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The Capital Region of Denmark - a part of Copenhagen University Hospital
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When should social service referral be considered in phenylketonuria?

Research output: Contribution to journalJournal articleResearchpeer-review

  1. The impact of consanguinity on the frequency of inborn errors of metabolism

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Residual OCTN2 transporter activity, carnitine levels and symptoms correlate in patients with primary carnitine deficiency.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Neonatal mitochondrial hepatoencephalopathy caused by novel GFM1 mutations

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Overweight and obesity in PKU: The results from 8 centres in Europe and Turkey

    Research output: Contribution to journalJournal articleCommunication

  1. The complete European guidelines on phenylketonuria: diagnosis and treatment

    Research output: Contribution to journalReviewResearchpeer-review

  2. Key European guidelines for the diagnosis and management of patients with phenylketonuria

    Research output: Contribution to journalJournal articleResearchpeer-review

  • Margreet van Rijn
  • Kirsten Ahring
  • Amaya Bélanger-Quintana
  • Kathi Dokoupil
  • Hulya Gokmen-Ozel
  • Anna Maria Lammardo
  • Martine Robert
  • Júlio César Rocha
  • Anita MacDonald
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Original languageEnglish
JournalMolecular Genetics and Metabolism Reports
Volume2
Pages (from-to)85-88
DOIs
Publication statusPublished - Mar 2015

ID: 46011880