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A newborn Screening Programme for Inborn errors of metabolism in Galicia: 22 years of evaluation and follow-up.

Maria-Luz CouceMaría-Dolores BóvedaDaisy E CastiñeirasMaría-Eugenia Vázquez-MosqueraSofía Barbosa-GouveiaMaría-José De CastroAgustin J Iglesias-RodríguezCristóbal ColónJosé A CochoPaula Sánchez
Published in: Orphanet journal of rare diseases (2024)
This study highlights the benefits of collecting urine samples, reduce NBS reporting time and expanding the number of IEMs included in NBS programmes.
Keyphrases
  • adverse drug
  • study protocol
  • patient safety
  • emergency department