Public support for neonatal screening for Pompe disease, a broad-phenotype condition

Stephanie Shifra Weinreich*, Tessel Rigter, Carla Geertruida van El, Wybo Jan Dondorp, Pieter Johannes Kostense, Ans T. van der Ploeg, Arnold J. J. Reuser, Martina Cornelia Cornel, Marloes Louise Catharina Hagemans

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

14 Citations (Web of Science)
Original languageEnglish
Pages (from-to)15
JournalOrphanet Journal of Rare Diseases
Publication statusPublished - 14 Mar 2012


  • Neonatal screening
  • Glycogen storage disease type II
  • Technology assessment
  • Biomedical
  • Health policy
  • Consumer participation

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