Pompe disease (glycogen storage disease type II): clinical features and enzyme replacement therapy

Research output: Contribution to journalArticleAcademicpeer-review

39 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)82-86
Number of pages5
JournalActa Neurologica Belgica
Volume106
Publication statusPublished - 2006

Research programs

  • EMC MGC-02-96-01
  • EMC MM-01-54-01
  • EMC MM-04-44-02

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