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Psychometric analysis of the pediatric quality of life inventory 3.0 neuromuscular module administered to patients with duchenne muscular dystrophy: A rasch analysis.

Erik LandfeldtAnna MayhewVolker StraubHanns LochmüllerKatharine BushbyPeter Lindgren
Published in: Muscle & nerve (2018)
The English version of the PedsQL NMM may not be a valid measure of health-related quality of life in patients with DMD. Muscle Nerve 58: 367-373, 2018.
Keyphrases
  • duchenne muscular dystrophy
  • psychometric properties
  • muscular dystrophy
  • skeletal muscle
  • young adults
  • peripheral nerve