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An instrumented timed up and go in facioscapulohumeral muscular dystrophy.

Jessie M HuisingaAdam BruetschAyla MccalleyMelissa CurrenceLaura HerbelinOmar JawdatMamatha PasnoorMazen DimachkieRichard BarohnJeffrey M Statland
Published in: Muscle & nerve (2017)
The iTUG was reliable, abnormal in FSHD, and could distinguish between participants with differing disease severities. Instrumenting timed functional tasks may prove to be useful in FSHD clinical trials. Muscle Nerve 57: 503-506, 2018.
Keyphrases
  • muscular dystrophy
  • clinical trial
  • duchenne muscular dystrophy
  • working memory
  • skeletal muscle
  • peripheral nerve
  • phase ii
  • phase iii
  • double blind
  • virtual reality