Assessment of a Portable Digital Device for Quantified Analysis of Markerless Walking in Volunteers With Neuromuscular Diseases or Asymptomatic Volunteers
Conditions
Spinal Muscular Atrophy (SMA) · Charcot-Marie-Tooth · Muscular Dystrophy · Myotonic Dystrophy
Simple summaryAI-assisted
This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.
Locations
Centre d'Exploration et d'Évaluation Neuromusculaire, Paris, France
Contact: Study coordinator (Romain FEIGEAN, PhD) · r.feigean@institut-myologie.org · +33 01 42 16 58 80