Pages that link to "Q35668084"
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The following pages link to Cognitive behaviour therapy plus aerobic exercise training to increase activity in patients with myotonic dystrophy type 1 (DM1) compared to usual care (OPTIMISTIC): study protocol for randomised controlled trial (Q35668084):
Displaying 21 items.
- The UK Myotonic Dystrophy Patient Registry: facilitating and accelerating clinical research (Q33627845) (← links)
- Disease awareness in myotonic dystrophy type 1: an observational cross-sectional study. (Q36765372) (← links)
- Measuring Habitual Physical Activity in Neuromuscular Disorders: A Systematic Review (Q37693358) (← links)
- Functional impairment in patients with myotonic dystrophy type 1 can be assessed by an ataxia rating scale (SARA). (Q37730987) (← links)
- Routinely collected data for randomized trials: promises, barriers, and implications (Q47547328) (← links)
- Five-year study of quality of life in myotonic dystrophy (Q47651059) (← links)
- Cognitive impairment and quality of life in patients with myotonic dystrophy type 1. (Q47691178) (← links)
- Treating pediatric neuromuscular disorders: The future is now. (Q52756417) (← links)
- Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease (Q57160865) (← links)
- Neuropsychological and Psychological Functioning Aspects in Myotonic Dystrophy Type 1 Patients in Italy (Q57300169) (← links)
- Outcome Measures for Central Nervous System Evaluation in Myotonic Dystrophy Type 1 May Be Confounded by Deficits in Motor Function or Insight (Q58586761) (← links)
- A Review of Psychopathology Features, Personality, and Coping in Myotonic Dystrophy Type 1 (Q58803315) (← links)
- Cognitive behavioural therapy with optional graded exercise therapy in patients with severe fatigue with myotonic dystrophy type 1: a multicentre, single-blind, randomised trial (Q63367566) (← links)
- Structural white matter networks in myotonic dystrophy type 1. (Q64907740) (← links)
- The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care. (Q64943750) (← links)
- Analyzing walking speeds with ankle and wrist worn accelerometers in a cohort with myotonic dystrophy (Q89485441) (← links)
- Lower extremity muscle pathology in myotonic dystrophy type 1 assessed by quantitative MRI (Q92225672) (← links)
- Genetic determinants of disease severity in the myotonic dystrophy type 1 OPTIMISTIC cohort (Q92507911) (← links)
- Analysis of the functional capacity outcome measures for myotonic dystrophy (Q92554673) (← links)
- MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1 (Q95729094) (← links)
- A Practical Approach to Managing Patients With Myasthenia Gravis-Opinions and a Review of the Literature (Q98177554) (← links)