BACKGROUND: Myotonic dystrophy type 1 (DM1) is a rare, inherited chronic progressive disease as well as an autosomal dominant multi-systemic disorder. It is probably one of the most common adult forms of muscular dystrophy, with a prevalence of approximately 10 per 100,000 people affected. With 733 million people in Europe, we estimate that 75,000 people in Europe are affected with DM1. METHODS/DESIGN: OPTIMISTIC is a multi-centre, randomised trial designed to compare an intervention comprising cognitive behavioural therapy (CBT) plus graded exercise therapy against standard care. Participants will be recruited from myotonic dystrophy clinics and neuromuscular centres in France, Germany, the Netherlands and the United Kingdom. A sample size...
BACKGROUND: In individuals with neuromuscular diseases (NMD), symptoms of muscle weakness, fatigue a...
Contains fulltext : 89175.pdf (publisher's version ) (Open Access)BACKGROUND: Stre...
BACKGROUND: In facioscapulohumeral dystrophy (FSHD) muscle function is impaired and declines over ti...
Background: Myotonic dystrophy type 1 (DM1) is a rare, inherited chronic progressive disease as well...
Background: Myotonic dystrophy type 1 (DM1) is a rare, inherited chronic progressive disease as well...
Background: Myotonic dystrophy type 1 is the most common form of muscular dystrophy in adults and le...
International audienceBackground:The European OPTIMISTIC clinical trial has demonstrated a significa...
This study was funded by the European Union Seventh Framework Program, under grant agreement number ...
Background: In individuals with neuromuscular diseases (NMD), symptoms of muscle weakness, fatigue a...
BACKGROUND: In individuals with neuromuscular diseases (NMD), symptoms of muscle weakness, fatigue a...
Objective: The aim of this phase 2 trial was to ascertain the feasibility and effect of community ba...
BACKGROUND: Strength training or aerobic exercise programmes might optimise muscle and cardiorespira...
Myotonic dystrophy type 1 (DM1) is the most frequent muscular dystrophy worldwide with complex, mult...
BACKGROUND: In individuals with neuromuscular diseases (NMD), symptoms of muscle weakness, fatigue a...
Contains fulltext : 89175.pdf (publisher's version ) (Open Access)BACKGROUND: Stre...
BACKGROUND: In facioscapulohumeral dystrophy (FSHD) muscle function is impaired and declines over ti...
Background: Myotonic dystrophy type 1 (DM1) is a rare, inherited chronic progressive disease as well...
Background: Myotonic dystrophy type 1 (DM1) is a rare, inherited chronic progressive disease as well...
Background: Myotonic dystrophy type 1 is the most common form of muscular dystrophy in adults and le...
International audienceBackground:The European OPTIMISTIC clinical trial has demonstrated a significa...
This study was funded by the European Union Seventh Framework Program, under grant agreement number ...
Background: In individuals with neuromuscular diseases (NMD), symptoms of muscle weakness, fatigue a...
BACKGROUND: In individuals with neuromuscular diseases (NMD), symptoms of muscle weakness, fatigue a...
Objective: The aim of this phase 2 trial was to ascertain the feasibility and effect of community ba...
BACKGROUND: Strength training or aerobic exercise programmes might optimise muscle and cardiorespira...
Myotonic dystrophy type 1 (DM1) is the most frequent muscular dystrophy worldwide with complex, mult...
BACKGROUND: In individuals with neuromuscular diseases (NMD), symptoms of muscle weakness, fatigue a...
Contains fulltext : 89175.pdf (publisher's version ) (Open Access)BACKGROUND: Stre...
BACKGROUND: In facioscapulohumeral dystrophy (FSHD) muscle function is impaired and declines over ti...