BACKGROUND: Duchenne Muscular Dystrophy (DMD) is a neuromuscular disorder that presents in childhood and is characterized by slowly progressive proximal weakness and lower extremity contractures that limit ambulatory ability [1, 2]. Contractures develop in the ankles, knees, and hips due to muscle imbalances, fibrotic changes, loss of strength, and static positioning [2, 5]. Currently, standards of care guidelines emphasize the importance of maintaining good musculoskeletal alignment through stretching, bracing, and glucocorticoid (GC) therapy to preserve strength and function. METHODS: This is a retrospective analysis of prospectively collected data through the CINRG Duchenne Natural history study (DNHS). The objectives of this analysis ar...
Contains fulltext : 174808.pdf (publisher's version ) (Open Access)BACKGROUND: The...
This study aimed to investigate possible asymmetries and relationships between performance of domina...
Duchenne muscular dystrophy is a rare genetic disorder with life-limiting pathology. Drisapersen ind...
Objectives. In Duchenne muscular dystrophy, quadriceps weakness is recognized as a key factor in ga...
BACKGROUND: Duchenne muscular dystrophy (DMD) is a rare x-linked recessive genetic disorder affectin...
The timed 4-stair climb (4SC) assessment has been used to measure function in Duchenne muscular dyst...
Neuromuscular disorders are characterised by progressive muscle weakness, which in time causes funct...
International audienceObjective: The main aim was to explore the changes in hand-grip strength in pa...
peer reviewedThe field of translational research in Duchenne muscular dystrophy (DMD) has been trans...
Item does not contain fulltextThe field of translational research in Duchenne muscular dystrophy (DM...
OBJECTIVE: The main aim was to explore the changes in hand-grip strength in patients with Duchenne m...
INTRODUCTION: Duchenne muscular dystrophy (DMD) subjects ≥5 years with nonsense mutations were follo...
The development of new therapeutic agents for the treatment of Duchenne muscular dystrophy has put a...
The timed 4-stair climb (4SC) assessment has been used to measure function in Duchenne muscular dyst...
Duchenne muscular dystrophy (DMD) is a progressive X-linked genetic neuromuscular disorder that prim...
Contains fulltext : 174808.pdf (publisher's version ) (Open Access)BACKGROUND: The...
This study aimed to investigate possible asymmetries and relationships between performance of domina...
Duchenne muscular dystrophy is a rare genetic disorder with life-limiting pathology. Drisapersen ind...
Objectives. In Duchenne muscular dystrophy, quadriceps weakness is recognized as a key factor in ga...
BACKGROUND: Duchenne muscular dystrophy (DMD) is a rare x-linked recessive genetic disorder affectin...
The timed 4-stair climb (4SC) assessment has been used to measure function in Duchenne muscular dyst...
Neuromuscular disorders are characterised by progressive muscle weakness, which in time causes funct...
International audienceObjective: The main aim was to explore the changes in hand-grip strength in pa...
peer reviewedThe field of translational research in Duchenne muscular dystrophy (DMD) has been trans...
Item does not contain fulltextThe field of translational research in Duchenne muscular dystrophy (DM...
OBJECTIVE: The main aim was to explore the changes in hand-grip strength in patients with Duchenne m...
INTRODUCTION: Duchenne muscular dystrophy (DMD) subjects ≥5 years with nonsense mutations were follo...
The development of new therapeutic agents for the treatment of Duchenne muscular dystrophy has put a...
The timed 4-stair climb (4SC) assessment has been used to measure function in Duchenne muscular dyst...
Duchenne muscular dystrophy (DMD) is a progressive X-linked genetic neuromuscular disorder that prim...
Contains fulltext : 174808.pdf (publisher's version ) (Open Access)BACKGROUND: The...
This study aimed to investigate possible asymmetries and relationships between performance of domina...
Duchenne muscular dystrophy is a rare genetic disorder with life-limiting pathology. Drisapersen ind...