Stroke is a common, serious, and disabling global health-care problem, and rehabilitation is
a major part of patient care. There is evidence to support rehabilitation in well coordinated …

Summary Charcot–Marie–Tooth disease is the most common inherited neuromuscular
disorder. There have been substantial advances in elucidating the molecular bases of this …

Abstract PMP22 related neuropathies comprise (1) PMP22 duplications leading to Charcot-
Marie-Tooth disease type 1A (CMT1A),(2) PMP22 deletions, leading to Hereditary …

Custom‐made foot orthoses for the treatment of foot pain - Hawke, F - 2008 | Cochrane Library
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Limb contractures are a common impairment in neuromuscular diseases. They contribute to
increased disability from decreased motor performance, mobility limitations, reduced …

Background: Duchenne muscular dystrophy (DMD) leads to progressive impairment of
muscle function, respiratory failure and premature death. Longitudinal data on the course of …

Abstract The Charcot–Marie–Tooth disease (CMT) causes significant muscular deficits in the
affected patients, restricts daily activities (ADL), and involves a severe disability. Although …

Charcot-Marie-Tooth (CMT) disease is the most frequent inherited neuropathy, affecting
1/1500 to 1/10000. CMT1A represents 60%-70% of all CMT and is caused by a duplication …

For patients diagnosed with a rare musculoskeletal or neuromuscular disease, pain may
transition from acute to chronic; the latter yielding additional challenges for both patients and …

Charcot–Marie–Tooth (CMT) disease is the most common inherited neuropathy and one of
the most common inherited diseases in humans. The diagnosis of CMT is traditionally made …