Background Strength training or aerobic exercise programmes, or both, might optimise
muscle and cardiorespiratory function and prevent additional disuse atrophy and …

Muscle and lower motor neuron diseases share a common denominator of perturbed
muscle function, most often related to wasting and weakness of muscles. This leads to a …

Background Myotonic dystrophy type 1 is the most common form of muscular dystrophy in
adults and leads to severe fatigue, substantial physical functional impairment, and restricted …

Background Myotonic dystrophy type 1 (DM1) is a neuromuscular disease characterized by
multisystemic involvements including a progressive loss of maximal muscle strength and …

MiR-1 and myostatin are markers for muscle growth and regeneration. Myostatin has a key
role in the regulation of muscle mass. Myotonic dystrophy type 1 (DM1) patients have a …

Physical modalities are tools that can be used to complement a patient's rehabilitation
treatment plan through the use of thermal, sound, electrical, and light energy. They can be …

Muscular dystrophy (MD) is a group of neuromuscular diseases characterized by
progressive muscle weakness due to various mutations in several genes involved in muscle …

The reviewed studies extend previous knowledge about exercise, indicating that exercise is
generally safe and well tolerated, and improves functional outcomes in patients with …

Objective To examine the evidence regarding FES-cycling's physiological and clinical
effects. Data Sources The study was conducted in accordance with PRISMA. PubMed …

Abstract Myologists working in Padua (Italy) were able to continue a half-century tradition of
studies of skeletal muscles, that started with a research on fever, specifically if and how …