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 …

Anoctaminopathy-5 refers to a group of hereditary skeletal muscle or bone disorders due to
mutations in the anoctamin 5 (ANO5)-encoding gene, ANO5. ANO5 is a 913-amino acid …

Introduction: It has not been established whether progressive resistance training (PRT) and
aerobic training (AT) are feasible and efficient in myasthenia gravis (MG). Methods: Fifteen …

Objective: To investigate the effect of regular aerobic training and postexercise protein-
carbohydrate supplementation in patients with facioscapulohumeral muscular dystrophy …

Different genetic mutations underlying distinct pathogenic mechanisms have been identified
as cause of muscle fibers degeneration and strength loss in limb girdle muscular …

Purpose: Exoskeletons have been developed for rehabilitation of patients with walking
impairment due to neurological disorders. Recent studies have shown that the voluntary …

Background: The benefit and safety of exercise training for patients with neuromuscular
disorders (NMDs) has long been a contentious topic. This is, in part, due to recognised …

In muscle diseases different molecular mechanisms are responsible, by distinct cellular
pathways, of muscle fibers contraction insufficiency and exercise intolerance. Depending on …

Anoctamin-5 related muscle disease is caused by biallelic pathogenic variants in the
anoctamin-5 gene (ANO5) and shows variable clinical phenotypes: limb-girdle muscular …

Limb-girdle muscular dystrophy (LGMD) poses unique challenges for women during
pregnancy, necessitating comprehensive care and tailored management strategies. The …