Endurance training: an effective and safe treatment for patients with LGMD2I

scientific article published on 01 January 2007

Endurance training: an effective and safe treatment for patients with LGMD2I is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1212/01.WNL.0000250358.32199.24
P698PubMed publication ID17200494

P50authorThomas KragQ46658578
P2093author name stringVissing J
Hauerslev S
Jeppesen TD
Sveen ML
P433issue1
P304page(s)59-61
P577publication date2007-01-01
P1433published inNeurologyQ1161692
P1476titleEndurance training: an effective and safe treatment for patients with LGMD2I
P478volume68

Reverse relations

cites work (P2860)
Q34745089A novel in vitro model for studying quiescence and activation of primary isolated human myoblasts
Q35890267Aerobic Training in Patients with Congenital Myopathy
Q42585723Aerobic exercise in children with oxidative phosphorylation defects
Q37589572Autonomic dysfunction in muscular dystrophy: a theoretical framework for muscle reflex involvement.
Q47625983Childhood Activity on Progression in Limb Girdle Muscular Dystrophy 2I.
Q38634370Clinical Trials in Spinal and Bulbar Muscular Atrophy-Past, Present, and Future
Q34872181Efficacy of muscle exercise in patients with muscular dystrophy: a systematic review showing a missed opportunity to improve outcomes.
Q38639343Exercise Therapy in Spinobulbar Muscular Atrophy and Other Neuromuscular Disorders.
Q37678217Exercise biology and medicine: innovative research to improve global health
Q92863877Exercise therapy for muscle and lower motor neuron diseases
Q92863880Exercise therapy in muscle diseases: open issues and future perspectives
Q48613716FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies
Q37014708Moderate-intensity treadmill running promotes expansion of the satellite cell pool in young and old mice
Q35774675Muscle exercise in limb girdle muscular dystrophies: pitfall and advantages.
Q37899974Neurotoxic effects of androgens in spinal and bulbar muscular atrophy.
Q92487786Nutrition and exercise in Pompe disease
Q36218715Pathophysiology of protein aggregation and extended phenotyping in filaminopathy
Q82621506Physiotherapy, based on the Bobath concept, may influence the gait pattern in persons with limb‐girdle muscle dystrophy: a multiple case series study
Q37165223Safety and efficacy of a 6-month home-based exercise program in patients with facioscapulohumeral muscular dystrophy: A randomized controlled trial
Q42002252Single-Blind, Randomized, Controlled Clinical Trial of Exercise in Ambulatory Spinal Muscular Atrophy: Why are the Results Negative?
Q24201278Strength training and aerobic exercise training for muscle disease
Q24240846Strength training and aerobic exercise training for muscle disease
Q33683997The chondrogenic response to exercise in the proximal femur of normal and mdx mice
Q81826532The physiological effects of IGF-1 (class 1:Ea transgene) over-expression on exercise-induced damage and adaptation in dystrophic muscles of mdx mice
Q37329558Therapeutic possibilities in the autosomal recessive limb-girdle muscular dystrophies
Q41334112Treadmill Training with HAL Exoskeleton-A Novel Approach for Symptomatic Therapy in Patients with Limb-Girdle Muscular Dystrophy-Preliminary Study
Q84199391[Standard treatment for myositis and muscular dystrophies]

Search more.