Latest papers

Unexpected myopathy associated with a mutation in MYBPC3 and misplacement of the cardiac myosin binding protein C.

An integrated approach to the diagnosis of muscle disorders: what is the role of muscle imaging?

Extensive muscle necrosis and infection following treatment of a lower extremity vascular malformation with Sotradecol and absolute ethanol.

Exertional compartment syndrome.

Diabetic myopathy: MRI patterns and current trends.

[Critical illness myopathy. Neurophysiological and muscular biopsy assessment in 33 patients]

Individualising the risks of statins in men and women in England and Wales: population-based cohort study.

Assessment of pelvic floor muscle function in women with and without low back pain using transabdominal ultrasound.

Can inhalation agents be used in the presence of a child with myopathy?

[Diaphragmatic diseases].

Pain channelopathies.

Muscle channelopathies: does the predicted channel gating pore offer new treatment insights for hypokalaemic periodic paralysis?

Voltage-sensor mutations in channelopathies of skeletal muscle.

[Endophytes possibly the cause of atypical myopathy]

A myopathy-linked tropomyosin mutation severely alters thin filament conformational changes during activation.

Calsequestrin and junctin immunoreactivity in hexagonally cross-linked tubular arrays myopathy.

Epidemiology of myosteatosis.

166th ENMC International Workshop on Collagen type VI-related Myopathies, 22-24 May 2009, Naarden, The Netherlands.

Two Australian families with inclusion-body myopathy, Paget's disease of bone and frontotemporal dementia: novel clinical and genetic findings.

In vitro analysis of rod composition and actin dynamics in inherited myopathies.