The value of quantitative MR methods as potential biomarkers in neuromuscular disease is being increasingly recognized. Previous studies of the magnetization transfer ratio have demonstrated sensitivity to muscle disease. The aim of this work was to investigate quantitative magnetization transfer imaging of skeletal muscle in healthy subjects at 3 T to evaluate its potential use in pathological...

Magnetic resonance imaging (MRI) studies of superior oblique (SO) muscles have revealed a high incidence of SO muscle atrophy/hypoplasia in congenital SO palsy patients. It has also been reported that long-standing acquired SO palsy patients show atrophic SO muscles in the affected eye. The purpose of this study was to compare the incidence of SO muscle atrophy/hypoplasia in congenital and acqu...

In a paper read in London to the Medical Society for the Study of Venereal Diseases in 1955 it was shown that of 1,000 consecutive patients with early syphilis and gonorrhoea, which were among those seen at the venereal diseases clinic of St. Mary's Hospital, London, in 1954, 84 (8-4 per cent.) admitted that they had been infected by homosexual contact (Jefferiss, 1956). A similar investigation...

the term ultra short is not clearly defined in ultrashort-segment hirschsprung’s disease. the limited extent of the ultrashort-segment hirschsprung’s disease allows for treatment with extended sphincteromyectomy. in anal sphincter achalasia, anal sphincter dilatation under general anesthesia may be sufficient to treat the condition; in cases with persistent constipation, sphincteromyectomy is i...

Muscle diseases can constitute a large variety of both acquired and hereditary disorders. Myopathies in systemic disease results from several different disease processes including endocrine, inflammatory, paraneoplastic, infectious, drug- and toxin-induced, critical illness myopathy, metabolic, and myopathies with other systemic disorders. Patients with systemic myopathies often present acutely...

Muscle diseases constitute a large variety of both acquired and hereditary disorders that can affect muscle structure, metabolism, or the function of the muscle channel. A successful clinical approach to a patient with a suspected myopathy is based on a thorough medical history and neurological examination. Associated clinical symptoms such as myoglobinuria, contractures, myotonia, cardiac dise...