Titlebook: Neuromuscular Diseases; A Practical Approach Michael Swash,Martin Schwartz Book 19882nd edition Springer-Verlag Berlin Heidelberg 1988 Neur

辞职

Diseases of Anterior Horn Cellse are usually limited to the anterior horn cells, but in adults other parts of the motor system, i.e. the upper motor neuron may be involved. The latter are classified as motor neuron disease, a disorder which is very rare in childhood. Certain viruses, particularly poliomyelitis, show a predilectio

后来

敏捷

Nerve Entrapment and Compression Syndromes and Other Mononeuropathiesury to the ulnar nerve at the elbow, or to the common peroneal nerve at the lateral aspect of the knee. More severe injury, or more prolonged compression or entrapment of nerves will lead, however, to more pronounced and less transient sensory disturbance and weakness in the distribution of the affe

柔美流畅

Brachial and Lumbar Nerve Root and Plexus Lesionsnitial symptoms of root lesions are nearly always sensory, consisting of paraesthesias and dysaesthesias in a radicular distribution. These sensory symptoms are often related to particular postures or activities. Radicular pain may be a major feature. Motor disability develops later and consists of

MEEK

Genetically Determined Neuropathiesinantly motor in type, is associated with deformities of the feet, particularly pes cavus. This group of disorders (Table 10.1) contains diseases inherited as an autosomal dominant or recessive trait and there may be a number of associated congenital anomalies. These disorders can often be recognise

dominant

Acquired Polyneuropathiesuent. About half of all insulin-dependent diabetics have symptomatic neuropathy, representing about 0.5% of the population of developed countries (Brown and Greene 1984; Brown and Asbury 1984) (Table 11.1).

CRAMP

脆弱带来

Inflammatory Myopathiesnd pathological features suggestive of inflammation. The inflammatory myopathies, as a group of disorders, are the commonest of the acquired myopathies. Characteristically, muscular involvement is widespread but in other cases muscles are involved in a focal or localised distribution. Acute, subacut

乐意

Muscular Dystrophiesrogressive degenerative changes in muscle fibres, without primary abnormality in the lower motor neuron. They are classified according to their clinical, morphological and genetic characteristics (see Chap. 5).

spinal-stenosis

er 3500 steroid glycosides, offering the structures and the data of the naturally occurring glycosides of steroids. All compounds are arranged according to the structure of the aglycone, and, in its own class, according to the increasing molecular weight, making Spectroscopic Data of Steroid Glycosi