Titlebook: Spinal Cord Disease; Basic Science, Diagn Edmund Critchley,Andrew Eisen,Michael Swash Book 1997 The Editor(s) (if applicable) and The Autho

移植

Congruous

E. M. R. Critchley,M. T. Isaac search for coronary lesions, in the asymptomatic general population, does not seem reasonable. Lesions will often be found but will not necessarily be affecting myocardial perfusion in a significant way. Preservation of perfusion relates to other factors, including (1) the capacity of coronary vess

STELL

G. R. Critchleyytical and pathophysiological and functional charac­ statistical point of view. This approach is ter. For adequate experimental or clinical required for correct decision-making. interpretation, such information should This book is therefore the result of necessarily be interpreted alongside the accu

傲慢人

Prospects for Spinal Cord Repair after Injury, who suffer SCI are male (82%) and between 16 and 30 years of age (61%) (Tator et al. 1993). In the United States, motor vehicle accidents (48%), accidental falls (21%), sports injuries (14%) and gunshot wounds (15%) constitute the major causes of SCI.

NOTCH

Excitotoxin

Autonomic Dysfunction in Spinal Cord Disease, in the intermediolateral cell columns. This relative absence of .pathetic activation may lead to a relative overactivity of vagal activity especially if the functional disconnection is relatively acute and complete; an example is the occurrence of profound bradycardia and cardiac arrest with tracheal suction in the recently injured quadraplegic.

Fantasy

NICE

Spasticity,n may reveal a mixture of signs such as increased tone, clasp knife rigidity, loss of fine movements, brisk reflexes including spread of reflex activity, clonus and an upgoing plantar response. There may be spasms, both flexor and extensor, which may be spontaneous or precipitated by examination.

Shuttle

繁殖

Craniocervical Anomalies and Non-traumatic Syringomyelia, found together in the same patient. There is also little genuine consensus of opinion about the cause of the anomalies or of related syringomyelia. In this review we have attempted to shed a little light by considering first the anomalies themselves and then proceeding to a more detailed discussion of syringomyelia and its surgical management.