نتایج جستجو برای: paraplegia
تعداد نتایج: 4533 فیلتر نتایج به سال:
nethertons syndrome consists of the combination of ichthyosis, eczema, and abnormal hair and presents within the first 10 days of life with erythroderma. other reported features are short stature, mental retardation, and seizures. allergy to nuts and fish is also common amongst patients. mutations in the spink5 gene on 5q are reported in patients with nethertons syndrome. to the best of our kno...
Paraplegia leads to immobilisation associated with profound changes in body composition. The potential risks involved with these changes i.e. loss of lean tissue mass (LM) and bone mineral density (BMD) vs. gain in fat mass (FM) in body composition have implications for the health of the disabled individuals [1]. Body fat has been identified as a significant predictor of mortality in humans mak...
BACKGROUND Current treatment for extensive thoracoabdominal aortic aneurysms (TAAAs) involves high-risk surgical and endovascular repairs, with a hospital mortality exceeding 20%, and a postoperative paraplegia rate beyond 10.5%. OBJECTIVES The aim of this study was to present an estimation of the economic impacts of surgical and endovascular treatments of types II and III TAAAs in the US as ...
Studies with animal models are providing new insights into the pathology of hereditary spastic paraplegia, particularly how mutations in multiple, converging pathways can lead to this family of neuropathies.
The hereditary spastic paraplegias are a group of neurodegenerative conditions that all share the principal clinical feature of progressive lower limb spastic paralysis, caused by either failure of development or progressive degeneration of the corticospinal tract. The conditions are characterised by extreme genetic heterogeneity, with at least 20 genes involved. Until recently, no functional o...
This paper is based on study over twelve and a half years of 170 patients suffering from traumatic paraplegia or tetraplegia, ofwhom 162 survived for more than a month after injury, and of 103 patients with other lesions of the spinal cord. The patients in the second group were less suitable for analysis because in many the lesions were disseminated or incomplete: few could be compared with the...
Hereditary spastic paraplegia (HSP) or Strümpell-Lorrain syndrome is a heterogeneous group of inherited disorders, with prevalence ranged from 4.3 to 9.6 cases per 100,000 population. A common feature of these disorders is the slowly progressive and often severe spasticity, noticeably especially in the low limbs. Conventionally, HSP is divided into two clinical groups, uncomplicated (pure spast...
[This corrects the article on p. e98 in vol. 2, PMID: 27606357.].
Physiology There is little difference of opinion on the main physiological points. The micturition centre in the sacral cord, opposite the twelfth dorsal and first lumbar vertebral bodies, controls the normal filling of the bladder, reacts to a stretch in the muscle and empties the bladder, though perhaps not quite completely, in one sustained contraction. The afferent and efferent impulses pas...
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