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Feasibility and safety of training with an exoskeletal robotic device for Japanese individuals with spinal cord injuries: a retrospective study. [PDF]
Asai N, Yokoyama O, Murata T.
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Clinical and systemic factors associated with pressure ulcer development: a retrospective evaluation of 339 patients in a palliative care unit. [PDF]
Kaya FO, Şimşek S.
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Paraplegia after coeliac plexus block [PDF]
M. Woodham, Magdi Hanna
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Journal of the American Medical Association, 1934
Spastic paraplegia is a descriptive term and not a diagnosis. Its causes are many. In the classic form it is characterized by a progressive spasticity in the lower limbs, with all the signs and symptoms of a pyramidal tract disease below the level of the lesion. The onset is described by the patient in terms of fatigability of the lower limbs.
N. W. Winkelman, John L. Eckel
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Spastic paraplegia is a descriptive term and not a diagnosis. Its causes are many. In the classic form it is characterized by a progressive spasticity in the lower limbs, with all the signs and symptoms of a pyramidal tract disease below the level of the lesion. The onset is described by the patient in terms of fatigability of the lower limbs.
N. W. Winkelman, John L. Eckel
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The Journal of Bone and Joint Surgery. British volume, 1967
1. A comparison of the results of sixty patients with Pott's paraplegia, half operated upon and half treated conservatively, showed that better results were achieved in a much shorter time in those treated surgically. 2. Extra-pleural antero-lateral decompression is the operation of choice in cases of Pott's paraplegia. 3.
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1. A comparison of the results of sixty patients with Pott's paraplegia, half operated upon and half treated conservatively, showed that better results were achieved in a much shorter time in those treated surgically. 2. Extra-pleural antero-lateral decompression is the operation of choice in cases of Pott's paraplegia. 3.
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Neurologic Clinics, 2002
The hereditary spastic paraplegias (HSPs) comprise a large group of inherited neurologic disorders. HSP is classified according to the mode of inheritance, the HSP locus when known, and whether the spastic paraplegia syndrome occurs alone or is accompanied by additional neurologic or systemic abnormalities.
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The hereditary spastic paraplegias (HSPs) comprise a large group of inherited neurologic disorders. HSP is classified according to the mode of inheritance, the HSP locus when known, and whether the spastic paraplegia syndrome occurs alone or is accompanied by additional neurologic or systemic abnormalities.
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Emergency Medicine Journal, 2018
A 75-year-old man presented with acute onset thoracic back pain, progressive leg weakness with numbness and urinary retention. His symptoms started suddenly and progressed overnight. He denied a recent history of trauma. On neurological examination he had complete loss of all sensations below Th10 level and leg paraplegia (American Spinal Injury ...
Adomas Bunevicius +2 more
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A 75-year-old man presented with acute onset thoracic back pain, progressive leg weakness with numbness and urinary retention. His symptoms started suddenly and progressed overnight. He denied a recent history of trauma. On neurological examination he had complete loss of all sensations below Th10 level and leg paraplegia (American Spinal Injury ...
Adomas Bunevicius +2 more
openaire +2 more sources

