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Quantification of HTLV-I proviral load in experimentally infected rabbits [PDF]

Tong-Mao Zhao, Bishop Hague, David L Caudell, R Mark Simpson, Thomas J Kindt   +4 more
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The neuropathology of hereditary spastic paraparesis

Clinical Neurology and Neurosurgery, 1992
Hereditary spastic paraparesis or Strümpell's disease is a genetically determined neurodegenerative disorder in which the signs and symptoms are predominant in the legs. Inheritance is usually autosomal dominant and in a minority recessive. Neuropathological study reveals a degeneration of the corticospinal tract decreasing from lower lumbar to ...
exaly   +3 more sources

Hereditary spastic paraparesis

Clinical Neurology and Neurosurgery, 1993
R.P.M. Bruyn, J. van Deutekom, R.R. Frants, G.W. Padberg   +3 more
exaly   +2 more sources

No association of spastic paraparesis genes in PSEN1 Alzheimer's disease with spastic paraparesis

NeuroReport, 2007
Familial Alzheimer's disease due to presenilin 1 (PSEN1) mutations shows considerable phenotypic variability with differences in neuropathology and neurological symptoms. Spastic paraparesis is a common neurological phenotype associated with Alzheimer's disease arising from PSEN1 mutations.
Helena, Karlstrom, John B J, Kwok, Gillian C, Gregory, Marianne, Hallupp, William S, Brooks, Peter R, Schofield   +5 more
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The Neurourology of Tropical Spastic Paraparesis

British Journal of Urology, 1991
Summary— We report the clinical features, urodynamic results and neurophysiological findings in 6 patients with urinary symptoms related to tropical spastic paraplegia. The widespread nature of the pathological changes within the nervous system result in a complex variety of urodynamic and neurophysiological ...
I, Eardley, C J, Fowler, K, Nagendran, R S, Kirby, P, Rudge   +4 more
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Tropical spastic paraparesis

2023
A large number of causative agents can result in spinal cord disorders in the tropics including etiologies similar to those of temperate regions such as trauma, spinal bone and disc lesions, tumors, epidural abscess, and congenital malformations. Yet infectious and nutritional disorders differ in their higher prevalence in tropical regions including ...
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Tropical spastic paraparesis in an Aborigine

Medical Journal of Australia, 1993
To present the first documented case of human T-lymphotropic virus type I (HTLV-I) associated myelopathy/tropical spastic paraparesis in the Australian population.A 31-year-old Aboriginal man with an 18-month history of progressive weakness of the legs was found to have an upper motor neurone weakness of all limbs associated with sphincteric ...
N, Rajabalendaran, R, Burns, L C, Mollison, W, Blessing, M G, Kirubakaran, P, Lindschau   +5 more
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Hereditary spastic paraparesis and psychosis

European Journal of Neurology, 2006
Hereditary spastic paraparesis (HSP) is characterized by progressive spasticity and weakness of the legs with or without additional abnormalities. Reports of psychiatric disorders in patients with HSP are limited to mood disturbances rather than to psychosis. We had noted significant psychotic illness in several patients recruited to a survey of HSP in
P, McMonagle, M, Hutchinson, B, Lawlor
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Familial spastic paraparesis

Neurology, 1985
Adrenoleukodystrophy (ALD) must be considered in the diagnosis of men with progressive nervous system disease. We found the biochemical defect characteristic of ALD in two brothers with spastic paraparesis of late adult onset. Family study then revealed other affected men and asymptomatic heterozygotes in a pattern that conformed to an X-linked pattern
B P, O'Neill, J W, Swanson, F R, Brown, J W, Griffin, H W, Moser   +4 more
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