Results 151 to 160 of about 10,460 (201)

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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Hereditary spastic paraparesis

Clinical Neurology and Neurosurgery, 1993
R P M Bruyn, R R Frants, G W Padberg
exaly   +2 more sources

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 ...
openaire   +2 more sources

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
openaire   +2 more sources

Genetic Mapping to 10q23.3-q24.2, in a Large Italian Pedigree, of a New Syndrome Showing Bilateral Cataracts, Gastroesophageal Reflux, and Spastic Paraparesis with Amyotrophy

American Journal of Human Genetics, 1999
We have recently observed a large pedigree with a new rare autosomal dominant spastic paraparesis. In three subsequent generations, 13 affected individuals presented with bilateral cataracts, gastroesophageal reflux with persistent vomiting, and spastic ...
Marco Seri, Roberto Cusano, Paola Forabosco   +2 more
exaly   +2 more sources

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
openaire   +2 more sources

Progressive Spastic Paraparesis

Archives of Neurology, 1977
To the Editor.— Relative to the article "Progressive Spastic Paraparesis and Adrenal Insufficiency" by Gumbinas and associates published in the October issue of theArchives(33:678, 1976), I take the liberty to add that in the article "Atrophie idiopathique des surrenales et sclerose combinee de la moelle epiniere" by M. Bedivan, A.
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Spastic paraparesis and sensory neuropathy

Muscle & Nerve, 1992
A 12-year-old developed a slowly progressive spastic gait at the age of 3. A marked loss of pain and temperature sensations led to a mutilating acropathy starting at age 5. Electrodiagnostic studies revealed a symmetric, axonal, predominantly sensory neuropathy, and magnetic resonance imaging ruled out compression of spinal cord.
S N, Tenembaum, R C, Reisin, A L, Taratuto, N, Fejerman   +3 more
openaire   +2 more sources