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The neuroepidemiology of tropical spastic paraparesis
Annals of Neurology, 1988Recent neuroepidemiological studies of endemic tropical spastic paraparesis (TSP) have confirmed the existence of high-prevalence foci in several tropical islands, including Jamaica and Martinique in the Caribbean, Tumaco off the Pacific coast of Colombia, and the Seychelles in the Indian Ocean.
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Clonus Associated with Tropical Spastic Paraparesis
New England Journal of Medicine, 2016A 53-year-old woman with tropical spastic paraparesis reported several months of worsening weakness of the legs and feet. On examination, she had severe spasticity and weakness of both legs and feet, bilateral Babinski sign, and bilateral patellar clonus, shown in a video.
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2014
Hereditary spastic paraplegia (SPG) is a group of neurodegenerative disorders characterized by progressive spasticity and weakness of the lower limbs, resulting from “dying back” axonopathy of the corticospinal tract. Pure and complicated forms are known, and loci with autosomal dominant, recessive, and X-linked patterns of inheritance were identified.
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Hereditary spastic paraplegia (SPG) is a group of neurodegenerative disorders characterized by progressive spasticity and weakness of the lower limbs, resulting from “dying back” axonopathy of the corticospinal tract. Pure and complicated forms are known, and loci with autosomal dominant, recessive, and X-linked patterns of inheritance were identified.
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2014
Spastic paraplegia or paraparesis (SPG) is a group of genetically heterogeneous disorders, characterized predominantly by progressive lower extremity spasticity and weakness, with either autosomal dominant and recessive or X-linked pattern of inheritance. SPG is classified by mode of inheritance and whether the primary symptoms occur in isolation (pure
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Spastic paraplegia or paraparesis (SPG) is a group of genetically heterogeneous disorders, characterized predominantly by progressive lower extremity spasticity and weakness, with either autosomal dominant and recessive or X-linked pattern of inheritance. SPG is classified by mode of inheritance and whether the primary symptoms occur in isolation (pure
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The neuropathology of hereditary spastic paraparesis
Clinical Neurology and Neurosurgery, 1992Hereditary 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 ...
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Spastic paraplegia-paraparesis
Journal of the Neurological Sciences, 1980Julian Y. Ungar-Sargon +2 more
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