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Dietary and lifestyle interventions for the management of hereditary ataxias. [PDF]
Front NutrYang W, Thompson B, Kwa FAA.
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The Indian Journal of Pediatrics, 1962
A brief review of spinocerebellar degenerations as seen in pediatric practive with four illustrative case reports is presented.
R K, CHANDRA, S K, KHETARPAL, O P, GHAI
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A brief review of spinocerebellar degenerations as seen in pediatric practive with four illustrative case reports is presented.
R K, CHANDRA, S K, KHETARPAL, O P, GHAI
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Expert Opinion on Pharmacotherapy, 2003
The spinocerebellar ataxias (SCA) are a large group of inherited disorders affecting the cerebellum and its afferent and efferent pathways. Their hallmark symptom is slowly progressive, symmetrical, midline, and appendicular ataxia. Some may also have associated hyperkinetic movements (chorea, dystonia, myoclonus, postural/action tremor, restless legs,
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The spinocerebellar ataxias (SCA) are a large group of inherited disorders affecting the cerebellum and its afferent and efferent pathways. Their hallmark symptom is slowly progressive, symmetrical, midline, and appendicular ataxia. Some may also have associated hyperkinetic movements (chorea, dystonia, myoclonus, postural/action tremor, restless legs,
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Slow Saccades in Spinocerebellar Degeneration
Archives of Neurology, 1976Two patients with spinocerebellar degeneration made abnormally slow horizontal refixations. One patient produced quick phases of nystagmus with identical maximum velocities, suggesting her refixations were abnormal saccades and not voluntary pursuit movements.
D S, Zee +4 more
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Spinocerebellar degeneration (SCD): cognitive disturbances
Acta Neurologica Scandinavica, 1991The performance of 30 patients younger than 65 years with spinocerebellar degeneration (SCD) was compared with control subjects matched for age, sex, and education in standardized neuropsychological tests. SCD patients exhibited abnormalities in WAIS, in the recall test of anterograde verbal memory, in verbal fluency, in visuospatial function and on ...
N, Hirono +4 more
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Adrenoleukodystrophy Presenting as Spinocerebellar Degeneration
European Neurology, 1989The clinical features of 3 patients from a kindred with adrenoleukodystrophy and the analysis of their plasma sphingomyelin are described. Onset of symptoms was between the ages of 33 and 54 years. Ataxic gait and spasticity were the only symptoms noted during the early stage of the disorder. Dementia and optic atrophy were present in two of the cases.
T, Nakazato +4 more
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Peripheral neuropathy in spinocerebellar degenerations
Muscle & Nerve, 1981AbstractNerve conduction studies have been performed in 19 subjects with hereditary spinocerebellar degenerations other than Friedreich ataxia. Clinically, they may be classified as olivopontocerebellar atrophy or cerebello‐olivary degeneration. In 9 patients, sensory conduction was abnormal, and in the whole group there was a significant impariment of
J G, McLeod, W A, Evans
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Mitochondrial dysfunction and spinocerebellar degenerations
Neurochemical Pathology, 1986A simplified classification of the spinocerebellar degenerations is proposed. Axonal ataxias include Friedreich's ataxia and other conditions involving, primarily, neurons with very long axons. Multiple system degenerations include the various olivopontocerebellar atrophies and related disorders.
J M, Cedarbaum, J P, Blass
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