Results 251 to 260 of about 161,013 (302)
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Defending against cerebellar disease
Journal of Neurophysiology, 2022A hedge fund billionaire’s children are suffering from cerebellar disease. He invited a group of neuroscientists to plan a search for therapies. What resulted is the outline of an implantable neural emulator that might electronically replace the damaged part of the brain.
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1997
This chapter analyzes the neuropsychological deficits in inherited cerebellar diseases and compares their symptomatology with animal models in which the exact anatomical localization of degeneration is known and limited to the cerebellum. Both animal and human data suggest that cerebellar cortical atrophy affects functions of the frontal lobe system ...
C W, Wallesch, C, Bartels
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This chapter analyzes the neuropsychological deficits in inherited cerebellar diseases and compares their symptomatology with animal models in which the exact anatomical localization of degeneration is known and limited to the cerebellum. Both animal and human data suggest that cerebellar cortical atrophy affects functions of the frontal lobe system ...
C W, Wallesch, C, Bartels
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Cerebellar Disease of Ruminants
Veterinary Clinics of North America: Food Animal Practice, 2017Cerebellar disease can be congenital or acquired. Clinical signs of cerebellar disease include hypermetric gait in all limbs, normal to increased muscle tone, wide-based stance, swaying, intention tremor, and convulsions. Vestibular signs may be observed.
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Cerebellar Ataxia Rehabilitation Trial in Degenerative Cerebellar Diseases
Neurorehabilitation and Neural Repair, 2011Objective. To investigate short- and long-term effects of intensive rehabilitation on ataxia, gait, and activities of daily living (ADLs) in patients with degenerative cerebellar disease. Methods. A total of 42 patients with pure cerebellar degeneration were randomly assigned to the immediate group or the delayed-entry control group.
Ichiro, Miyai +7 more
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Clinical Manifestations of Cerebellar Disease
Neurologic Clinics, 2014Clinical manifestations of cerebellar disease include ataxia and tremor, as well as nystagmus, dysarthria, and cognitive dysfunction. Recognition of the cerebellar pattern of disease can aid in the prompt and correct diagnosis and lead to appropriate treatment and rehabilitation to minimize disability.
Vijayakumar, Javalkar +2 more
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Cerebellar Disease in Infectious Mononucleosis
Archives of Neurology, 1966INFECTIOUS mononucleosis has perplexed the clinician with a myriad of signs, symptoms, and complications. We describe an unusual patient in his presenting form and subsequent course. The first report of infectious mononucleosis in 1885 by Filatoff 1 * classified the disease as a juvenile cervical adenitis, an infectious disease of childhood.
M D, Dowling, E J, Van Slyck
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Ocular Signs of Cerebellar Disease
Archives of Ophthalmology, 1982Ocular signs of cerebellar disease have been increasingly appreciated with the advent of means for quantitative recording of eye movements. The graphs in this article illustrate ocular flutter, dysmetria, abnormal (nonsmooth) pursuit, instability of fixation, faulty vestibular suppression, impaired optokinetic response, end-position nystagmus, and ...
D G, Cogan, F C, Chu, D B, Reingold
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Cerebellar Diseases and Occupation
AHFE International, 2020Cerebellar degenerative disorders are neurological diseases that may result in functional difficulties affecting autonomy and employability. Besides being a personal problem, cerebellar diseases are also a social issue in terms of costs incurred by the national health system and in the employment sphere.
Alberto Ranavoloa +12 more
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Crossed Cerebellar Diaschisis in Alzheimer’s Disease
Current Alzheimer Research, 2018Background: We describe the phenomenon of crossed cerebellar diaschisis (CCD) in four subjects diagnosed with Alzheimer’s disease (AD) according to the National Institute on Aging - Alzheimer Association (NIA-AA) criteria, in combination with 18F-FDG PET and 11C-PiB PET imaging.
Reesink, F.E. +10 more
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Cerebellar atrophy in Huntington's disease
Journal of the Neurological Sciences, 1981The clinical features are outlined and the neuropathological changes described in 3 cases (2 adults and 1 child) of Huntington's disease with severe atrophy of the cerebellum. Onset occurred at the ages of 56, 55 and 3 and death at 70, 62 and 6 years, respectively.
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