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Lipofuscin in Amyotrophic Lateral Sclerosis
Archives of Neurology, 1984Lipofuscin has been reported to accumulate in abnormal amounts in motor neurons of patients with amyotrophic lateral sclerosis (ALS). Microdensitometry was used to quantitate such lipid masses in spinal motor neurons in normal subjects compared with spinal motor neurons in ALS cases.
G B, McHolm, M J, Aguilar, F H, Norris
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Amyotrophic Lateral Sclerosis Model
2018Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that affects upper and lower motor neurons in the brain and the spinal cord. Due to the progressive neurodegeneration, ALS leads to paralysis and death caused by respiratory failure 2-5 years after the onset of symptoms. There is no effective cure available.
Yumiko, Azuma +3 more
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Thermoregulation in amyotrophic lateral sclerosis
2018Amyotrophic lateral sclerosis (ALS) is the major adult-onset motor neuron disease, and is clinically, pathologically, and genetically associated with frontotemporal dementia, the second cause of dementia in the elderly. Here, we review the evidence linking thermoregulation and ALS.
Dupuis, Luc +2 more
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Home Healthcare Nurse: The Journal for the Home Care and Hospice Professional, 1985
W K, Beebe, K, Gomez
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W K, Beebe, K, Gomez
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