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Non-dopamine Lesions in Parkinsons Disease
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2042146Non-dopamine Lesions in Parkinsons Diseasehttps://www.gandhi.com.mx/non-dopamine-lesions-in-parkinson-s-disease-1/phttps://gandhi.vtexassets.com/arquivos/ids/1260695/dbce135c-c6cb-4acc-997a-6fa7eeb2b7cc.jpg?v=63875508079773000025612845MXNOxford University PressInStock/Ebooks/<p>Parkinsons disease becomes apparent only after substantial loss (60) of the dopamine neurons in the substantia nigra. By this time there has already been widespread neural inclusion formation in the peripheral and central nervous system of patients with the disease, although this has only been recognized more recently. Degeneration in these widespread regions of the peripheral and central nervous system is now known to impact on disease symptoms, progression and treatment over time. This book aims to provide a comprehensive review of these non-dopamine lesions in Parkinsons disease by assessing our current knowledge of their presence and pathophysiology, how they relate to different symptoms and, where relevant, discuss how they may be potentially treated. The book addresses most of the known symptoms that occur in patients with Parkinsons disease. In addition to the classic motor triad, motor speech, eye movements, olfactory dysfunction, autonomic dysfunction, pain and sensory abnormalities, sleep disturbances, depression and apathy, dopamine dysregulation syndromes, hallucinations and psychoses, cognitive impairment and dementia, and systemic manifestations are all reviewed. Early selective cell loss in non-dopaminergic regions is highlighted (the glutamate projection neurons of the presupplementary motor cortex and caudal intralaminar thalamus) in addition to the widespread inclusion formation in many regions outside the basal ganglia that characterize the disease. Overall this book provides a comprehensive analysis of the lesions associated with the most common symptoms found in patients with Parkinsons disease.</p>...2002467Non-dopamine Lesions in Parkinsons Disease25612845https://www.gandhi.com.mx/non-dopamine-lesions-in-parkinson-s-disease-1/phttps://gandhi.vtexassets.com/arquivos/ids/1260695/dbce135c-c6cb-4acc-997a-6fa7eeb2b7cc.jpg?v=638755080797730000InStockMXN99999DIEbook20109780190208738_W3siaWQiOiIwN2RiMmMxYi0zYzk5LTRjOGMtOWE3My1hOTUxOTZiMmM1ODMiLCJsaXN0UHJpY2UiOjI4NDUsImRpc2NvdW50IjoyODQsInNlbGxpbmdQcmljZSI6MjU2MSwiaW5jbHVkZXNUYXgiOnRydWUsInByaWNlVHlwZSI6Ildob2xlc2FsZSIsImN1cnJlbmN5IjoiTVhOIiwiZnJvbSI6IjIwMjUtMDctMjJUMTE6MDA6MDBaIiwicmVnaW9uIjoiTVgiLCJpc1ByZW9yZGVyIjpmYWxzZX1d9780190208738_<p>Parkinsons disease becomes apparent only after substantial loss (>60) of the dopamine neurons in the substantia nigra. By this time there has already been widespread neural inclusion formation in the peripheral and central nervous system of patients with the disease, although this has only been recognized more recently. Degeneration in these widespread regions of the peripheral and central nervous system is now known to impact on disease symptoms, progression and treatment over time. This book aims to provide a comprehensive review of these non-dopamine lesions in Parkinsons disease by assessing our current knowledge of their presence and pathophysiology, how they relate to different symptoms and, where relevant, discuss how they may be potentially treated. The book addresses most of the known symptoms that occur in patients with Parkinsons disease. In addition to the classic motor triad, motor speech, eye movements, olfactory dysfunction, autonomic dysfunction, pain and sensory abnormalities, sleep disturbances, depression and apathy, dopamine dysregulation syndromes, hallucinations and psychoses, cognitive impairment and dementia, and systemic manifestations are all reviewed. Early selective cell loss in non-dopaminergic regions is highlighted (the glutamate projection neurons of the presupplementary motor cortex and caudal intralaminar thalamus) in addition to the widespread inclusion formation in many regions outside the basal ganglia that characterize the disease. Overall this book provides a comprehensive analysis of the lesions associated with the most common symptoms found in patients with Parkinsons disease.</p>(*_*)9780190208738_<p>Parkinsons disease becomes apparent only after substantial loss (60) of the dopamine neurons in the substantia nigra. By this time there has already been widespread neural inclusion formation in the peripheral and central nervous system of patients with the disease, although this has only been recognized more recently. Degeneration in these widespread regions of the peripheral and central nervous system is now known to impact on disease symptoms, progression and treatment over time. This book aims to provide a comprehensive review of these non-dopamine lesions in Parkinsons disease by assessing our current knowledge of their presence and pathophysiology, how they relate to different symptoms and, where relevant, discuss how they may be potentially treated. The book addresses most of the known symptoms that occur in patients with Parkinsons disease. In addition to the classic motor triad, motor speech, eye movements, olfactory dysfunction, autonomic dysfunction, pain and sensory abnormalities, sleep disturbances, depression and apathy, dopamine dysregulation syndromes, hallucinations and psychoses, cognitive impairment and dementia, and systemic manifestations are all reviewed. Early selective cell loss in non-dopaminergic regions is highlighted (the glutamate projection neurons of the presupplementary motor cortex and caudal intralaminar thalamus) in addition to the widespread inclusion formation in many regions outside the basal ganglia that characterize the disease. Overall this book provides a comprehensive analysis of the lesions associated with the most common symptoms found in patients with Parkinsons disease.</p>...9780190208738_Oxford University Presslibro_electonico_11264f87-e419-392c-aa8b-7025d6cf8635_9780190208738;9780190208738_9780190208738InglésMéxicohttps://getbook.kobo.com/koboid-prod-public/oxfordupuk-epub-325f8673-8e37-4f6a-ada5-913deeb932b4.epub2010-11-15T00:00:00+00:00Oxford University Press