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The Neuropathology of Huntington’s Disease: Classical Findings, Recent Developments and Correlation to Functional Neuroanatomy: Advances in Anatomy, Embryology and Cell Biology, cartea 217

Autor Udo Rüb, Jean Paul G. Vonsattel, Helmut Heinsen, Horst-Werner Korf
en Limba Engleză Paperback – 8 oct 2015
This monograph describes the progress in neuropathological HD research made during the last century, the neuropathological hallmarks of HD and their pathogenic relevance. Starting with the initial descriptions of the progressive degeneration of the striatum as one of the key events in HD, the worldwide practiced Vonsattel HD grading system of striatal neurodegeneration will be outlined. Correlating neuropathological data with results on the functional neuroanatomy of the human brain, subsequent chapters will highlight recent HD findings: the neuronal loss in the cerebral neo-and allocortex, the neurodegeneration of select thalamic nuclei, the affection of the cerebellar cortex and nuclei, the involvement of select brainstem nuclei, as well as the pathophysiological relevance of these pathologies for the clinical picture of HD. Finally, the potential pathophysiological role of neuronal huntingtin aggregations and the most important and enduring challenges of neuropathological HD research are discussed.
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Specificații

ISBN-13: 9783319192840
ISBN-10: 3319192841
Pagini: 146
Ilustrații: XIV, 146 p. 50 illus., 47 illus. in color.
Dimensiuni: 155 x 235 x 10 mm
Greutate: 0.33 kg
Ediția:1st ed. 2015
Editura: Springer International Publishing
Colecția Springer
Seria Advances in Anatomy, Embryology and Cell Biology

Locul publicării:Cham, Switzerland

Public țintă

Research

Cuprins

1. Introduction.- 2. The neuropathological grading of Huntington disease.- 3. The cerebral cortex in Huntington´s disease.- 4. Degeneration of select motor and limbic nuclei of the thalamus in Huntington’s disease.- 5. Consistent and widespread degeneration of the cerebellum in Huntington’s disease.- 6. Elucidation of the role of the premotor oculomotor brainstem nuclei in the pathogenesis of oculomotor dysfunctions in Huntington’s disease.- 7. Widespread brainstem neurodegeneration in Huntington’s disease.- 8. Intraneuronal transport and defense mechanisms with possible pathogenetic relevance in Huntington’s disease.- 9. The disease protein huntingtin and neuronal protein aggregations in Huntington’s disease.- 10. Pathological nerve cell alterations in Huntington’s disease (HD) and their possible role for the demise of nerve cells.- 11. Conclusions and outlook.

Recenzii

“This multiauthored monograph is a comprehensive overview of Huntington’s disease by experts in this field. … The photographs are of consistently high quality. The captions are complete and accurate. … For a basic scientist, neurologist, neuropathologist, or anyone with an interest in neurodegenerative disease, this book provides a thorough review and authoritative update on Huntington’s disease. It is a reliable resource and a complete academic delight.” (Sherry Krawitz, Doody’s Book Reviews, March, 2016)

Textul de pe ultima copertă

This monograph describes the progress in neuropathological HD research made during the last century, the neuropathological hallmarks of HD and their pathogenic relevance. Starting with the initial descriptions of the progressive degeneration of the striatum as one of the key events in HD, the worldwide practiced Vonsattel HD grading system of striatal neurodegeneration will be outlined. Correlating neuropathological data with results on the functional neuroanatomy of the human brain, subsequent chapters will highlight recent HD findings: the neuronal loss in the cerebral neo-and allocortex, the neurodegeneration of select thalamic nuclei, the affection of the cerebellar cortex and nuclei, the involvement of select brainstem nuclei, as well as the pathophysiological relevance of these pathologies for the clinical picture of HD. Finally, the potential pathophysiological role of neuronal huntingtin aggregations and the most important and enduring challenges of neuropathological HD research are discussed.

Caracteristici

Describes the progress made during more than hundred years of neuropathological HD research, the neuropathological hallmarks of HD and their pathogenic and clinical relevance Explains the potential pathophysiological role of axonal transport deficits and impairments of the neuronal protein quality control machinery in the disease process Illustrates the potential pathophysiological role of neuronal huntingtin aggregations and nerve cell alterations, as well as the possible significance of transneuronal mechanisms for the spread of the neurodegenerative process of HD