1927
DOI: 10.1001/archneurpsyc.1927.02210060002001
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Pathologic Changes in Huntington's Chorea

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Cited by 68 publications
(3 citation statements)
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“…These results are of considerable interest when contrasted with the effects of Parkinson's disease on synchronization, discussed above. In Huntington's chorea, the ganglion cells in the putamen and caudate nucleus are grossly reduced in number and may be absent; little or no loss of cells is seen in the globus pallidus, the final coordinating pathway of the basal ganglion or in the subsantia nigra (Dunlap, 1927). In Parkinson's disease, however, there is a marked depigmentation and cell degeneration, particularly in the pars compacta of the substantia nigra and also in the locus coeruleus (Oppenheimer, 1976).…”
Section: Basal Ganglia and Cerebellar Lesionsmentioning
confidence: 99%
“…These results are of considerable interest when contrasted with the effects of Parkinson's disease on synchronization, discussed above. In Huntington's chorea, the ganglion cells in the putamen and caudate nucleus are grossly reduced in number and may be absent; little or no loss of cells is seen in the globus pallidus, the final coordinating pathway of the basal ganglion or in the subsantia nigra (Dunlap, 1927). In Parkinson's disease, however, there is a marked depigmentation and cell degeneration, particularly in the pars compacta of the substantia nigra and also in the locus coeruleus (Oppenheimer, 1976).…”
Section: Basal Ganglia and Cerebellar Lesionsmentioning
confidence: 99%
“…Clinicopathologic data have for many years pointed to the frequent association between athetoid and choreiform hyperkinesias and lesions in the striatum (caudate nucleus and putamen) (1). A major obstacle to understanding the nature of these complex disorders has been the inability to reproduce any but evanescent manifestations of these symptoms by striatal lesions in lower animals (2).…”
mentioning
confidence: 99%
“…As long ago as 1911, Alzheimer had stated that there could " hardly be a remaining doubt " that in Huntington's chorea severe degenerative processes were regularly present in the cerebral cortex. Dunlap (1927), in his classical paper on the subject, remarked that in pure and well-developed instances of the disease there were constant lesions present in the cerebral cortex as well as in the corpus striatum, but he admitted that to date he had been unable to convince himself that there was any true loss of cortical cells. Minski and Guttmann (1938) remark that it does not seem possible to distinguish the dementia of Huntington's chorea from that in other types of dementing psychosis by any one specific feature such as a characteristic disturbance of thought.…”
Section: Dementia In Middle Agementioning
confidence: 99%