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J. Goldman, F. Chiu (1984)
Growth Kinetics, Cell Shape, and the Cytoskeleton of Primary Astrocyte CulturesJournal of Neurochemistry, 42
Wakabayashi Wakabayashi, Oyanagi Oyanagi, Makifuchi Makifuchi (1994)
Corticobasal degeneration: etiopathological significance of the cyto‐skeletal alterationsActa Neuropathol, 87
S. Kato, A. Hirano, T. Umahara, M. Kato, F. Herz, E. Ohama (1992)
Comparative immunohistochemical study on the expression of αB crystallin, ubiquitin and stress‐response protein 27 in ballooned neurons in various disordersNeuropathology and Applied Neurobiology, 18
M. Ruberg, F. Javoy‐Agid, E. Hirsch, B. Scatton, Rémy Lheureux, J. Hauw, C. Duyckaerts, F. Gray, A. Morel-Maroger, A. Rascol, M. Serdaru, Y. Agid (1985)
Dopaminergic and cholinergic lesions in progressive supranuclear palsyAnnals of Neurology, 18
S. Ohara, K. Kondo, H. Morita, K. Maruyama, S. Ikeda, N. Yanagisawa (1992)
Progressive supranuclear palsy‐like syndrome in two siblings of a consanguineous marriageNeurology, 42
J. Pascual, J. Berciano, Antonio González, B. Grijalba, J. Figols, Á. Pazos (1993)
Autoradiographic demonstration of loss of α 2-adrenoceptors in progressive supranuclear palsy: preliminary reportJournal of the Neurological Sciences, 114
Steele Steele, Richardson Richardson, Olszewski Olszewski (1964)
Progressive supranuclear palsyArch Neurol, 10
Hof Hof, Delacourte Delacourte, Bouras Bouras (1992)
Distribution of cortical neurofibrillary tangles in progressive supranuclear palsy: a quantitative analysis of six casesActa Neuropathol, 84
E. Masliah, L. Hansen, S. Quijada, R. DeTeresa, M. Alford, Joachim Kauss, R. Terry (1991)
Late onset dementia with argyrophilic grains and subcortical tangles or atypical progressive supranuclear palsy?Annals of Neurology, 29
T. Iwaki, A. Kume-Iwaki, R. Liem, J. Goldman (1989)
αB-crystallin is expressed in non-lenticular tissues and accumulates in Alexander's disease brainCell, 57
Jordan Grafman, Irene Litvan, Claudia Gomez, Thomas Chase (1990)
Frontal lobe function in progressive supranuclear palsy.Archives of neurology, 47 5
H. Sawa, I. Takeshita, M. Kuramitsu, H. Mannoji, T. Machi, M. Fukui, K. Kitamura (1986)
Neuronal and glial proteins in medulloblastomas. I. Immunohistochemical study.Anticancer research, 6 5
Horwtiz Horwtiz (1992)
α‐Crystallin can function as a molecular chaper‐oneProc Natl Acad Sci USA, 89
Mildred Hooper, F. Vogel (1976)
The limbic system in Alzheimer's disease. A neuropathologic investigation.The American journal of pathology, 85 1
Gibb Gibb, Luthert Luthert, Marsden Marsden (1989)
Corticobasal degenerationBruin, 112
(1936)
Die Picksche Krunklieit
H. Spatz (1937)
Über die Bedeutung der basalen RindeZeitschrift für die gesamte Neurologie und Psychiatrie, 158
Hiroshi Ishino, Saburo Otsuki (1976)
Frequency of Alzheimer's neurofibrillary tangles in the cerebral cortex in progressive supranuclear palsy (subcortical argyrophilic dystrophy)Journal of the Neurological Sciences, 28
J. Steele, Richardson Jc, J. Olszewski (1964)
PROGRESSIVE SUPRANUCLEAR PALSY. A HETEROGENEOUS DEGENERATION INVOLVING THE BRAIN STEM, BASAL GANGLIA AND CEREBELLUM WITH VERTICAL GAZE AND PSEUDOBULBAR PALSY, NUCHAL DYSTONIA AND DEMENTIA.Archives of neurology, 10
T. Iwaki, A. Iwaki, J. Tateishi, J. Goldman (1994)
Sense and antisense modification of glial alpha B-crystallin production results in alterations of stress fiber formation and thermoresistanceThe Journal of Cell Biology, 125
Pascual Pascual, Berciano Berciano, González González, Grijalba Grijalba, Figols Figols, Pazos Pazos (1993)
Autoradiographic demonstration of loss of α2–adrenoceptors in progressive supranuclear palsy: preliminary reportJ Neurol Sci, 144
J. Constantinidis, Jacques Richard, R. Tissot (1974)
Pick’s DiseaseEuropean Neurology, 11
(1974)
Picks Disease . Histological and clinical correlations
T. Iwaki, A. Kume-Iwaki, J. Goldman (1990)
Cellular distribution of alpha B-crystallin in non-lenticular tissues.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 38
T. Iwaki, T. Wisniewski, A. Iwaki, E. Corbin, N. Tomokane, J. Tateishi, J. Goldman (1992)
Accumulation of alpha B-crystallin in central nervous system glia and neurons in pathologic conditions.The American journal of pathology, 140 2
J. Lowe, D. Errington, G. Lennox, I. Pike, I. Spendlove, M. Landon, R. Mayer (1992)
Ballooned neurons in several neurodegenerative diseases and stroke contain αB crystallinNeuropathology and Applied Neurobiology, 18
Miyazono Miyazono, Iwaki Iwaki, Kitamoto Kitamoto, Shin Shin, Fukui Fukui, Tateishi Tateishi (1993)
Widespread distribution of tau in the astrocytic elements of glial tumorsActa Neuropathol, 86
Spatz Spatz (1937)
Über die Bedeutung der basalen Rinde, Aul' Grund von Beobachtungen bei Picksher Krankheit und bei gedeck‐ten HirnverletzungenZ. f. d. ges. Neurol Psychiatr, 158
P. Hof, J. Morrison, Kevin Cox (1990)
Quantitative analysis of a vulnerable subset of pyramidal neurons in Alzheimer's disease: I. Superior frontal and inferior temporal cortexJournal of Comparative Neurology, 301
R. Torack, J. Morris (1986)
Mesolimbocortical dementia. A clinicopathologic case study of a putative disorder.Archives of neurology, 43 10
J. Rebeiz, E. Kolodny, E. Richardson (1968)
Corticodentatonigral degeneration with neuronal achromasia.Archives of neurology, 18 1
Grünthal Grünthal (1936)
Die Picksche KrankheitHandbuch der Neurologie von Bumke-Foerster, II
Braak Braak, Jellinger Jellinger, Braak Braak, Bohl Bohl (1992)
Allocortical neuro‐fibrillary changes in progressive supranuclear palsyActa Neuropathol, 84
P. Whitehouse (1986)
The concept of subcortical and cortical dementia: Another lookAnnals of Neurology, 19
H. Takahashi, S. Takeda, F. Ikuta, Y. Homma (1987)
Progressive supranuclear palsy with limbic system involvement: report of a case with ultrastructural investigation of neurofibrillary tangles in various locations.Clinical neuropathology, 6 6
Sasaki Sasaki, Maruyama Maruyama, Toyoda Toyoda (1991)
A case of progressive supranuclear palsy with widespread senile plaquesJ Neurol, 238
H. Ksiȩżak-Reding, Karen Morgan, L. Mattiace, P. Davies, Wan‐Kyng Liu, S. Yen, K. Weidenheim, D. Dickson (1994)
Ultrastructure and biochemical composition of paired helical filaments in corticobasal degeneration.The American journal of pathology, 145 6
Gascon Gascon, Gilles Gilles (1973)
Limbic dementiaJ Neurol Neurosurg Psych, 36
J. Hauw, M. Verny, P. Delaère, P. Cervera, Y. He, C. Duyckaerts (1990)
Constant neurofibrillary changes in the neocortex in progressive supranuclear palsy. Basic differences with Alzheimer's disease and agingNeuroscience Letters, 119
S. Kish, L. Chang, L. Mirchandani, K. Shannak, O. Hornykiewicz (1985)
Progressive supranuclear palsy: Relationship between extrapyramidal disturbances, dementia, and brain neurotransmitter markersAnnals of Neurology, 18
J. Horwitz (1992)
Alpha-crystallin can function as a molecular chaperone.Proceedings of the National Academy of Sciences of the United States of America, 89 21
J. Jules
a-Crystallin can function as a molecular chaperone ( aggregation / heat shock / renaturation / eye lens proteins )
(1986)
Corticobasal preliminary report
Mori Mori, Nishimura Nishimura, Namba Namba, Oda Oda (1994)
Corticobasal degeneration: a disease with widespread appearance of abnormal tau and neurofibrillary tangles. and its relation to progressive supranuclear palsyActa Neuropathol, 88
K. Jellinger (1988)
The pedunculopontine nucleus in Parkinson's disease, progressive supranuclear palsy and Alzheimer's disease.Journal of Neurology, Neurosurgery & Psychiatry, 51
B. Dubois, B. Pillon, Françoise Legault, Y. Agid, F. Lhermitte (1988)
Slowing of cognitive processing in progressive supranuclear palsy. A comparison with Parkinson's disease.Archives of neurology, 45 11
(1994)
Corticodentatoni- skeletal alterations
F. Tagliavini, G. Pilleri, Constantin Bouras, J. Constantinidis (1984)
The basal nucleus of Meynert in patients with progressive supranuclear palsyNeuroscience Letters, 44
S. Huber, G. Paulson (1985)
The concept of subcortical dementia.The American journal of psychiatry, 142 11
Progressive supranuclear palsy is neuropathologically characterized by neuronal degeneration of the basal ganglia, brain stem, and cerebellum. In addition, cortical neuronal degeneration associated with neurofibrillary tangles formation has been identified over wide areas of the brain in patients with progressive supranuclear palsy. We studied the distribution of αB‐crystallin‐positive degenerating neurons in cases with progressive supranuclear palsy, and compared them with those in Pick's disease, Alzheimer's disease, senile dementia of Alzheimer type, and normal aged individuals. A large number of αB‐crystallin‐positive neurons was found in the cerebral cortices of four out of nine patients with progressive supranuclear palsy. In particular, αB‐crystallin‐positive ballooned neurons were frequently observed in deep cortical pyramidal cell layers of the limbic and paralimbic systems in these diseases. The involvement of the limbic and paralimbic systems may thus contribute to personality changes as well as to memory and cognitive impairment in some patients with progressive supranuclear palsy.
Neuropathology & Applied Neurobiology – Wiley
Published: Jun 1, 1995
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