Neuropathology of Pick's disease

Neurology

Volumn 56, Issue 11 SUPPL. 4, 2001, Pages

  Dickson, D W ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN ATROPHY; DISEASE CLASSIFICATION; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; IMMUNOCHEMISTRY; NEUROPATHOLOGY; PICK PRESENILE DEMENTIA; PRIORITY JOURNAL; REVIEW;

EID: 0034975898     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.56.suppl_4.s16     Document Type: Review

References (81)

1. Pick dementia. Anatomoclinical correlations and pathophysiological considerations
2. Clinical and pathological characteristics of primary progressive aphasia and frontal dementia
3. Corticobasal degeneration
4. Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference
5. Dementia lacking distinctive histopathology: Clinicopathological evaluation of 32 cases
6. The neuropathologic diagnostic criteria of frontal lobe dementia revisited. A study of ten consecutive cases
7. Dementia lacking distinctive histologic features: A common non-Alzheimer degenerative dementia
8. Fronto-temporal dementia: Nosology, neuropsychology, and neuropathology
9. Striatopallidonigral degeneration in Pick's disease: A clinicopathological study of 41 cases
10. Lobar atrophy without Pick bodies
11. The peculiar cells of Pick's disease: Their pathogenesis and distribution in disease
12. Immunocytochemical and ultrastructural studies of Pick's disease
13. Pick bodies in the locus ceruleus
14. Presence of two different fibril subtypes in the Pick body: An immunoelectron microscopic study
15. Electron microscopic structure of the "inclusion bodies" in Pick's disease
16. Ballooned neurons in select neurodegenerative diseases contain phosphorylated neurofilament epitopes
17. Cortical degeneration with swollen chromatolytic neurons: Its relationship to Pick's disease
18. Comparative immunohistochemical study on the expression of alpha B crystallin ubiquitin and stress-response protein 27 in ballooned neurons in various disorders
19. Ballooned neurons in several neurodegenerative diseases and stroke contain alpha B crystallin
20. Topography of Pick body distribution in Pick's disease: A contribution to understanding the relationship between Pick's and Alzheimer's diseases
21. Immunoelectron microscopy of Alzheimer and Pick brain tissue labeled with the monoclonal antibody Alz-50
22. Classic and generalized variants of Pick's disease: A clinicopathological ultrastructural and immunocytochemical comparative study
23. An ultrastructural study of Pick bodies
24. Pick's disease: A clinical and ultrastructural study
25. Monoclonal antibodies to Alzheimer neurofibrillary tangles (ANT): Demonstration of a common antigenic determinant between ANT and neurofibrillary degeneration in progressive supranuclear palsy
26. Filaments of Pick's bodies contain altered cytoskeletal elements
27. Alzheimer dementia and Pick's disease: Neurofibrillary tangles and Pick bodies are associated with identical phosphorylated neurofilament epitopes
28. Pick's disease: An immunocytochemical study of neuronal changes. Monoclonal antibodies show that Pick bodies share antigenic determinants with neurofibrillary tangles and neurofilaments
29. Cytoskeletal abnormalities in neuropathology
30. Sharing of specific antigens by degenerating neurons in Pick's disease and Alzheimer's disease
31. Alz-50, ubiquitin and tau immunoreactivity of neurofibrillary tangles Pick bodies and Lewy bodies
32. Filamentous aggregates in Pick's disease, progressive supranuclear palsy, and Alzheimer's disease share antigenic determinants with microtubule-associated protein tau
33. Pick's disease: Hyperphosphorylated tau protein segregates to the somatoaxonal compartment
34. Extracellular or ghost Pick bodies and their lack of tau immunoreactivity: A histological immunohistochemical and electron microscopic study
35. Ubiquitin the cytoskeleton and neurodegenerative disease
36. Ubiquitin is a common factor in intermediate filament inclusion bodies of diverse type in man including those of Parkinson's disease, Pick's disease, and Alzheimer's disease as well as Rosenthal fibres in cerebellar astrocytomas cytoplasmic bodies in muscle and Mallory bodies in alcoholic liver disease
37. A high ratio of chromogranin A to synaptin/synaptophysin is a common feature of brains in Alzheimer and Pick disease
38. Expression of chromogranin A in lesions in the central nervous system from patients with neurological diseases
39. Alpha-synuclein in Lewy bodies
40. Evidence for oxidative stress in Pick disease and corticobasal degeneration
41. Identification of advanced glycation end products of the Maillard reaction in Pick's disease
42. 4-Hydroxy-2-nonenal pyrrole adducts in human neurodegenerative disease
43. Neocortical morphometry and cholinergic neurochemistry in Pick's disease
44. Quantitative immunohistochemistry of synaptophysin in human neocortex: An alternative method to estimate density of presynaptic terminals in paraffin sections
45. Neuropathological changes of the temporal pole in Alzheimer's disease and Pick's disease
46. Image analysis of neuropil threads in Alzheimer's, Pick's, diffuse Lewy body disease and in progressive supranuclear palsy
47. Severe panencephalic Pick's disease with Alzheimer's disease-like neuropil threads and synaptophysin immunoreactivity
48. Pick's disease immunohistochemistry: New alterations and Alzheimer's disease comparisons
49. Topography of Pick inclusion bodies in hippocampi of demented patients. A quantitative study
50. Neuropathological study on the nucleus basalis of Meynert in Pick's disease
51. Basal nucleus of Meynert: A neuropathological study in Alzheimer's disease, simple senile dementia, Pick's disease, and Huntington's chorea
52. Pick's disease (lobar sclerosis): Depletion of neurons in the nucleus basalis of Meynert
53. A post-mortem comparison of the cortical cholinergic system in Alzheimer's disease and Pick's disease
54. Lack of cholinergic deficit in the neocortex in Pick's disease
55. Selective loss of nigral neurons in Pick's disease: A morphometric study
56. Involvement of the locus coeruleus in Pick's disease with or without Pick body formation
57. Coexistence of Pick bodies and atypical Lewy bodies in the locus ceruleus neurons of Pick's disease
58. Pontine cytoskeletal pathology in the differential diagnosis of non-Alzheimer dementias
59. Neurodegenerative diseases with cytoskeletal pathology: A biochemical classification
60. Morphological overlap between corticobasal degeneration and Pick's disease: A clinicopathological report
61. Astrocytic straight tubules in the brain of a patient with Pick's disease
62. Cytoskeletal pathology in non-Alzheimer degenerative dementia: New lesions in diffuse Lewy body disease, Pick's disease, and corticobasal degeneration
63. Neuropathologic overlap of progressive supranuclear palsy, Pick's disease and corticobasal degeneration
64. Microglial reaction in Pick's disease
65. Neuronal expression of class II major histocompatibility complex (HLA-DR) in 2 cases of Pick disease
66. Role of complement in the aetiology of Pick's disease?
67. Expression of the complement membrane attack complex and its inhibitors in Pick disease brain
68. Isolation of the insoluble straight fibrils of Pick's disease
69. Mechanical instability of Pick bodies and their isolation in an intact form using urea solution
70. Alzheimer-related neuronal protein A-68: Specificity and distribution
71. Hyperphosphorylated tau proteins differentiate corticobasal degeneration and Pick's disease
72. Specific pathological tau protein variants characterize Pick's disease
73. Different distribution of phosphorylated tau protein isoforms in Alzheimer's and Pick's diseases
74. Widespread cytoskeletal pathology characterizes corticobasal degeneration
75. Parietal Pick's disease mimicking cortical-basal ganglionic degeneration
76. The pathology and nosology of primary progressive aphasia
77. The new neuropathology of degenerative frontotemporal dementias
78. Dementia of frontal lobe type: Neuropathology and immunohistochemistry
79. New ubiquitin-positive intraneuronal inclusions in the extra-motor cortices in patients with amyotrophic lateral sclerosis
80. Hippocampal and neocortical ubiquitin-immunoreactive inclusions in amyotrophic lateral sclerosis with dementia
81. Primary progressive aphasia with focal neuronal achromasia