Frontotemporal dementia: A review

Journal of the International Neuropsychological Society

Volumn 8, Issue 4, 2002, Pages 566-583

  Grossman, Murray ^a  

^a HOSPITAL OF THE UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Frontotemporal dementia; Neuropsychiatric impairment; Progressive aphasia; Semantic dementia

Indexed keywords

ALZHEIMER DISEASE; APHASIA; BEHAVIOR DISORDER; CLINICAL FEATURE; CONTROLLED STUDY; DIAGNOSTIC IMAGING; DIFFERENTIAL DIAGNOSIS; FRONTOTEMPORAL DEMENTIA; HEALTH PRACTITIONER; HUMAN; NEUROPATHOLOGY; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; REVIEW; SINGLE PHOTON EMISSION COMPUTER TOMOGRAPHY;

AGED; APHASIA; COGNITION DISORDERS; DEMENTIA; FRONTAL LOBE; HUMANS; NEUROPSYCHOLOGICAL TESTS; SEMANTICS; SEVERITY OF ILLNESS INDEX; TEMPORAL LOBE;

EID: 0036265512     PISSN: 13556177     EISSN: None     Source Type: Journal    
DOI: 10.1017/S1355617702814357     Document Type: Review

References (178)

1. Arterial spin labeling perfusion MRI in frontotemporal dementia and Alzheimer's disease: Correlation with language functions
2. Uber die umschriebene Gehirnatrophie des spateren Alters
3. Uber eigenartige Krankheitsfalle der spateren Alters
4. Molecular genetic characterization of frontotemporal dementia on chromosome 3
5. Cognition, language and behavior in Motor Neurone disease: Evidence of frontotemporal dysfunction
6. Selective impairment of verb processing associated with pathological changes in Brodmann areas 44 and 45 in the motor neurone disease-dementia-aphasia syndrome
7. Progressive language impairment without dementia: A case with isolated category-specific semantic impairment
8. Executive function in early Alzheimer disease
9. Pick's disease in old age
10. Chromosome 17 and hereditary dementia: Linkage studies in three non-Alzheimer families and kindreds with late-onset FAD
11. Neuropsychological patterns in right versus left frontotemporal dementia
12. Which neuropsychiatric and behavioural features distinguish frontal and temporal variants of frontotemporal dementia from Alzheimer's disease?
13. Familial non-specific dementia maps to chromosome 3
14. Frontal lobe degeneration of the non-Alzheimer type: I. Neuropathology
15. The Lund longitudinal dementia study. A 25 year perspective on neuropathology, differential diagnosis, and treatment
16. Object and action naming in Alzheimer's disease and fronto-temporal dementia
17. Living/nonliving dissociation in a case of semantic dementia: SPECT activation study
18. Asymmetric cortical degeneration syndromes: A proposed clinical classification
19. Rapidly progressive aphasic dementia and motor neuron disease
20. Slowly progressive aphasia without dementia: Studies with positron emission tomography
21. Progressive amusia and aprosody
22. Pick dementia. Anatomoclinical correlations and pathophysiological considerations
23. Pick's disease: Histological and clinical correlations
24. Sentence comprehension in frontotemporal dementia subgroups: Evidence from neuroimaging
25. Kluver-Bucy syndrome in Pick disease: Clinical and pathological correlations
26. The Neuropsychiatric Inventory: Comprehensive assessment of psychopathology in dementia
27. Evaluating the clinical diagnosis of frontotemporal degeneration: A re-examination of Neary et al., 1998
28. Slowly progressive visual agnosia or apraxia without dementia
29. Cerebral blood flow in progressive aphasia without dementia
30. Provisional clinical and neuroradiological criteria for the diagnosis of Pick's disease
31. The temporal variant of frontotemporal dementia
32. Neuropsychological tests as discriminators between dementia of Alzheimer type and frontotemporal dementia
33. Neuropsychological findings in frontal lobe dementia
34. Progressive prosopagnosia associated with selective right temporal lobe atrophy
35. Dementia of frontal lobe type and motor neuron disease. A golgi study of the frontal cortex
36. "Mini Mental State." A practical method for grading the cognitive state of patients for the clinician
37. Frontotemporal dementia and Parkinsonism linked to chromosome 17: A consensus conference
38. Dementia of the frontal lobe type: Neuropsychological and [99Tc]-HM-PAO SPECT features
39. Evidence for scripts in Semantic Dementia: Implications for theories of semantic memory
40. Visual processing in frontotemporal dementia and Alzheimer's disease
41. Differing patterns of temporal atrophy in Alzheimer's disease and semantic dementia
42. Atypical and typical presentations of Alzheimer's disease: A clinical, neuropsychological, neuroimaging, and pathological study of 13 cases
43. Betrachtungen uber Art und Ausbreitung des krankhaften Prozesses in einem Fall von Pickscher Atrophie des Stirnhirns
44. Dementia lacking distinctive histopathology: Clinicopathological evaluation of 32 cases
45. On the relationship between senile cerebral atrophy and aphasia
46. On the symptomatology of left-sided temporal lobe atrophy
47. Progressive aphasia in a patient with Pick's disease
48. Differentiating the roles of the hippocampal complex and the neocortex in long-term memory storage: Evidence from the study of semantic dementia and Alzheimer's disease
49. Determining the impact of autobiographical experience on "meaning": New insights from investigating sports-related vocabulary and knowledge in two cases of Semantic Dementia
50. Relearning and subsequent forgetting of semantic category exemplars in a case of Semantic Dementia
51. A reverse temporal gradient for public events in a single case of semantic dementia
52. Progressive aphasia: A precursor of global dementia?
53. Dementia of frontal type and the focal lobar atrophies
54. Frontotemporal dementia: Use of consensus criteria and prevalence of psychiatric features
55. Can frontotemporal dementia and Alzheimer's disease be differentiated using a brief battery of tasks?
56. Early diagnosis of the frontal variant of frontotemporal dementia: How sensitive are standard neuroimaging and neuropsychologic tests?
57. Hereditary Pick's disease: Second re-examination of a large family and discussion of other hereditary cases, with particular reference to electroencephalography and computerized tomography
58. Language comprehension difficulty in Alzheimer's disease, vascular dementia, and fronto-temporal degeneration
59. Progressive non-fluent aphasia: Language, cognitive and PET measures contrasted with probable Alzheimer's disease
60. Language comprehension and regional cerebral defects in frontotemporal degeneration and Alzheimer's disease
61. Sentence processing in frontotemporal degeneration
62. Frontal lobe degeneration of the non-Alzheimer type. II. Clinical picture and differential diagnosis
63. Clinical picture of frontal lobe degeneration of non-Alzheimer type
64. Frontal lobe degeneration of the non-Alzheimer type
65. Differential diagnosis of presenile dementia on clinical grounds
66. Diseases presenting as dementia
67. A reversal of the temporal gradient for famous person knowledge in semantic dementia: Implications for the neural organization of long-term memory
68. Nonfluent progressive aphasia and semantic dementia: A comparative neuropsychological study
69. Semantic dementia: Progressive fluent aphasia with temporal lobe atrophy
70. The differentiation of semantic dementia and frontal lobe dementia (temporal and frontal variants of frontotemporal dementia) from early Alzheimer's disease: A comparative neuropsychological study
71. The dissolution of language in Pick's disease with neurofibrillary tangles: A case study
72. Tau-based neurofibrillary lesions
73. Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17
74. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
75. Motor-neuron disease-inclusion dementia
76. Clinical-physiologic correlates of Alzheimer's disease and frontal lobe dementia
77. Psychometric characteristics in patients with frontal lobe degeneration of non-Alzheimer type
78. Clinical and pathological evidence for a frontal variant of Alzheimer disease
79. Profiles of language impairment in Primary Progressive Aphasia
80. Primary progressive non-fluent aphasia: A case study
81. Slowly progressive aphasia: Three cases with language, memory, CT, and PET data
82. Frontotemporal dementia, Pick's disease, and corticobasal degeneration
83. The pathology and nosology of primary progressive aphasia
84. Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions
85. Progressive aphasia without dementia: Two cases with focal spongiform degeneration
86. Incorrect diagnosis of Alzheimer's disease: A clinicopathological study
87. The spectrum of imaging and neuropsychological findings in Pick's disease
88. Dementia lacking distinctive histologic features: A common non-Alzheimer degenerative dementia
89. Lexical and semantic binding effects in short-term memory: Evidence from Semantic Dementia
90. No right to speak? The relationship between object naming and semantic impairment: Neuropsychological evidence and a computational model
91. Alzheimer disease and frontotemporal dementias: Behavioral distinctions
92. Human autonomy and the frontal lobes. Part I: Imitation and utilization behavior: A neuropsychological study of 75 patients
93. Cognitive, neuroimaging, and pathologic studies in a patient with Pick's disease
94. Cognitive and behavioral differentiation of frontal lobe degeneration of the non-Alzheimer type and Alzheimer's disease
95. Primary progressive aphasia with focal neuronal achromasia
96. What are the obstacles for an accurate clinical diagnosis of Pick's disease? A clinicopathologic study
97. Symptoms of depression and psychosis in Alzheimer's disease and frontotemporal dementia
98. Dissociation of social cognition and executive function in frontal variant frontotemporal dementia
99. Occurrence of Pick's disease in early adult years
100. An early description of slowly progressive aphasia
101. Pick's disease with atrophy of the temporal lobes
102. Dementia of frontal lobe type: Neuropathology and immunohistochemistry
103. A brief cognitive test battery to differentiate Alzheimer's disease and frontotemporal dementia
104. Repeating without semantics: Surface dysphasia?
105. Clinical diagnosis of Alzheimer's disease: Report on the NINCDS-ADRDA work group under the auspices of the Department of Health and Human Services Task Force on Alzheimer's disease
106. Clinical and pathological diagnosis of frontotemporal dementia: Report of a work group on frontotemporal dementia and Pick's disease
107. Self-injurious behavior in frontotemporal dementia
108. Frontotemporal dementia versus Alzheimer's disease: Differential cognitive features
109. Pick's disease vs. Alzheimer's disease: A comparison of clinical characteristics
110. Slowly progressive aphasia without generalized dementia
111. Clinical and imaging features of right focal frontal lobe degenerations
112. Frontal lobe degeneration: Clinical, neuropsychological, and SPECT characteristics
113. Aggressive, socially disruptive and anti-social behaviour associated with fronto-temporal dementia
114. Dietary changes, compulsions, and sexual behavior in frontotemporal degeneration
115. A study of the Lund-Manchester research criteria for frontotemporal dementia: Clinical and single photon emission CT correlations
116. Disrupted temporal lobe connections in semantic dementia
117. Semantic Dementia: Relevance to connectionist models of long-term memory
118. Novel applications of social-personality measures to the study of dementia
119. Frontotemporal degeneration, Pick's disease, and corticobasal degeneration
120. Fronto-temporal dementia: Nosology, neuropsychology, and neuropathology
121. Frontotemporal lobar degeneration: A consensus on clinical diagnostic criteria
122. Frontal lobe dementia and motor neuron disease
123. Dementia of frontal lobe type
124. Single photon emission tomographic imaging of the brain using -super(99m)Tc-HM-PAO in the investigation of dementia
125. Reading in dementia
126. New ubiquitin-positive intraneuronal inclusions in the extra-motor cortices in patients with amyotrophic lateral sclerosis
127. Anatomische Beitrage zur Lehre von Picksnen umschriebenen Grosshirnrinden-Atrophie ("Picksche Krankheit")
128. Self-neglect and frontal lobe dysfunction
129. Comparison of neuropsychological functioning in Alzheimer's disease and frontotemporal dementia
130. Progressive aphasia without dementia-A clinical and cognitive neuropsychological analysis
131. Memory impairment differs in frontotemporal dementia and Alzheimer's disease
132. Verbal fluency in dementia of frontal lobe type and dementia of Alzheimer type
133. The impact of semantic memory loss on phonologic representations
134. Deterioration of word meaning: Implications for reading
135. Hemispheric dominance for emotions, empathy, and social behaviour: Evidence from right and left-handers with frontotemporal dementia
136. Über die Beziehungen der senilen Hirnatrophie zue Aphasie
137. Zur Symptomalogie der linksseitigen Schafenlappenatrophie
138. Slowly progressive aphasia in three patients
139. Alzheimer's disease presenting as slowly progressive aphasia
140. Tau is a candidate gene for chromosome 17 Frontotemporal dementia
141. Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia
142. Clinical diagnosis of Frontotemporal dementia (FTD)
143. Specific cognitive deficits in mild frontal variant frontotemporal dementia
144. Verb comprehension in frontotemporal degeneration: The role of grammatical, semantic and executive components
145. Frontal lobe degeneration of non-Alzheimer type. III. Regional cerebral blood flow
146. High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands
147. Die partielle grosshirnatrophie
148. Differential diagnosis of frontotemporal dementia: Pick's disease
149. Semantic Dementia with ubiquitin-positive tau-negative inclusion bodies
150. Surface dyslexia in an Italian patient with semantic dementia
151. A case of progressive aphasia without dementia: "Temporal" Pick's disease?
152. Pathologic findings in a case of primary progressive aphasia
153. A case of primary progressive aphasia: A 14-year follow-up study with neuropathological findings
154. Semantic dysfunction in frontotemporal lobar degeneration
155. Semantic dementia: A form of circumscribed cerebral atrophy
156. Semantic dementia: Autobiographical contribution to preservation of meaning
157. Semantic-episodic memory interactions in semantic dementia: Implications for retrograde memory function
158. Progressive language dysfunction and lobar atrophy
159. Frontotemporal lobar degeneration: Fronto-temporal dementia, progressive aphasia, semantic dementia
160. Progressive language disorder due to lobar atrophy
161. Mutation in the tau gene in familial multiple system tauopathy with presenile dementia
162. Specificity of changes in cerebral blood flow in patients with frontal lobe dementia
163. Clinical and neuropathological criteria for frontotemporal dementia
164. Pick's disease
165. Clinical, neuroimaging, and pathologic features of progressive non-fluent aphasia
166. The gradual deterioration of syntax and semantics in a patient with progressive aphasia
167. Progressive loss of speech output and orofacial dyspraxia associated with frontal lobe hypometabolism
168. Heterogeneity in progressive aphasia due to focal cortical atrophy: A clinical and PET scan study
169. Progressive degeneration of the right temporal lobe studied with positron emission tomography
170. Evaluation of the NINCDS-ADRDA criteria in the differentiation of Alzheimer's disease and frontotemporal dementia
171. The selective impairment of semantic memory
172. Surface dyslexia in nonfluent progressive aphasia
173. Presenile dementia presenting as aphasia
174. Pick's disease: A clinical, computed tomographic, and histologic study with golgi impregnation
175. Primary progressive aphasia: Longitudinal course, neuropsychological profile, and language features
176. Hippocampal and neocortical ubiquitin-immunoreactive inclusions in amyotrophic lateral sclerosis
177. Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22
178. Loss of brain tau defines novel sporadic and familial tauopathies with frontotemporal dementia