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1 ith those areas known to be most affected in semantic dementia.
2 ormed markedly better than the patients with semantic dementia.
3 face and name knowledge in 15 patients with semantic dementia.
4 vanced interpretations of the impairments in semantic dementia.
5 pposed to the 'storage' deficits observed in semantic dementia.
6 ts of picture-naming data from patients with semantic dementia.
7 that is sensitive to semantic impairment in semantic dementia.
8 of a more severe generic semantic deficit in semantic dementia.
9 visual deficits as compared to patients with semantic dementia.
10 its, but sparing of phonology and fluency in semantic dementia.
11 the widely accepted diagnostic criteria for semantic dementia.
12 ad criteria, excluding only those with clear semantic dementia.
13 tices and nucleus accumbens in patients with semantic dementia.
14 ), progressive non-fluent aphasia (PNFA) and semantic dementia.
15 t mortem cases meeting clinical criteria for semantic dementia.
16 al levels: progressive nonfluent aphasia and semantic dementia.
17 h progressive non-fluent aphasia; eight with semantic dementia].
18 on this test of a group of 12 patients with semantic dementia (10 male, mean age: 64.4 years) correl
19 2% bvFTD/motor neuron disease cases), 2 with semantic dementia (5.9% of patients with semantic dement
20 t frontotemporal dementia (71% of cases) and semantic dementia (65% of cases) and in association with
21 ic cases) and heightened responsiveness with semantic dementia (73% of symptomatic cases) and Alzheim
22 er of central conceptual knowledge arises in semantic dementia, a degenerative condition associated w
26 expert musicians with clinical diagnoses of semantic dementia and Alzheimer's disease, in comparison
29 l eating behavior in patients with bvFTD and semantic dementia and are likely responsible for the dif
30 heimer's disease, the focal lobar atrophies (semantic dementia and dementia of frontal type) and thre
31 t the performance of three patients-two with semantic dementia and focal temporal lobe atrophy and th
32 teria for behavioural variant FTD (bvFTD) or semantic dementia and had characteristic brain atrophy.
33 asting doubt over the conclusions drawn from semantic dementia and linked basic neuroscience studies.
34 h clinical diagnoses of Alzheimer's disease, semantic dementia and non-fluent primary progressive aph
35 osia is one of the clinical presentations of semantic dementia and not a separate clinical entity.
37 h those observed in a group of patients with semantic dementia and predominant left-sided temporal lo
38 ic prominence, particularly for diagnosis in semantic dementia and prognosis in behavioural syndromes
39 ible for deteriorating semantic knowledge in semantic dementia and separate from 'classic' language a
41 psychological studies of surface dyslexia in semantic dementia and the connectionist triangle model o
42 s an examination of the relationship between semantic dementia and the focal clinical syndrome of pro
43 totemporal dementia with motoneuron disease, semantic dementia and, with one exception, progressive n
44 tients (five with svPPA and two with 'right' semantic dementia) and 12 healthy controls underwent pos
45 ith semantic dementia (5.9% of patients with semantic dementia), and none with progressive nonfluent
46 tients with dementia (19 with bvFTD, 15 with semantic dementia, and 15 with Alzheimer disease) were r
47 f primary progressive aphasia, also known as semantic dementia, and Alzheimer's disease have deficits
48 d in both progressive non-fluent aphasia and semantic dementia, and deficits of semantic processing a
49 clear palsy set), anterior temporal lobes in semantic dementia, and hippocampus and posterior cingula
50 ding of the anatomical changes that occur in semantic dementia, and may further help to explain the d
52 h the volume of right temporal structures in semantic dementia, and with subcallosal gyrus volume in
53 rment of semantic knowledge in patients with semantic dementia appears to influence performance in a
54 ant primary progressive aphasia (also called semantic dementia) are two clinical variants of frontote
55 s suggested by observations on patients with semantic dementia, as well as posterior regions describe
56 a striking literary depiction of collective semantic dementia before the syndrome was recognized in
57 hat differed between patients with bvFTD and semantic dementia but included the cingulate cortices, t
60 ecent findings indicate that the syndrome of semantic dementia can inform us about the organisation o
61 a visual decision task in four patients with semantic dementia compared with six age-matched normal c
62 longitudinal bundle, where abnormalities in semantic dementia did not extend caudal to the atrophic/
63 [(18)F]AV-1451, the pathological regions in semantic dementia do not normally contain significant le
64 [(18)F]AV-1451 binding potential, separated semantic dementia from controls with 86% sensitivity and
66 ilateral anterior temporal lobe damage (e.g. semantic dementia), functional neuroimaging and repetiti
67 ative threshold, tensor abnormalities in the semantic dementia group mapped onto the tractographies f
74 performed on a wider cohort of patients with semantic dementia, in which the patients with more exten
77 d the hypothesis that concept degradation in semantic dementia involves a combination of these pan-mo
85 the Alzheimer disease (mean, 710 calories), semantic dementia (mean, 573 calories), and control grou
87 ral variant FTD (n = 26), language variants (semantic dementia, n = 9; and progressive nonfluent apha
88 havioral variant frontotemporal dementia and semantic dementia, often respond to treatment with selec
89 dial temporal lobe lesions and patients with semantic dementia on nine tests of semantic knowledge an
90 al dementia, progressive non-fluent aphasia, semantic dementia or mixture of these syndromes for muta
91 longitudinal fasciculus were tracked in five semantic dementia patients and eight healthy controls.
93 ', strategies that resonate with attempts by semantic dementia patients to cope with their disease.
95 erall profile masked individual differences: semantic dementia patients with predominant left tempora
96 Three groups of 10 subjects were studied: semantic dementia patients, Alzheimer's disease patients
97 the tests of new learning, the patients with semantic dementia performed markedly better than the amn
98 r each FTD subtype (behavioural variant FTD, semantic dementia, progressive non-fluent aphasia, and F
99 drome that includes frontotemporal dementia, semantic dementia, progressive nonfluent aphasia and pro
103 wo groups suffering from different diseases: semantic dementia (SD) and herpes simplex virus encephal
105 with frontotemporal dementia (FTD), 19 with semantic dementia (SD) and six with progressive non-flue
108 diverse cortical regions in semantic memory: semantic dementia (SD) is characterized by atrophy of th
109 ed patients with Alzheimer's disease (AD) or semantic dementia (SD) on a visual oddity judgment task
110 ral atrophy of the anterior temporal lobe in semantic dementia (SD) produces a gradual degradation of
111 herpes simplex virus encephalitis (HSVE) and semantic dementia (SD) typically affect anterior tempora
114 uent aphasia (PNFA) (or a mixed aphasia) and semantic dementia (SD); and to compare the age of onset,
115 onfluent progressive aphasia (NFPA; n = 11), semantic dementia (SD; n = 10), and a third variant term
116 18 progressive nonfluent aphasia [PNFA], 16 semantic dementia [SD]), 22 progressive supranuclear pal
120 rment found across different patient groups (semantic dementia, temporal lobe epilepsy, glioma and st
121 The cortical anatomy of 6 patients with semantic dementia (the temporal lobe variant of frontote
122 convincingly demonstrated that patients with semantic dementia (the temporal variant of frontotempora
127 est to evaluate the ability of patients with semantic dementia to use recollection-based memory proce
128 e left language-related cerebral pathways in semantic dementia using diffusion tensor imaging-based t
131 To explore this phenomenon in nine cases of semantic dementia, we designed a set of semantic tests r
133 uced fractional anisotropy for patients with semantic dementia were spatially concordant with each ot
134 frontotemporal dementia alone, one had mixed semantic dementia with frontal features and three had pr
135 or temporal lobe structures were affected in semantic dementia, with the entorhinal cortex, amygdala,
136 ntext of their implications for the place of semantic dementia within the classification of progressi
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