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1
Longitudinal white matter change in frontotemporal dementia subtypes and sporadic late onset Alzheimer's disease.
Elahi, Fanny M; Marx, Gabe; Cobigo, Yann. - : eScholarship, University of California, 2017
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2
Data-driven classification of patients with primary progressive aphasia
In: Hoffman, P; Sajjadi, SA; Patterson, K; & Nestor, PJ. (2017). Data-driven classification of patients with primary progressive aphasia. BRAIN AND LANGUAGE, 174, 86 - 93. doi:10.1016/j.bandl.2017.08.001. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/5m4842c0 (2017)
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3
Longitudinal white matter change in frontotemporal dementia subtypes and sporadic late onset Alzheimer's disease.
Elahi, Fanny M; Marx, Gabe; Cobigo, Yann. - : eScholarship, University of California, 2017
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4
Data-driven classification of patients with primary progressive aphasia.
Nestor, Peter J; Sajjadi, Seyed Ahmad; Patterson, Karalyn. - : eScholarship, University of California, 2017
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5
Data-driven regions of interest for longitudinal change in three variants of frontotemporal lobar degeneration
In: Binney, RJ; Pankov, A; Marx, G; He, X; McKenna, F; Staffaroni, AM; et al.(2017). Data-driven regions of interest for longitudinal change in three variants of frontotemporal lobar degeneration. BRAIN AND BEHAVIOR, 7(4), e00675. doi:10.1002/brb3.675. UCSF: Retrieved from: http://www.escholarship.org/uc/item/1xd9f3hr (2017)
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6
A neural network underlying intentional emotional facial expression in neurodegenerative disease.
Gola, Kelly A; Shany-Ur, Tal; Pressman, Peter. - : eScholarship, University of California, 2017
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7
A neural network underlying intentional emotional facial expression in neurodegenerative disease.
Gola, Kelly A; Shany-Ur, Tal; Pressman, Peter. - : eScholarship, University of California, 2017
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8
A neural network underlying intentional emotional facial expression in neurodegenerative disease
In: Gola, KA; Shany-Ur, T; Pressman, P; Sulman, I; Galeana, E; Paulsen, H; et al.(2017). A neural network underlying intentional emotional facial expression in neurodegenerative disease. NEUROIMAGE-CLINICAL, 14, 672 - 678. doi:10.1016/j.nicl.2017.01.016. UCSF: Retrieved from: http://www.escholarship.org/uc/item/9kp6g3dm (2017)
Abstract: Intentional facial expression of emotion is critical to healthy social interactions. Patients with neurodegenerative disease, particularly those with right temporal or prefrontal atrophy, show dramatic socioemotional impairment. This was an exploratory study examining the neural and behavioral correlates of intentional facial expression of emotion in neurodegenerative disease patients and healthy controls. One hundred and thirty three participants (45 Alzheimer's disease, 16 behavioral variant frontotemporal dementia, 8 non-fluent primary progressive aphasia, 10 progressive supranuclear palsy, 11 right-temporal frontotemporal dementia, 9 semantic variant primary progressive aphasia patients and 34 healthy controls) were video recorded while imitating static images of emotional faces and producing emotional expressions based on verbal command; the accuracy of their expression was rated by blinded raters. Participants also underwent face-to-face socioemotional testing and informants described participants' typical socioemotional behavior. Patients' performance on emotion expression tasks was correlated with gray matter volume using voxel-based morphometry (VBM) across the entire sample. We found that intentional emotional imitation scores were related to fundamental socioemotional deficits; patients with known socioemotional deficits performed worse than controls on intentional emotion imitation; and intentional emotional expression predicted caregiver ratings of empathy and interpersonal warmth. Whole brain VBMs revealed a rightward cortical atrophy pattern homologous to the left lateralized speech production network was associated with intentional emotional imitation deficits. Results point to a possible neural mechanisms underlying complex socioemotional communication deficits in neurodegenerative disease patients.
Keyword: Emotion; Empathy; Facial expression; Frontotemporal dementia; Social functioning
URL: http://www.escholarship.org/uc/item/9kp6g3dm
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9
Data-driven regions of interest for longitudinal change in three variants of frontotemporal lobar degeneration.
In: Brain and behavior, vol 7, iss 4 (2017)
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10
Observing conversational laughter in frontotemporal dementia.
In: Journal of neurology, neurosurgery, and psychiatry, vol 88, iss 5 (2017)
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11
Emotion detection deficits and changes in personality traits linked to loss of white matter integrity in primary progressive aphasia.
Multani, Namita; Galantucci, Sebastiano; Wilson, Stephen M. - : eScholarship, University of California, 2017
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12
Observing conversational laughter in frontotemporal dementia.
In: Journal of neurology, neurosurgery, and psychiatry, vol 88, iss 5 (2017)
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13
Data-driven regions of interest for longitudinal change in three variants of frontotemporal lobar degeneration.
In: Brain and behavior, vol 7, iss 4 (2017)
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14
Artificial grammar learning in vascular and progressive non-fluent aphasias ...
Cope, Thomas; Wilson, B; Robson, H. - : Apollo - University of Cambridge Repository, 2017
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15
Clinicopathologic correlations and neuroimaging biomarkers in primary progressive aphasia
Santos Santos, Miguel Ángel. - : Universitat Autònoma de Barcelona, 2017
In: TDX (Tesis Doctorals en Xarxa) (2017)
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16
The TMEM106B risk allele is associated with lower cortical volumes in a clinically diagnosed frontotemporal dementia cohort.
In: J Neurol Neurosurg Psychiatry (2017) (2017)
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17
Artificial grammar learning in vascular and progressive non-fluent aphasias
Cope, Thomas; Wilson, B; Robson, H. - : Elsevier, 2017. : Neuropsychologia, 2017
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18
Data-driven classification of patients with primary progressive aphasia
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19
Can MRI visual assessment differentiate the variants of primary-progressive aphasia?
Sajjadi, S. A.; Sheikh-Bahaei, N.; Cross, J.. - : American Society of Neuroradiology, 2017
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