Expanding the neuropathological spectrum of frontotemporal lobar degenerations : review of 833 prospectively assessed dementia cases (CROSBI ID 522324)
Prilog sa skupa u časopisu | sažetak izlaganja sa skupa | međunarodna recenzija
Podaci o odgovornosti
Cairns, Nigel, J. ; Grinberg, Lea T. ; Liščić, Rajka ; Tu, Pang-hsien ; Morris, John, C.
engleski
Expanding the neuropathological spectrum of frontotemporal lobar degenerations : review of 833 prospectively assessed dementia cases
In a prospectively assessed series of dementia cases, 6.1% had frontotemporal lobar degenerations (FTLD). FTLD with ubiquitin inclusions (FTLD-U) was the most frequent FTLD accounting for 53% of cases. less common entities, argyrophilic grain disease (AGD), and hereditary diffuse leukoencephalopathy with neuroaxonal spheroids (HDLS), may also have the clinical phenotype of FTLD and should be considered in the neuropathological spectrum of FTLDs.
Frontotemporal dementia; Frontotemporal lobar degeneration; Progranulin
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Podaci o prilogu
7-7.
2006.
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objavljeno
Podaci o matičnoj publikaciji
Journal of neural transmission. Supplementum
0303-6995
Podaci o skupu
American Academy of Neuropathology Congress
predavanje
05.09.2006-07.09.2006
San Francisco (CA), Sjedinjene Američke Države