Publication Detail
The publication detail shows the title, authors (with indicators showing other profiled authors), information on the publishing organization, abstract and a link to the article in PubMed. This abstract is what is used to create the fingerprint of the publication. If any grants are referenced by the publication, they will be listed here as well.
Clinical phenotypes in autopsy-confirmed Pick disease.
O Piguet; G M Halliday; W G J Reid; B Casey; R Carman; Y Huang; J H Xuereb; J R Hodges; J J Kril (Profiled Author: Hodges, John R)
Neuroscience Research Australia, Sydney, Australia. o.piguet@neura.edu.au
Neurology 2011;76(3):253-9.
BACKGROUND: Neuropathology of frontotemporal lobar degeneration is variable and relationship between the pathology and the clinical presentation remains uncertain. Abnormal deposits of hyperphosphorylated and ubiquitinated tau protein are present in 30% of cases, which include the classic presentation of Pick disease with argyrophilic, intraneuronal inclusions known as Pick bodies. This study aimed to improve sensitivity of clinicopathologic relations in cases with neuropathologically confirmed Pick disease and to identify clinical symptoms and signs predictive of disease progression. METHODS: This was a retrospective analysis of 21 cases with a pathologic diagnosis of Pick disease and sufficient clinical information to establish early presenting clinical features from 2 specialist centers, representing 70% of all cases of Pick disease identified between 1998 and 2007 in these centers. RESULTS: At presentation, 13/21 cases (62%) were clinically diagnosed with behavioral variant frontotemporal dementia (bvFTD) and 8/21 (38%) with language variant frontotemporal dementia (lvFTD) including 2 with mixed syndromes. Patients with bvFTD died on average 5 years earlier than those with lvFTD (7 years vs 12 years after disease onset). Pathologically, fewer Pick bodies were present in the frontal and inferior temporal cortices of bvFTD than lvFTD cases. In contrast, both groups showed decreased neuronal density in the dentate gyrus with increasing disease duration. CONCLUSIONS: The pathologic course of the disease in FTLD cases with Pick bodies is not uniform and disease duration can be estimated based on early clinical features. These findings have relevance as treatment options, which are likely to be pathology specific, are developed.
Scientific Context
This section shows information related to the publication - computed using the fingerprint of the publication - including related publications, related experts and related grants with fingerprints representing significant amounts of overlap between their fingerprint and this publication. The red dots indicate whether those experts or terms appear within the publication, thereby showing potential and actual connections.
Related Grants
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1.
LEE, VIRGINIA M
Frontotemporal Dementias: Genotypes and Phenotypes
15 March 2000 - 29 February 2016
NATIONAL INSTITUTE ON AGING
Total Funding: $ 21,445,858
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2.
MILLER, BRUCE L
Frontotemporal Dementia: Genes, Images, and Emotions
1 July 2001 - 31 August 2017
NATIONAL INSTITUTE ON AGING
Total Funding: $ 16,462,680
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3.
IQBAL, KHALID
Subgroups of Alzheimer Disease
15 May 2007 - 30 April 2012
NATIONAL INSTITUTE ON AGING
Total Funding: $ 1,630,946
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NeuroImage 2008;39(3):1034-40.
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