Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations.
Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations.
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DOI:
10.1007/s00401-008-0460-5
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发表时间:
2009-01
影响因子:
12.7
通讯作者:
Mann DM
中科院分区:
文献类型:
--
作者:
Mackenzie IR;Neumann M;Bigio EH;Cairns NJ;Alafuzoff I;Kril J;Kovacs GG;Ghetti B;Halliday G;Holm IE;Ince PG;Kamphorst W;Revesz T;Rozemuller AJ;Kumar-Singh S;Akiyama H;Baborie A;Spina S;Dickson DW;Trojanowski JQ;Mann DM
The neuropathology associated with the clinical entities frontotemporal dementia (FTD, behavioral variant FTD), progressive non-Xuent aphasia (PNFA) and semantic dementia (SD), is heterogeneous with the common feature being a relatively selective degeneration of the frontal and temporal lobes (frontotemporal lobar degeneration, FTLD). As in other neurodegenerative conditions, most pathological subtypes of FTLD are characterized by specific kinds of intracellular protein inclusions. In the past few decades, the biochemical composition of many of these inclusion bodies has been determined. There is a growing trend to classify FTLD based on the presumed molecular defect, in the belief that this most closely reXects the underlying pathogenic process and because many of the eponymous and descriptively named syndromes of the past are now known to have imperfect clinicopathological correlation.
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影响因子:
12.7
作者:
Nakashima-Yasuda, Hanae;Uryu, Kunihiro;Trojanowski, John Q.
通讯作者:
Trojanowski, John Q.
影响因子:
12.7
作者:
Roeber, Sigrun;Mackenzie, Ian R. A.;Neumann, Manuela
通讯作者:
Neumann, Manuela
DOI:
10.1097/nen.0b013e31817713b5
发表时间:
2008-06-01
影响因子:
3.2
作者:
Uryu, Kunihiro;Nakashima-Yasuda, Hanae;Neumann, Manuela
通讯作者:
Neumann, Manuela
影响因子:
11.2
作者:
Amador-Ortiz, Catalina;Lin, Wen-Lang;Dickson, Dennis W.
通讯作者:
Dickson, Dennis W.
DOI:
10.1097/nen.0b013e3181567f02
发表时间:
2007-10-01
影响因子:
3.2
作者:
Holm, Ida Elisabeth;Englund, Elisabet;Isaacs, Adrian M.
通讯作者:
Isaacs, Adrian M.