Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update
Citations
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Cites background or methods from "Nomenclature and nosology for neuro..."
...The classification was modified from existing FTLD criteria (Mackenzie et al., 2009, 2010) to accommodate cases with incomplete immunohistochemistry....
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...These changes result from frontotemporal lobar degeneration (FTLD) associated with a range of heterogeneous pathologies (Mackenzie et al., 2009, 2010)....
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...Sites were asked to select cases who met modified Mackenzie criteria for FTLD (Mackenzie et al., 2009, 2010) (Table 1), and were clinically diagnosed with bvFTD, Alzheimer’s disease, vascular dementia, dementia with Lewy bodies or other neurological or psychiatric conditions at presentation....
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2,240 citations
Cites background from "Nomenclature and nosology for neuro..."
...For some tauopathies, such as tangle-predominant senile dementia (TPSD), chronic traumatic encephalopathy (CTE), or diffuse neurofibrillary tangles with calcification (DNTC), the distribution and density of tangles and the paucity of neocortical plaques must be carefully documented, since TPSD, CTE, and DNTC tangles, like AD-type NFTs, also contain both 3R and 4R tau [73–78]....
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...For FTLD-TDP (for “TDP-43”) and FTLD-FUS (for “fused in sarcoma”), immunohistochemistry for ubiquitin, alpha-internexin, TDP-43, and FUS can be of assistance [73–75]....
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..., Western blot) remains a research adjunct to neuropathologic diagnosis [73–75]....
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1,965 citations
1,699 citations
Cites methods from "Nomenclature and nosology for neuro..."
...…lobar degeneration Neuropathological diagnosis of FTLD was based on predominant involvement of the frontal and temporal lobes and characteristic immunohistochemistry for p-tau, TDP-43 and p-TDP-43 using established criteria for FTLD (Cairns et al., 2007; Bigio, 2008; Mackenzie et al., 2010)....
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References
2,387 citations
"Nomenclature and nosology for neuro..." refers background in this paper
...Recently, two studies identified mutations in the gene encoding the fused in sarcoma (FUS) protein (also known as translocated in liposarcoma, TLS), as the cause of familial amyotrophic lateral sclerosis (ALS) type 6 [5, 14]....
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2,373 citations
"Nomenclature and nosology for neuro..." refers background in this paper
...Recently, two studies identified mutations in the gene encoding the fused in sarcoma (FUS) protein (also known as translocated in liposarcoma, TLS), as the cause of familial amyotrophic lateral sclerosis (ALS) type 6 [5, 14]....
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