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|Jump to main content jump to navigation nature. Com homepage publications a-z index browse by subject my account e-alert sign up register subscribe login cart search advanced search journal home > advance online publication > review > full text > box 1 box 1 | timeline of discoveries in the molecular pathogenesis of ftd from the following article: advances in understanding the molecular basis of frontotemporal dementia rosa rademakers, manuela neumann & ian r. Mackenzie nature reviews neurology advance online publication published online 26 june 2012 doi:10. 1038/nrneurol. cheap generic viagra generic viagra online cheap viagra online cheap viagra online cheap generic viagra buy cheap viagra cheap viagra fast shipping overnight viagra online buy viagra online buy viagra online 2012. 117 back to article | next box 1892: arnold pick describes lobar atrophy in a patient with presenile dementia and aphasia 147 1911: alois alzheimer characterizes pick bodies using silver stains 148 1960s: descriptions of psp and cbd clinicopathological syndromes 149, 150 1974: different pathological subtypes of pid described 151 mid-1980s–early 1990s: identification of tau as major component of pathological lesions in alzheimer disease, pid, psp and cbd 152 1990: description of ftd cases without specific histopathology, termed dldh 153 mid-1990s: identification of ftld-u, a subset of ftd with ubiquitin-immunoreactive inclusions 154 1998: mutations in the microtubule-associated protein tau gene (mapt) identified in some families with ftd and parkinsonism genetically linked to chromosome 17 10, 11, 12 2004–2006: recognition that most cases of dldh are really ftld-u, and that ftld-u is the most common ftd-associated pathology 34 2006: description of different patterns of ftld-u that correlate with clinical phenotypes, genetic abnormalities and biochemical properties of inclusions 116, 118 2006: discovery that mutations in the progranulin gene (grn) cause autosomal dominant ftd and explain all remaining chromosome 17-linked families 15, 16 2006: tdp-43 identified as pathological protein in most cases of ftld-u and als 35, 36 2008: identification of a subset of ftld-u cases that lack tdp-43-immunoreactive pathology, termed atypical ftld-u, or aftld-u 155, 156 2009: discovery that most cases of tau-negative and tdp-43-negative ftld have fus-immunoreactive pathology (ftld-fus) 39, 40, 41 2011: discovery that ftld-fus shows accumulation of other fet protein family members taf15 and ews 42 2011: ftd and als associated with a gene defect on chromosome 9p identified as a repeat expansion in c9orf72 28, 29 abbreviations: als, amyotrophic lateral sclerosis; cbd, corticobasal degeneration; dldh, dementia lacking distinct histopathology; ftd, frontotemp. |