<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Kawles A</submitter><funding>NIA NIH HHS</funding><funding>NIDCD NIH HHS</funding><funding>NINDS NIH HHS</funding><pubmed_abstract>&lt;h4>Objective&lt;/h4>Frontotemporal lobar degenerations (FTLD)-TDP type C (TDP-C) is distinguished from other FTLD-TDP subtypes by 3 unique features: (1) invariable onset in the anterior temporal lobe (ATL), (2) phosphorylated TDP-43 (pTDP) neurites in cortex, and (3) colocalization of all pTDP deposits with annexin A11 (ANXA11). This article provides a whole-brain anatomical account of TDP-C disease progression in relation to clinical, imaging, and neuropathologic patterns.&lt;h4>Methods&lt;/h4>Thirty-two cases with TDP-C were studied, including neuropathologic findings and longitudinal magnetic resonance imaging. In 6 of these cases, cortical and subcortical areas were analyzed using whole hemisphere sections. Five control cases were used for comparison.&lt;h4>Results&lt;/h4>Progression was reconstruct</pubmed_abstract><journal>Annals of neurology</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12704552</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Anatomical Progression of Neuropathology in FTLD-TDP Type C and Linkage to Annexin A11.</pubmed_title><pmcid>PMC12704552</pmcid><funding_grant_id>R56 AG075600</funding_grant_id><funding_grant_id>R01 AG091388</funding_grant_id><funding_grant_id>R01 AG077444</funding_grant_id><funding_grant_id>P30 AG072977</funding_grant_id><funding_grant_id>F31 AG094137</funding_grant_id><funding_grant_id>T32 AG020506</funding_grant_id><funding_grant_id>R01 DC008552</funding_grant_id><funding_grant_id>R01 NS075075</funding_grant_id><funding_grant_id>P30 AG013854</funding_grant_id><pubmed_authors>Barbieri E</pubmed_authors><pubmed_authors>Nelson C</pubmed_authors><pubmed_authors>Gefen T</pubmed_authors><pubmed_authors>Geula C</pubmed_authors><pubmed_authors>Mesulam MM</pubmed_authors><pubmed_authors>Castellani R</pubmed_authors><pubmed_authors>Kawles A</pubmed_authors><pubmed_authors>Ayala I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Anatomical Progression of Neuropathology in FTLD-TDP Type C and Linkage to Annexin A11.</name><description>&lt;h4>Objective&lt;/h4>Frontotemporal lobar degenerations (FTLD)-TDP type C (TDP-C) is distinguished from other FTLD-TDP subtypes by 3 unique features: (1) invariable onset in the anterior temporal lobe (ATL), (2) phosphorylated TDP-43 (pTDP) neurites in cortex, and (3) colocalization of all pTDP deposits with annexin A11 (ANXA11). This article provides a whole-brain anatomical account of TDP-C disease progression in relation to clinical, imaging, and neuropathologic patterns.&lt;h4>Methods&lt;/h4>Thirty-two cases with TDP-C were studied, including neuropathologic findings and longitudinal magnetic resonance imaging. In 6 of these cases, cortical and subcortical areas were analyzed using whole hemisphere sections. Five control cases were used for comparison.&lt;h4>Results&lt;/h4>Progression was reconstruct</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-06-06T03:42:26.875Z</modification><creation>2026-05-25T03:08:09.284Z</creation></dates><accession>S-EPMC12704552</accession><cross_references><pubmed>41294076</pubmed><doi>10.1002/ana.78095</doi></cross_references></HashMap>