<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Whitwell JL</submitter><funding>NICHD NIH HHS</funding><funding>NIA NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>NINDS NIH HHS</funding><pagination>813-20</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2677544</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>72(9)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>To compare patterns of gray matter loss in subjects with mutations in the progranulin (PGRN) gene to subjects with mutations in the microtubule-associated protein tau (MAPT) gene.&lt;h4>Methods&lt;/h4>We identified all subjects seen at the Mayo Clinic, Rochester, MN, who had screened positive for mutations in PGRN or MAPT and had a head MRI. Twelve cases with mutations in the PGRN gene were matched by time from disease onset to scan to 12 subjects with mutations in the MAPT gene. Voxel-based morphometry was used to assess patterns of gray matter loss in the PGRN and MAPT groups compared to a control cohort, and compared to each other. MAPT subjects were younger than the PGRN subjects; therefore, each group was also compared to a specific age-matched control group.&lt;h4>Results&lt;/h</pubmed_abstract><journal>Neurology</journal><pubmed_title>Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN.</pubmed_title><pmcid>PMC2677544</pmcid><funding_grant_id>C06 RR018898</funding_grant_id><funding_grant_id>P50-AG16574</funding_grant_id><funding_grant_id>P50 NS40256</funding_grant_id><funding_grant_id>K12 HD49078</funding_grant_id><funding_grant_id>U01-AG06786</funding_grant_id><funding_grant_id>R01-AG11378</funding_grant_id><pubmed_authors>Baker M</pubmed_authors><pubmed_authors>Wszolek ZK</pubmed_authors><pubmed_authors>Josephs KA</pubmed_authors><pubmed_authors>Whitwell JL</pubmed_authors><pubmed_authors>Jack CR</pubmed_authors><pubmed_authors>Rademakers R</pubmed_authors><pubmed_authors>Ivnik RJ</pubmed_authors><pubmed_authors>Knopman DS</pubmed_authors><pubmed_authors>Boeve BF</pubmed_authors><pubmed_authors>Senjem ML</pubmed_authors><pubmed_authors>Petersen RC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN.</name><description>&lt;h4>Objective&lt;/h4>To compare patterns of gray matter loss in subjects with mutations in the progranulin (PGRN) gene to subjects with mutations in the microtubule-associated protein tau (MAPT) gene.&lt;h4>Methods&lt;/h4>We identified all subjects seen at the Mayo Clinic, Rochester, MN, who had screened positive for mutations in PGRN or MAPT and had a head MRI. Twelve cases with mutations in the PGRN gene were matched by time from disease onset to scan to 12 subjects with mutations in the MAPT gene. Voxel-based morphometry was used to assess patterns of gray matter loss in the PGRN and MAPT groups compared to a control cohort, and compared to each other. MAPT subjects were younger than the PGRN subjects; therefore, each group was also compared to a specific age-matched control group.&lt;h4>Results&lt;/h</description><dates><release>2009-01-01T00:00:00Z</release><publication>2009 Mar</publication><modification>2025-04-05T13:13:17.352Z</modification><creation>2019-03-27T00:22:10Z</creation></dates><accession>S-EPMC2677544</accession><cross_references><pubmed>19255408</pubmed><doi>10.1212/01.wnl.0000343851.46573.67</doi></cross_references></HashMap>