<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11</volume><submitter>Lupo M</submitter><pubmed_abstract>Spastic paraplegia type 7 (SPG7), which represents one of the most common forms of autosomal recessive spastic paraplegia (MIM#607259), often manifests with a complicated phenotype, characterized by progressive spastic ataxia with evidence of cerebellar atrophy on brain MRI. Recent studies have documented the presence of peculiar dentate nucleus hyperintensities on T2-weighted images and frontal executive dysfunction in neuropsychological tests in SPG7 patients. Therefore, we decided to assess whether any particular MRI pattern might be specifically associated with SPG7 mutations and possibly correlated with patients' cognitive profiles. For this purpose, we evaluated six SPG7 patients, studying the cerebello-cortical network by MRI voxel-based morphometry and functional connectivity techn</pubmed_abstract><journal>Frontiers in neurology</journal><pagination>82</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7053515</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Cerebello-Cortical Alterations Linked to Cognitive and Social Problems in Patients With Spastic Paraplegia Type 7: A Preliminary Study.</pubmed_title><pmcid>PMC7053515</pmcid><pubmed_authors>Lupo M</pubmed_authors><pubmed_authors>Leggio M</pubmed_authors><pubmed_authors>Riso V</pubmed_authors><pubmed_authors>Olivito G</pubmed_authors><pubmed_authors>Siciliano L</pubmed_authors><pubmed_authors>Bozzali M</pubmed_authors><pubmed_authors>Santorelli FM</pubmed_authors><pubmed_authors>Clausi S</pubmed_authors><pubmed_authors>Silvestri G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cerebello-Cortical Alterations Linked to Cognitive and Social Problems in Patients With Spastic Paraplegia Type 7: A Preliminary Study.</name><description>Spastic paraplegia type 7 (SPG7), which represents one of the most common forms of autosomal recessive spastic paraplegia (MIM#607259), often manifests with a complicated phenotype, characterized by progressive spastic ataxia with evidence of cerebellar atrophy on brain MRI. Recent studies have documented the presence of peculiar dentate nucleus hyperintensities on T2-weighted images and frontal executive dysfunction in neuropsychological tests in SPG7 patients. Therefore, we decided to assess whether any particular MRI pattern might be specifically associated with SPG7 mutations and possibly correlated with patients' cognitive profiles. For this purpose, we evaluated six SPG7 patients, studying the cerebello-cortical network by MRI voxel-based morphometry and functional connectivity techn</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2026-05-03T14:46:13.663Z</modification><creation>2020-05-22T12:49:48Z</creation></dates><accession>S-EPMC7053515</accession><cross_references><pubmed>32161564</pubmed><doi>10.3389/fneur.2020.00082</doi></cross_references></HashMap>