<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ban R</submitter><funding>Special Research Fund for Central Universities, Peking Union Medical College</funding><funding>Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences</funding><pagination>321</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12839809</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(2)</volume><pubmed_abstract>&lt;b>Background/Objectives&lt;/b>&lt;b>:&lt;/b> Anti-mGluR1 encephalitis is a rare form of autoimmune encephalitis predominantly manifesting as acute/subacute cerebellar ataxia. We describe a newly diagnosed case series from our center and conduct a comprehensive review of reported cases worldwide to compare clinical manifestations, treatment options, and outcomes. &lt;b>Methods:&lt;/b> We consecutively identified 11 patients at Peking Union Medical College Hospital, and additionally extracted clinical data from 42 previously published cases identified via PubMed and Google Scholar (search updated to 1 August 2025). Demographics, phenotypes, laboratory findings, imaging, treatment, and outcomes were systematically summarized. This pooled review was not prospectively registered, and extracted data from 21 p</pubmed_abstract><journal>Diagnostics (Basel, Switzerland)</journal><pubmed_title>Clinical Phenotypes and Prognosis of Anti-mGluR1 Encephalitis: A Single-Center Case Series and Comprehensive Literature Review.</pubmed_title><pmcid>PMC12839809</pmcid><funding_grant_id>3332024007</funding_grant_id><funding_grant_id>2021-I2M-1-003</funding_grant_id><pubmed_authors>Ren H</pubmed_authors><pubmed_authors>Jiang J</pubmed_authors><pubmed_authors>Liu M</pubmed_authors><pubmed_authors>Guan H</pubmed_authors><pubmed_authors>Shen D</pubmed_authors><pubmed_authors>Ban R</pubmed_authors><pubmed_authors>Fan S</pubmed_authors><pubmed_authors>Yu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical Phenotypes and Prognosis of Anti-mGluR1 Encephalitis: A Single-Center Case Series and Comprehensive Literature Review.</name><description>&lt;b>Background/Objectives&lt;/b>&lt;b>:&lt;/b> Anti-mGluR1 encephalitis is a rare form of autoimmune encephalitis predominantly manifesting as acute/subacute cerebellar ataxia. We describe a newly diagnosed case series from our center and conduct a comprehensive review of reported cases worldwide to compare clinical manifestations, treatment options, and outcomes. &lt;b>Methods:&lt;/b> We consecutively identified 11 patients at Peking Union Medical College Hospital, and additionally extracted clinical data from 42 previously published cases identified via PubMed and Google Scholar (search updated to 1 August 2025). Demographics, phenotypes, laboratory findings, imaging, treatment, and outcomes were systematically summarized. This pooled review was not prospectively registered, and extracted data from 21 p</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-09T03:20:41.758Z</modification><creation>2026-06-09T03:12:02.388Z</creation></dates><accession>S-EPMC12839809</accession><cross_references><pubmed>41594296</pubmed><doi>10.3390/diagnostics16020321</doi></cross_references></HashMap>