<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>55(6)</volume><submitter>Gokcay Canpolat A</submitter><pubmed_abstract>&lt;h4>Background/aim&lt;/h4>To describe Graves' Disease (GD) associated with COVID-19 infection (COVID) or its vaccines (VAC) and to compare the clinical presentations, laboratory parameters, and short-term clinical course of the disease among different etiology groups (COVID, VAC, and GD control).&lt;h4>Materials and methods&lt;/h4>Included in this multicenter matched case-control, retrospective cohort study were 239 patients with newly diagnosed (n = 196) or recurrent GD (n = 43) associated with COVID (n = 79) or VAC (n = 160). Each case was matched (1:1) with a control who had been diagnosed with GD prior to COVID.&lt;h4>Results&lt;/h4>The median age of the entire group was 42 years (female:male = 137:102). Both the COVID (4.6-fold) and VAC (4.1-fold) groups demonstrated higher TSH receptor antibody (TR</pubmed_abstract><journal>Turkish journal of medical sciences</journal><pagination>1381-1393</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12779019</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Clinical characteristics of Graves' disease following COVID-19 infection or vaccination: a multicenter case-control study.</pubmed_title><pmcid>PMC12779019</pmcid><pubmed_authors>Kara B</pubmed_authors><pubmed_authors>Balos Toruner F</pubmed_authors><pubmed_authors>Aydemir M</pubmed_authors><pubmed_authors>Cansu GB</pubmed_authors><pubmed_authors>Yalcin M</pubmed_authors><pubmed_authors>Polat SB</pubmed_authors><pubmed_authors>Alagol F</pubmed_authors><pubmed_authors>Omma T</pubmed_authors><pubmed_authors>Elhan AH</pubmed_authors><pubmed_authors>Yazici D</pubmed_authors><pubmed_authors>Alphan Uc Z</pubmed_authors><pubmed_authors>Gokcay Canpolat A</pubmed_authors><pubmed_authors>Bostan H</pubmed_authors><pubmed_authors>Oguz A</pubmed_authors><pubmed_authors>Batman A</pubmed_authors><pubmed_authors>Faki S</pubmed_authors><pubmed_authors>Asik M</pubmed_authors><pubmed_authors>Ucan B</pubmed_authors><pubmed_authors>Evren B</pubmed_authors><pubmed_authors>Ugur K</pubmed_authors><pubmed_authors>Kubat Uzum A</pubmed_authors><pubmed_authors>Mutlu U</pubmed_authors><pubmed_authors>Gurlek A</pubmed_authors><pubmed_authors>Ok AM</pubmed_authors><pubmed_authors>Sahin M</pubmed_authors><pubmed_authors>Ince N</pubmed_authors><pubmed_authors>Cesur M</pubmed_authors><pubmed_authors>Iliksu Gozu H</pubmed_authors><pubmed_authors>Yildiz BO</pubmed_authors><pubmed_authors>Karakilic E</pubmed_authors><pubmed_authors>Cakir B</pubmed_authors><pubmed_authors>Cakal E</pubmed_authors><pubmed_authors>Yilmaz M</pubmed_authors><pubmed_authors>Erdogan MF</pubmed_authors><pubmed_authors>Akcay S</pubmed_authors><pubmed_authors>Agbaht K</pubmed_authors><pubmed_authors>Erturk MS</pubmed_authors><pubmed_authors>Yorulmaz G</pubmed_authors><pubmed_authors>Saygili ES</pubmed_authors><pubmed_authors>Sah Unal T</pubmed_authors><pubmed_authors>Anil C</pubmed_authors><pubmed_authors>Unal MC</pubmed_authors><pubmed_authors>Ersoy R</pubmed_authors><pubmed_authors>Kayhan Y</pubmed_authors><pubmed_authors>Topaloglu O</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical characteristics of Graves' disease following COVID-19 infection or vaccination: a multicenter case-control study.</name><description>&lt;h4>Background/aim&lt;/h4>To describe Graves' Disease (GD) associated with COVID-19 infection (COVID) or its vaccines (VAC) and to compare the clinical presentations, laboratory parameters, and short-term clinical course of the disease among different etiology groups (COVID, VAC, and GD control).&lt;h4>Materials and methods&lt;/h4>Included in this multicenter matched case-control, retrospective cohort study were 239 patients with newly diagnosed (n = 196) or recurrent GD (n = 43) associated with COVID (n = 79) or VAC (n = 160). Each case was matched (1:1) with a control who had been diagnosed with GD prior to COVID.&lt;h4>Results&lt;/h4>The median age of the entire group was 42 years (female:male = 137:102). Both the COVID (4.6-fold) and VAC (4.1-fold) groups demonstrated higher TSH receptor antibody (TR</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2026-06-06T12:45:46.659Z</modification><creation>2026-05-30T03:11:38.411Z</creation></dates><accession>S-EPMC12779019</accession><cross_references><pubmed>41509944</pubmed><doi>10.55730/1300-0144.6096</doi></cross_references></HashMap>