<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rudra S</submitter><funding>NIDDK NIH HHS</funding><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><funding>NIH</funding><pagination>1408-1410.e2</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8792097</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(6)</volume><pubmed_abstract>Very early onset inflammatory bowel disease (VEO-IBD), diagnosed &lt;6 years old, can be genetically and phenotypically distinct and more refractory than older-onset IBD. Identified causal monogenic defects have been targeted therapeutically in a small subset of VEO-IBD&lt;sup>1&lt;/sup>; however, for most of these children, treatment strategies, such as phenotypic profiles, are critically needed to improve outcomes.</pubmed_abstract><journal>Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association</journal><pubmed_title>Ruxolitinib: Targeted Approach for Treatment of Autoinflammatory Very Early Onset Inflammatory Bowel Disease.</pubmed_title><pmcid>PMC8792097</pmcid><funding_grant_id>R01 DK111843</funding_grant_id><funding_grant_id>K23 DK119585</funding_grant_id><funding_grant_id>R01 DK127044</funding_grant_id><pubmed_authors>Shaul E</pubmed_authors><pubmed_authors>Patel T</pubmed_authors><pubmed_authors>Dawany N</pubmed_authors><pubmed_authors>Sullivan KE</pubmed_authors><pubmed_authors>Moore A</pubmed_authors><pubmed_authors>Conrad M</pubmed_authors><pubmed_authors>Behrens E</pubmed_authors><pubmed_authors>Canavan MC</pubmed_authors><pubmed_authors>Kelsen JR</pubmed_authors><pubmed_authors>Rudra S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ruxolitinib: Targeted Approach for Treatment of Autoinflammatory Very Early Onset Inflammatory Bowel Disease.</name><description>Very early onset inflammatory bowel disease (VEO-IBD), diagnosed &lt;6 years old, can be genetically and phenotypically distinct and more refractory than older-onset IBD. Identified causal monogenic defects have been targeted therapeutically in a small subset of VEO-IBD&lt;sup>1&lt;/sup>; however, for most of these children, treatment strategies, such as phenotypic profiles, are critically needed to improve outcomes.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jun</publication><modification>2025-04-18T17:46:56.312Z</modification><creation>2025-04-07T05:20:47.065Z</creation></dates><accession>S-EPMC8792097</accession><cross_references><pubmed>34329777</pubmed><doi>10.1016/j.cgh.2021.07.040</doi></cross_references></HashMap>