Publication:
A neurological disease mimicking central hypothyroidism: MCT8 deficiency

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dc.contributor.authorDemirbaş, Özgeçan
dc.contributor.authorEren, Erdal
dc.contributor.authorTarım, Ömer
dc.contributor.buuauthorDEMİRBAŞ, ÖZGECAN
dc.contributor.buuauthorEREN, ERDAL
dc.contributor.buuauthorTARIM, ÖMER FARUK
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentPediatri Bölümü
dc.contributor.orcid0000-0002-6922-5203
dc.contributor.orcid0000-0002-1684-1053
dc.contributor.orcid0000-0002-5322-5508
dc.contributor.researcheridJPK-3909-2023
dc.contributor.researcheridGQX-9760-2022
dc.contributor.researcheridCCU-8073-2022
dc.date.accessioned2024-07-24T10:22:45Z
dc.date.available2024-07-24T10:22:45Z
dc.date.issued2018-01-01
dc.identifier.eissn1663-2826
dc.identifier.endpage610
dc.identifier.issn1663-2818
dc.identifier.startpage610
dc.identifier.urihttps://hdl.handle.net/11452/43410
dc.identifier.volume90
dc.identifier.wos000445204104194
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherKarger
dc.relation.journalHormone Research in Paediatrics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectEndocrinology & metabolism
dc.subjectPediatrics
dc.titleA neurological disease mimicking central hypothyroidism: MCT8 deficiency
dc.typeMeeting Abstract
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Pediatri Bölümü
relation.isAuthorOfPublication1586a5c7-0ba4-4feb-a43e-24804f2f0f42
relation.isAuthorOfPublication2d1c6521-88a9-4270-9918-92f16f98006c
relation.isAuthorOfPublication73e10417-4d1e-4216-b057-4c0a0cf76dc1
relation.isAuthorOfPublication.latestForDiscovery1586a5c7-0ba4-4feb-a43e-24804f2f0f42

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