Publication:
Urotensin-II gene polymorphism and serum urotensin-II levels in children with Bartter syndrome

Simple item page
dc.contributor.coauthorBalat, Ayse
dc.contributor.coauthorKoc, Gulsah
dc.contributor.coauthorSoyocak, Ahu
dc.contributor.coauthorKilic, Beltinge Demircioglu
dc.contributor.coauthorKara, Mehtap
dc.contributor.coauthorBuyukcelik, Mithat
dc.contributor.coauthorNoyan, Z. Aytul
dc.contributor.coauthorAtes, Funda Seher Ozalp
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorBilge, İlmay
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2025-03-06T20:59:55Z
dc.date.issued2024
dc.description.indexedbyWOS
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.identifier.eissn1432-198X
dc.identifier.issn0931-041X
dc.identifier.issue1
dc.identifier.quartileQ1
dc.identifier.urihttps://hdl.handle.net/20.500.14288/27813
dc.identifier.volume39
dc.identifier.wos1331366600575
dc.keywordsUrotensin-II
dc.keywordsGene polymorphism
dc.keywordsSerum urotensin-II levels
dc.keywordsBartter syndrome
dc.keywordsPediatric nephrology
dc.keywordsGenetic variation
dc.keywordsRenal disorders
dc.keywordsElectrolyte imbalance
dc.keywordsHormonal regulation
dc.keywordsKidney disease biomarkers
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofPediatric Nephrology
dc.subjectPediatrics
dc.subjectUrology and nephrology
dc.titleUrotensin-II gene polymorphism and serum urotensin-II levels in children with Bartter syndrome
dc.typeMeeting Abstract
dspace.entity.typePublication
local.contributor.kuauthorBilge, İlmay
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
relation.isOrgUnitOfPublicationd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

Files

Collections

Publications without Fulltext