Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/6928
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dc.contributor.authorSemiz, Serap-
dc.contributor.authorDüzcan, Füsun-
dc.contributor.authorCandemir, M.-
dc.contributor.authorCaner, Vildan-
dc.contributor.authorThiele, S.-
dc.contributor.authorSemiz, E.-
dc.contributor.authorHiort, O.-
dc.date.accessioned2019-08-16T12:13:04Z
dc.date.available2019-08-16T12:13:04Z
dc.date.issued2009-
dc.identifier.issn0334-018X-
dc.identifier.urihttps://hdl.handle.net/11499/6928-
dc.identifier.urihttps://doi.org/10.1515/JPEM.2009.22.2.107-
dc.description.abstractAbstract Not Availableen_US
dc.language.isoenen_US
dc.publisherFreund Publishing House Ltden_US
dc.relation.ispartofJournal of Pediatric Endocrinology and Metabolismen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectparathyroid hormoneen_US
dc.subjectstimulatory guanine nucleotide binding proteinen_US
dc.subjectthyrotropinen_US
dc.subjectthyroxineen_US
dc.subjectadolescenten_US
dc.subjectAlbright syndromeen_US
dc.subjectarticleen_US
dc.subjectbrain calcificationen_US
dc.subjectcalcium metabolismen_US
dc.subjectcase reporten_US
dc.subjectcataracten_US
dc.subjectcomputer assisted tomographyen_US
dc.subjectechocardiographyen_US
dc.subjectelectrolyte disturbanceen_US
dc.subjectextrachromosomal inheritanceen_US
dc.subjectFahr diseaseen_US
dc.subjectfemaleen_US
dc.subjectfoot paresthesiaen_US
dc.subjectframeshift mutationen_US
dc.subjectgene deletionen_US
dc.subjecthand paresthesiaen_US
dc.subjecthormone resistanceen_US
dc.subjecthumanen_US
dc.subjecthyperphosphatemiaen_US
dc.subjecthypocalcemiaen_US
dc.subjectlaboratory testen_US
dc.subjectmaleen_US
dc.subjectmental deficiencyen_US
dc.subjectparathyroid hormone blood levelen_US
dc.subjectparesthesiaen_US
dc.subjectphysical examinationen_US
dc.subjectpseudohypoparathyroidismen_US
dc.subjectpseudohypoparathyroidism type Iaen_US
dc.subjectpseudopseudohypoparathyroidismen_US
dc.subjectshort statureen_US
dc.subjecttetanyen_US
dc.subjectthyrotropin blood levelen_US
dc.subjectthyroxine blood levelen_US
dc.subjectvisual system examinationen_US
dc.titlePseudohypoparathyroidism type IA (PHP-Ia): Maternally inherited GNAS gene mutationen_US
dc.typeArticleen_US
dc.identifier.volume22en_US
dc.identifier.issue2en_US
dc.identifier.startpage107
dc.identifier.startpage107en_US
dc.identifier.endpage108en_US
dc.authorid0000-0002-3973-1404-
dc.authorid0000-0003-0980-9335-
dc.identifier.doi10.1515/JPEM.2009.22.2.107-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-64249105188en_US
dc.identifier.wosWOS:000264855400002en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeArticle-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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