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Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

dc.contributor.authorAydin, Murat
dc.contributor.authorGÜRAN, TÜLAY
dc.contributor.authorAkberzade, Azad
dc.contributor.authorAbaci, Ayhan
dc.contributor.authorDemir, Korcan
dc.contributor.authorBober, Ece
dc.contributor.authorOzbek, Mehmet Nuri
dc.contributor.authorPOYRAZOĞLU, Şükran
dc.contributor.authorKara, Cengiz
dc.contributor.authorKardelen, Asli
dc.contributor.authorTarim, Omer
dc.contributor.authorEren, Erdal
dc.contributor.authorHatipoglu, Nihal
dc.contributor.authorBuyukinan, Muammer
dc.contributor.authorAkyurek, Nesibe
dc.contributor.authorCetinkaya, Semra
dc.contributor.authorBayramoglu, Elvan
dc.contributor.authorEklioglu, Beray Selver
dc.contributor.authorUcakturk, Ahmet
dc.contributor.authorAbali, Saygin
dc.contributor.authorGoksen, Damla
dc.contributor.authorKor, Yilmaz
dc.contributor.authorUnal, Edip
dc.contributor.authorEsen, Ihsan
dc.contributor.authorYildirim, Ruken
dc.contributor.authorAkin, Onur
dc.contributor.authorCayir, Atilla
dc.contributor.authorDilek, Emine
dc.contributor.authorKirel, Birgul
dc.contributor.authorAnik, Ahmet
dc.contributor.authorCatli, Gonul
dc.contributor.authorBerberoglu, Merih
dc.contributor.authorBAŞ, Firdevs
dc.contributor.authorSiklar, Zeynep
dc.contributor.authorDEMİRCİOĞLU, SERAP
dc.contributor.authorBEREKET, ABDULLAH
dc.date.accessioned2021-03-02T18:14:11Z
dc.date.available2021-03-02T18:14:11Z
dc.date.issued2020
dc.identifier.citationSiklar Z., DEMİRCİOĞLU S., BEREKET A., BAŞ F., GÜRAN T., Akberzade A., Abaci A., Demir K., Bober E., Ozbek M. N. , et al., "Nationwide Turkish Cohort Study of Hypophosphatemic Rickets", JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, cilt.12, sa.2, ss.150-159, 2020
dc.identifier.issn1308-5727
dc.identifier.othervv_1032021
dc.identifier.otherav_39945399-0da8-48a9-b351-511a1e13a471
dc.identifier.urihttp://hdl.handle.net/20.500.12627/4738
dc.identifier.urihttps://doi.org/10.4274/jcrpe.galenos.2019.2019.0098
dc.description.abstractObjective: Hypophosphatemic rickets (HR) is a rare renal phosphate-wasting disorder, which is usually X-linked and is commonly caused by PHEX mutations. The treatment and follow-up of HR is challenging due to imperfect treatment options.
dc.language.isoeng
dc.subjectPEDİATRİ
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectİç Hastalıkları
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.titleNationwide Turkish Cohort Study of Hypophosphatemic Rickets
dc.typeMakale
dc.relation.journalJOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY
dc.contributor.departmentAnkara Üniversitesi , ,
dc.identifier.volume12
dc.identifier.issue2
dc.identifier.startpage150
dc.identifier.endpage159
dc.contributor.firstauthorID2273430


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