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Retrospective Evaluation of Patients Diagnosed with Osteogenesis Imperfecta

dc.contributor.authorEren, Erdal
dc.contributor.authorSaglam, Halil
dc.contributor.authorTarim, Omer
dc.contributor.authorAslan, Mustafa Törehan
dc.date.accessioned2021-03-03T08:09:38Z
dc.date.available2021-03-03T08:09:38Z
dc.identifier.citationAslan M. T. , Eren E., Saglam H., Tarim O., "Retrospective Evaluation of Patients Diagnosed with Osteogenesis Imperfecta", GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS, cilt.15, ss.1-5, 2017
dc.identifier.othervv_1032021
dc.identifier.otherav_15fc116b-8381-4d29-a3ea-fdf5f50de63c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/20134
dc.identifier.urihttps://doi.org/10.4274/jcp.26234
dc.description.abstractIntroduction: Osteogenesis imperfecta (OI) is a hereditary disease that impairs the quality of life by frequent bone fractures. The objective of our study is to retrospectively evaluate patients diagnosed with OI and to come up with helpful data that will assist developing new diagnosis and treatment protocols.
dc.language.isoeng
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.titleRetrospective Evaluation of Patients Diagnosed with Osteogenesis Imperfecta
dc.typeMakale
dc.relation.journalGUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS
dc.contributor.departmentBursa Uludağ Üniversitesi , ,
dc.identifier.volume15
dc.identifier.startpage1
dc.identifier.endpage5
dc.contributor.firstauthorID717863


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