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dc.contributor.authorOzgen, B.
dc.contributor.authorOGUZ, K. K.
dc.contributor.authorSENNAROĞLU, LEVENT
dc.contributor.authorAtas, Ahmet
dc.date.accessioned2021-03-02T22:43:08Z
dc.date.available2021-03-02T22:43:08Z
dc.date.issued2009
dc.identifier.citationOzgen B., OGUZ K. K. , Atas A., SENNAROĞLU L., "Complete Labyrinthine Aplasia: Clinical and Radiologic Findings with Review of the Literature", AMERICAN JOURNAL OF NEURORADIOLOGY, cilt.30, sa.4, ss.774-780, 2009
dc.identifier.issn0195-6108
dc.identifier.othervv_1032021
dc.identifier.otherav_0e449c2b-4576-447f-a5a8-ca5acfc88397
dc.identifier.urihttp://hdl.handle.net/20.500.12627/15174
dc.identifier.urihttps://doi.org/10.3174/ajnr.a1426
dc.description.abstractBACKGROUND AND PURPOSE: Complete labyrinthine aplasia (CLA), also referred to as Michel aplasia, is a severe congenital anomaly of the inner ear, defined by the complete absence of inner ear structures. The purpose of this study was to document the imaging findings in a series of patients with CLA, with review of the literature, to better understand this anomaly.
dc.language.isoeng
dc.subjectNöroloji
dc.subjectKLİNİK NEUROLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectNÖRO-GÖRÜNTÜLEME
dc.subjectSinirbilim ve Davranış
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectRADYOLOJİ, NÜKLEER TIP ve MEDİKAL GÖRÜNTÜLEME
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNükleer Tıp
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.titleComplete Labyrinthine Aplasia: Clinical and Radiologic Findings with Review of the Literature
dc.typeMakale
dc.relation.journalAMERICAN JOURNAL OF NEURORADIOLOGY
dc.contributor.departmentHacettepe Üniversitesi , ,
dc.identifier.volume30
dc.identifier.issue4
dc.identifier.startpage774
dc.identifier.endpage780
dc.contributor.firstauthorID47304


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