Publication: Ocular findings of oculomotor apraxia/ataxia type 1
dc.contributor.coauthor | Sönmez, Hatice Kübra | |
dc.contributor.coauthor | Gülmez Sevim, Duygu | |
dc.contributor.coauthor | Gültekin, Murat | |
dc.contributor.department | N/A | |
dc.contributor.department | N/A | |
dc.contributor.kuauthor | Şimşir, Gülşah | |
dc.contributor.kuauthor | Başak, Ayşe Nazlı | |
dc.contributor.kuprofile | Master Student | |
dc.contributor.kuprofile | Faculty Member | |
dc.contributor.schoolcollegeinstitute | Graduate School of Sciences and Engineering | |
dc.contributor.schoolcollegeinstitute | School of Medicine | |
dc.contributor.yokid | N/A | |
dc.contributor.yokid | 1512 | |
dc.date.accessioned | 2024-11-10T00:00:40Z | |
dc.date.issued | 2023 | |
dc.description.indexedby | WoS | |
dc.description.indexedby | Scopus | |
dc.description.indexedby | PubMed | |
dc.description.issue | 1 | |
dc.description.openaccess | YES | |
dc.description.publisherscope | International | |
dc.description.volume | 58 | |
dc.identifier.doi | 10.1016/j.jcjo.2022.06.006 | |
dc.identifier.issn | 0008-4182 | |
dc.identifier.link | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85148307147&doi=10.1016%2fj.jcjo.2022.06.006&partnerID=40&md5=25da20288180a0e54fb9b25f570d74f2 | |
dc.identifier.quartile | Q3 | |
dc.identifier.scopus | 2-s2.0-85148307147 | |
dc.identifier.uri | http://dx.doi.org/10.1016/j.jcjo.2022.06.006 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/15846 | |
dc.identifier.wos | 966355000001 | |
dc.keywords | Apraxias | |
dc.keywords | Ataxia | |
dc.keywords | Humans | |
dc.keywords | Mutation | |
dc.keywords | Ocular Motility Disorders | |
dc.keywords | Oculomotor Nerve Diseases | |
dc.keywords | adult | |
dc.keywords | ataxia | |
dc.keywords | best corrected visual acuity | |
dc.keywords | case report | |
dc.keywords | clinical Article | |
dc.keywords | cognitive defect | |
dc.keywords | digital radiography | |
dc.keywords | dysarthria | |
dc.keywords | dysmetria | |
dc.keywords | genetic analysis | |
dc.keywords | genetic screening | |
dc.keywords | human | |
dc.keywords | hypoalbuminemia | |
dc.keywords | Letter | |
dc.keywords | male | |
dc.keywords | Mini Mental State Examination | |
dc.keywords | motor neuropathy | |
dc.keywords | muscle atrophy | |
dc.keywords | neurologic examination | |
dc.keywords | nuclear magnetic resonance imaging | |
dc.keywords | oculomotor apraxia | |
dc.keywords | ophthalmology | |
dc.keywords | peroneus nerve paralysis | |
dc.keywords | scoliosis | |
dc.keywords | speech delay | |
dc.keywords | T2 weighted imaging | |
dc.keywords | apraxia | |
dc.keywords | ataxia | |
dc.keywords | eye movement disorder | |
dc.keywords | mutation | |
dc.keywords | oculomotor nerve disease | |
dc.language | English | |
dc.publisher | Elsevier B.V. | |
dc.source | Canadian Journal of Ophthalmology | |
dc.subject | Ophthalmology | |
dc.title | Ocular findings of oculomotor apraxia/ataxia type 1 | |
dc.type | Letter | |
dspace.entity.type | Publication | |
local.contributor.authorid | 0000-0002-4377-1804 | |
local.contributor.authorid | 0000-0001-6977-2517 | |
local.contributor.kuauthor | Şimşir, Gülşah | |
local.contributor.kuauthor | Başak, Ayşe Nazlı |