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Feray Koc

Showing results (11-20 of 19) with videos related to

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Beyoglu Eye Journal|March 13, 2023
Comparison of Intravitreal Dexamethasone Implant and Intravitreal Ranibizumab Efficacy in Younger Patients with Branch Retinal Vein OcclusionSeda Gurakar Ozcift, Erdinc Aydin, Emine Deniz Egrilmez, et al.
International Ophthalmology|April 17, 2004
Analysis of changes in corneal shape and bulbus geometry after retinal detachment surgeryMehmet Citirik, Cosar Batman, Golge Acaroglu, et al.
The Journal of Craniofacial Surgery|December 23, 2016
A Rare Patient With Orbital Apex Syndrome, Anterior Uveitis, and Necrotizing Scleritis Due to Herpes Zoster OphthalmicusErdinc Aydin, Melike Balikoglu-Yilmaz, Seher Saritepe Imre, et al.
International Ophthalmology|December 24, 2015
Anterior segment parameters and eyelids in systemic sclerosisSevinc Sahin Atik, Feray Koc, Sirin Akin Sari, et al.
Clinical & Experimental Optometry|November 20, 2016
Choroidal and central foveal thickness in patients with scleroderma and its systemic associationsErdinc Aydin, Sevinc Atik, Feray Koc, et al.
BMC Genetics|May 22, 2007
Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1Wai-Man Chan, Caroline Andrews, Laryssa Dragan, et al.
Investigative Ophthalmology & Visual Science|March 31, 2025
Gene Identification for Ocular Congenital Cranial Motor Neuron Disorders Using Human Sequencing, Zebrafish Screening, and Protein Binding MicroarraysJulie A Jurgens, Paola M Matos Ruiz, Jessica King, et al.
Biorxiv : the Preprint Server for Biology|September 24, 2024
Gene identification for ocular congenital cranial motor neuron disorders using human sequencing, zebrafish screening, and protein binding microarraysJulie A Jurgens, Paola M Matos Ruiz, Jessica King, et al.
Cell|January 16, 2010
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidanceMax A Tischfield, Hagit N Baris, Chen Wu, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Beyoglu Eye Journal|March 13, 2023
Comparison of Intravitreal Dexamethasone Implant and Intravitreal Ranibizumab Efficacy in Younger Patients with Branch Retinal Vein OcclusionSeda Gurakar Ozcift, Erdinc Aydin, Emine Deniz Egrilmez, et al.
International Ophthalmology|April 17, 2004
Analysis of changes in corneal shape and bulbus geometry after retinal detachment surgeryMehmet Citirik, Cosar Batman, Golge Acaroglu, et al.
The Journal of Craniofacial Surgery|December 23, 2016
A Rare Patient With Orbital Apex Syndrome, Anterior Uveitis, and Necrotizing Scleritis Due to Herpes Zoster OphthalmicusErdinc Aydin, Melike Balikoglu-Yilmaz, Seher Saritepe Imre, et al.
International Ophthalmology|December 24, 2015
Anterior segment parameters and eyelids in systemic sclerosisSevinc Sahin Atik, Feray Koc, Sirin Akin Sari, et al.
Clinical & Experimental Optometry|November 20, 2016
Choroidal and central foveal thickness in patients with scleroderma and its systemic associationsErdinc Aydin, Sevinc Atik, Feray Koc, et al.
BMC Genetics|May 22, 2007
Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1Wai-Man Chan, Caroline Andrews, Laryssa Dragan, et al.
Investigative Ophthalmology & Visual Science|March 31, 2025
Gene Identification for Ocular Congenital Cranial Motor Neuron Disorders Using Human Sequencing, Zebrafish Screening, and Protein Binding MicroarraysJulie A Jurgens, Paola M Matos Ruiz, Jessica King, et al.
Biorxiv : the Preprint Server for Biology|September 24, 2024
Gene identification for ocular congenital cranial motor neuron disorders using human sequencing, zebrafish screening, and protein binding microarraysJulie A Jurgens, Paola M Matos Ruiz, Jessica King, et al.
Cell|January 16, 2010
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidanceMax A Tischfield, Hagit N Baris, Chen Wu, et al.
Pageof 2