Neslihan Sinim Kahraman

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 12

Top Topics

Optical Coherence Tomography

Diabetic Retinopathy

Top Venues

Turkish journal of ophthalmology

Ophthalmic genetics

Clinical genetics

European journal of ophthalmology

This page only lists publications with an associated author ORCID identifier.

Publications

Ayşe Öner, Neslihan Sinim Kahraman
Evaluation of Full-Field Stimulus Threshold Test Results in Retinitis Pigmentosa: Relationship with Full-Field Electroretinography, Multifocal Electroretinography, Optical Coherence Tomography, and Visual Field. Turkish journal of ophthalmology 54 (1) (2024)
Büşra Özgüç Çalışkan, Kubra Uslu, Neslihan Sinim Kahraman, Kuddusi Erkilic, Ayşe Öner, Munis Dündar
Beyond the phenotype: Exploring inherited retinal diseases with targeted next-generation sequencing in a Turkish cohort. Clinical genetics (2024)
Neslihan Sinim Kahraman, Büşra Özgüç Çalışkan, Nefise Kandemir, Ayşe Öner, Munis Dündar, Yusuf Ozkul
ABCA4 variant screening in a Turkish cohort with Stargardt disease. Ophthalmic genetics (2024)
Neslihan Sinim Kahraman, Büşra Özgüç Çalışkan, Nefise Kandemir, Ayşe Öner, Munis Dündar, Yusuf Ozkul
ABCA4 variant screening in a Turkish cohort with Stargardt disease. Ophthalmic genetics 45 (2) (2024)
Neslihan Sinim Kahraman, Büşra Özgüç Çalışkan, Nefise Kandemir, Ayşe Öner, Munis Dündar, Yusuf Ozkul
ABCA4 variant screening in a Turkish cohort with Stargardt disease. Ophthalmic genetics 45 (2) (2024)
Neslihan Sinim Kahraman, Büşra Özgüç Çalışkan, Nefise Kandemir, Ayşe Öner, Munis Dündar, Yusuf Ozkul
ABCA4 variant screening in a Turkish cohort with Stargardt disease. Ophthalmic genetics 45 (2) (2024)
Ayşe Öner, Neslihan Sinim Kahraman, Mehmet Orkun Sevik, Kübra Kelek Tülü, Özlem Şahin, Saliha Özsoy
Emotional State Evaluation of Retinitis Pigmentosa Patients with the Beck Depression Inventory. Turkish journal of ophthalmology 54 (4) (2024)
Büşra Özgüç Çalışkan, Kubra Uslu, Neslihan Sinim Kahraman, Kuddusi Erkilic, Ayşe Öner, Munis Dündar
Beyond the phenotype: Exploring inherited retinal diseases with targeted next-generation sequencing in a Turkish cohort. Clinical genetics 106 (3) (2024)
Ayşe Öner, Neslihan Sinim Kahraman
Evaluation of Full-Field Stimulus Threshold Test Results in Retinitis Pigmentosa: Relationship with Full-Field Electroretinography, Multifocal Electroretinography, Optical Coherence Tomography, and Visual Field. Turkish journal of ophthalmology 54 (1) (2024)
Ayşe Öner, Neslihan Sinim Kahraman
Evaluation of Full-Field Stimulus Threshold Test Results in Retinitis Pigmentosa: Relationship with Full-Field Electroretinography, Multifocal Electroretinography, Optical Coherence Tomography, and Visual Field. Turkish journal of ophthalmology 54 (1) (2024)
Neslihan Sinim Kahraman, Ayşe Öner, Yusuf Ozkul, Munis Dündar
Frequency of RPE65 Gene Mutation in Patients with Hereditary Retinal Dystrophy. Turkish journal of ophthalmology 52 (4) (2022)
Neslihan Sinim Kahraman, Ayşe Öner
Umbilical cord-derived mesenchymal stem cell implantation in patients with optic atrophy. European journal of ophthalmology 31 (6) (2020)