| Retinal Histology and Anatomical Landmarks in Hereditary Retinal Diseases | Asena KELEŞ ŞAHİN | 77–80 |
| Inheritance and Mutations in Hereditary Retinal Diseases | G. Ozan ÇETİN,Ebru Nevin ÇETİN | 81–84 |
| A Common Approach and Low Vision Rehabilitation in Patients with Hereditary Retinal Diseases | ESRA ŞAHLI,Aysun İDİL | 85–94 |
| Retinitis Pigmentosa; Epidemiology, Pathophysiology and Classification | Fevzi ŞENTÜRK,Mahmut DOĞRAMACI,Cengiz ARAS | 95–106 |
| Retinitis Pigmentosa: Clinical Features, Imaging and Diagnosis | Serra ARF,Mumin HOCAOĞLU | 107–112 |
| Retinitis Pigmentosa: Atypical Presentations and Systemic Associations | Havvanur BAYRAKTAR,İbrahim Arif KOYTAK | 113–122 |
| Transcorneal Electrical Stimulation and Platelet Rich Plasma Therapies in Retinitis Pigmentosa Disease | Muhammed Necati DEMİR | 123–130 |
| Retinal Transplantation, Stem Cell and Gene Therapy in Retinitis Pigmentosa | Ayşe ÖNER,Neslihan Sinim KAHRAMAN | 131–139 |
| Retinal Prosthesis in the Treatment of Retinitis Pigmentosa | Dilek GÜVEN,Semra TİRYAKİ DEMİR | 140–149 |
| Treatments Being Developed in Retinitis Pigmentosa | Mahmut KAYA,Ferit Hakan ÖNER | 150–154 |
| Congenital Stationary Night Blindness: Pathophysiology, Signs, Diagnosis and Treatment | Mücella Arıkan YORGUN | 155–158 |
| Dyschromatopsy, Achromatopsia and Blue Cone Monochromatism; Pathophysiology, Clinical Findings, Diagnosis and Treatmentand Treatment | Ender SIRAKAYA,Mustafa ATAŞ | 159–164 |
| Progressive Cone-Dystrophy, Cone-Rod Dystrophy and Rod-Cone Dystrophies | Utku LİMON,Betül İlkay SEZGİN AKÇAY | 165–172 |
| Leber Congenital Amaurosis | Mehmet Orkun SEVİK,Özlem ŞAHİN | 173–184 |
| Stargardt and Fundus Flavimaculatus; Pathophysiology, Clinical Findings, Imaging Characteristics and Diagnosis |