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2. A multidisciplinary approach to inherited retinal dystrophies from diagnosis to initial care: a narrative review with inputs from clinical practice

4. Comparison Between Monofocal and Aspheric Monofocal Intraocular Lens With Higher Order Aspheric Optic in Pediatric Patients: Early Outcomes.

5. Effectiveness of Defocus Incorporated Multiple Segments in Slowing Myopia Progression in Pediatric Patients as a Function of Age: Three-Year Follow-Up.

6. Genotypic and phenotypic characterization of a cohort of patients affected by rod CNG channel-associated retinitis pigmentosa

7. Voretigene neparvovec for inherited retinal dystrophy due to RPE65mutations: a scoping review of eligibility and treatment challenges from clinical trials to real practice

12. Pathogenicity of new BEST1 variants identified in Italian patients with best vitelliform macular dystrophy assessed by computational structural biology

14. Congenital heart defects in CTNNB1 syndrome: Raising clinical awareness.

16. A Novel Autosomal Recessive Variant of the NRL Gene Causing Enhanced S-Cone Syndrome: A Morpho-Functional Analysis of Two Unrelated Pediatric Patients

17. Narrative medicine to investigate the quality of life and emotional impact of inherited retinal disorders through the perspectives of patients, caregivers and clinicians: an Italian multicentre project

19. Genetics of Inherited Retinal Diseases in Understudied Ethnic Groups in Italian Hospitals

21. Analysis of tear film in cystinosis patients treated with topical viscous cysteamine hydrochloride (Cystadrops

22. RPE65-Associated Retinopathies in the Italian Population: A Longitudinal Natural History Study

25. Care Pathway of RPE65-Related Inherited Retinal Disorders from Early Symptoms to Genetic Counseling: A Multicenter Narrative Medicine Project in Italy

30. Care Pathway of RPE65-Related Inherited Retinal Disorders from Early Symptoms to Genetic Counseling: A Multicenter Narrative Medicine Project in Italy

31. Expanding the Clinical and Genetic Spectrum of RAB28-Related Cone-Rod Dystrophy: Pathogenicity of Novel Variants in Italian Families

32. Treatment of Advanced Coats' Disease With Combination Therapy of Laser Photocoagulation, Intravitreal Ranibizumab, and Sub-Tenon Methylprednisolone Acetate.

34. CRB1 -Related Cystic Maculopathy in Twins Conceived Through Heterologous Fertilization With Variant-Carrying Oocytes

36. Early neurodevelopmental characterization in children with cobalamin C/defect

37. Dexamethasone Intravitreal Implant (Ozurdex) in Paediatric Patients with Non-infectious Intermediate Uveitis and Related Cystoid Macular Oedema: Evaluation of Macular Morphology and Function with Six-month Follow-up; a Deeper Role of MfERG?

38. Additional file 1: of Mutation profile of BBS genes in patients with Bardetâ Biedl syndrome: an Italian study

39. Additional file 2: of Mutation profile of BBS genes in patients with Bardetâ Biedl syndrome: an Italian study

40. MOESM2 of Pathogenicity of new BEST1 variants identified in Italian patients with best vitelliform macular dystrophy assessed by computational structural biology

43. Additional file 4: of Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

44. Additional file 7: of Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

45. Additional file 6: of Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

46. Additional file 5: of Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

47. Additional file 1: of Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

48. Additional file 3: of Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

50. Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

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