213 results on '"Iarossi, Giancarlo"'
Search Results
2. A multidisciplinary approach to inherited retinal dystrophies from diagnosis to initial care: a narrative review with inputs from clinical practice
3. Genetic characteristics of 234 Italian patients with macular and cone/cone-rod dystrophy
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
8. Ocular manifestations and viral shedding in tears of pediatric patients with coronavirus disease 2019: a preliminary report
9. A Next Generation Sequencing custom gene panel as first line diagnostic tool for atypical cases of syndromic obesity: Application in a case of Alström syndrome
10. Refractive outcome of keratoconus treated by big-bubble deep anterior lamellar keratoplasty in pediatric patients: two-year follow-up comparison between mechanical trephine and femtosecond laser assisted techniques
11. Iontophoretic Transepithelial Collagen Cross-Linking Versus Epithelium-Off Collagen Cross-Linking in Pediatric Patients: 3-Year Follow-Up
12. Pathogenicity of new BEST1 variants identified in Italian patients with best vitelliform macular dystrophy assessed by computational structural biology
13. Mutation profile of BBS genes in patients with Bardet–Biedl syndrome: an Italian study
14. Congenital heart defects in CTNNB1 syndrome: Raising clinical awareness.
15. Superficial and Deep Capillary Plexuses: Potential Biomarkers of Focal Retinal Defects in Eyes Affected by Macular Idiopatic Epiretinal Membranes? A Pilot Study
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
18. Four years of corneal keratoplasty in Italian paediatric patients: indications and clinical outcomes
19. Genetics of Inherited Retinal Diseases in Understudied Ethnic Groups in Italian Hospitals
20. Optical coherence tomography and electrophysiological findings in torpedo maculopathy
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
23. Comparative analysis of visual outcomes of multifocal and monofocal intraocular lenses in congenital cataract surgery
24. Treatment of Advanced Coats' Disease With Combination Therapy of Laser Photocoagulation, Intravitreal Ranibizumab, and Sub-Tenon Methylprednisolone Acetate
25. Care Pathway of RPE65-Related Inherited Retinal Disorders from Early Symptoms to Genetic Counseling: A Multicenter Narrative Medicine Project in Italy
26. Simultaneous transepithelial topographic-guided laser and cross-linking to correct irregular astigmatism in a pediatric patient.
27. Simultaneous transepithelial topographic-guided laser and cross-linking to correct irregular astigmatism in a pediatric patient
28. Inner Macular Changes in Fellow Eye of Patients With Unilateral Idiopathic Epiretinal Membrane
29. Blue Cone Monochromatism with Foveal Hypoplasia Caused by the Concomitant Effect of Variants in OPN1LW/OPN1MW and GPR143 Genes
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.
33. Focal electroretinograms and fundus appearance in nonexudative age-related macular degeneration: Quantitative relationship between retinal morphology and function
34. CRB1 -Related Cystic Maculopathy in Twins Conceived Through Heterologous Fertilization With Variant-Carrying Oocytes
35. 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?
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
41. The first and second harmonics of the macular flicker electroretinogram: Differential effects of retinal diseases
42. A fast visual evoked potential method for functional assessment and follow-up of childhood optic gliomas
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
49. The fundamental and second harmonic of the photopic flicker electroretinogram: temporal frequency-dependent abnormalities in retinitis pigmentosa
50. Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations
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