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1. This actually looks like that: Proto-BagNets for local and global interpretability-by-design

2. Generating Realistic Counterfactuals for Retinal Fundus and OCT Images using Diffusion Models

6. Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment

10. A morphometric analysis of the retinal arterioles with adaptive optics imaging in RPE65‐associated retinal dystrophy after treatment with voretigene neparvovec

13. A morphometric analysis of the retinal arterioles with adaptive optics imaging in RPE65‐associated retinal dystrophy after treatment with voretigene neparvovec.

16. Rod and Cone Function Measured Objectively by Chromatic Pupil Campimetry Show a Different Preservation Between Distinct Genotypes in Retinitis Pigmentosa

19. CHANGES IN RETINAL SENSITIVITY AFTER GENE THERAPY IN CHOROIDEREMIA

23. Clinical Phenotype of PDE6B-Associated Retinitis Pigmentosa

24. Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment

25. Three-year results of phase I retinal gene therapy trial for CNGA3-mutated achromatopsia: results of a non randomised controlled trial.

26. Chromatic Pupil Campimetry Reveals Functional Defects in Exudative Age-Related Macular Degeneration with Differences Related to Disease Activity

27. Safety and Vision Outcomes of Subretinal Gene Therapy Targeting Cone Photoreceptors in Achromatopsia

28. Three-year results of phase I retinal gene therapy trial for CNGA3-mutated achromatopsia: results of a non randomised controlled trial

30. Clinical Protocols for the Evaluation of Rod Function

31. Genetic architecture of inherited retinal degeneration in Germany: A large cohort study from a single diagnostic center over a 9‐year period

32. Second opinion in retinal imaging

33. Clinical Protocols for the Evaluation of Rod Function.

35. Chromatic Full-Field Stimulus Threshold and Pupillography as Functional Markers for Late-Stage, Early-Onset Retinitis Pigmentosa Caused by CRB1 Mutations

37. Efficacy and Safety of Retinal Gene Therapy Using Adeno-Associated Virus Vector for Patients With Choroideremia

38. Chromatic Full-Field Stimulus Threshold and Pupillography as Functional Markers for Late-Stage, Early-Onset Retinitis Pigmentosa Caused by CRB1 Mutations

39. Development and validation of novel clinical endpoints in intermediate age-related macular degeneration in MACUSTAR

40. Changes in microchip position after implantation of a subretinal vision prosthesis in humans

41. Clinical Phenotype and Course of PDE6A-Associated Retinitis Pigmentosa Disease, Characterized in Preparation for a Gene Supplementation Trial.

42. Olfactory dysfunction in patients with CNGB1-related retinitis pigmentosa

43. Optical Coherence Tomography in Patients With the Subretinal Implant Retina Implant Alpha IMS

45. MACUSTAR: Entwicklung und klinische Validierung von funktionellen, strukturellen und patientenberichteten Endpunkten bei intermediärer altersabhängiger Makuladegeneration.

46. Retinal Capillary Network and Foveal Avascular Zone in Eyes with Vein Occlusion and Fellow Eyes Analyzed With Optical Coherence Tomography Angiography

47. Retinal Capillary Network and Foveal Avascular Zone in Eyes with Vein Occlusion and Fellow Eyes Analyzed With Optical Coherence Tomography Angiography

50. Ophthalmic features of cone‐rod dystrophy caused by pathogenic variants in the ALMS1 gene.

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