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Nippon Ganka Gakkai zasshi, ISSN 0029-0203, 05/2013, Volume 117, Issue 5, pp. 415 - 417
Journal Article
Japanese Journal of Ophthalmology, ISSN 0021-5155, 05/2017, Volume 61, Issue 3, pp. 237 - 244
Journal Article
Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 9/2016, Volume 254, Issue 9, pp. 1859 - 1860
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s00417-016-3380-4 
Medicine & Public Health | Ophthalmology | OPHTHALMOLOGY | POCKET | SEROUS MACULAR DETACHMENT | VITREOUS FINDINGS | COHERENCE TOMOGRAPHY | NERVE PITS | Retinal Diseases | Eye Abnormalities | Optic Nerve Diseases | Optic Disk | Traction | Humans
Journal Article
British Journal of Ophthalmology, ISSN 0007-1161, 05/2016, Volume 100, Issue 5, pp. 611 - 615
PurposeTo identify areas of consensus and disagreement in the management of paediatric cataract using a modified Delphi approach among individuals recognised... 
Cataract - complications | Delphi Technique | Cataract Extraction | Humans | Adolescent | Child, Preschool | Infant | Practice Patterns, Physicians | Evidence-Based Medicine | Child | Consensus | Usage | Cataract | Care and treatment | Research | Vision disorders in children | Delphi technique | Cataracts | Hospitals | Experts | Surgery | Questionnaires | Eye surgery | Delphi method
Journal Article
Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 11/2016, Volume 254, Issue 11, pp. 2197 - 2201
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 16757 - 13
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 8279 - 11
Leber congenital amaurosis (LCA) is a genetically and clinically heterogeneous disease, and represents the most severe form of inherited retinal dystrophy... 
CLINICAL DEFINITION | REFINEMENT | NMNAT1 | ONSET RETINAL DYSTROPHY | RPGRIP1 GENE | MULTIDISCIPLINARY SCIENCES | DISEASE | RECESSIVE RETINITIS-PIGMENTOSA | GENETIC-HETEROGENEITY | COHORT | MUTATIONS | Polymerase chain reaction | Copy number | Blindness | Retinal degeneration | Retina | Diagnosis | Mutation | Dystrophy
Journal Article