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1994, ISBN 9780521451093, x, 380
The book is a summary and interpretation of the research literature on infants and children with visual impairments. It concludes that many aspects of... 
in infancy & childhood | Development | Children with disabilities | Blind children | Blindness
Book
1985, Cognitive science series, ISBN 0674510259, Volume 8, xi, 250
Book
Childhood blindness in Cali, Colombia, 12/2005
INTRODUCTION: Retinopathy of prematurity is the major cause of blindness (33.8%) in children who study at the "Instituto para niños ciegos y sordos del Valle... 
Ceguera prevenible en niños | Retinopathy of prematurity | Retinopatía de la prematuridad | Toxoplasmosis | Ocular toxoplasmosis | Avoidable childhood blindness
Journal
1992, ISBN 9789241561518, vi, 50 p., [8] p. plates
Book
1984, 2nd ed. rev. --, ISBN 9780891281238, 377
Book
1977, ISBN 9780891280743, x, 308
Book
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2012, Volume 109, Issue 6, pp. 2132 - 2137
Hereditary retinal blindness is caused by mutations in genes expressed in photoreceptors or retinal pigment epithelium. Gene therapy in mouse and dog models of... 
Eyes | Disease vectors | Disease models | Canines | Retinitis pigmentosa | Photoreceptors | Retina | Gene therapy | Retinal diseases | Genetic mutation | Retinal degeneration | MUTATION ANALYSIS | retinal degeneration | LEBER CONGENITAL AMAUROSIS | CHILDHOOD BLINDNESS | CANINE MODEL | retina | CONE VISION | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | RPGR EXON ORF15 | GTPASE REGULATOR RPGR | DISEASE EXPRESSION | Genetic Therapy | Retinal Bipolar Cells - pathology | Humans | Retinitis Pigmentosa - genetics | Genotype | Eye Proteins - therapeutic use | Mutation - genetics | Open Reading Frames - genetics | Blindness - genetics | Protein Transport | Phenotype | Animals | Retinitis Pigmentosa - therapy | Dogs | Opsins - metabolism | Genetic Diseases, X-Linked - genetics | Mice | Blindness - therapy | Eye Proteins - genetics | Photoreceptor Cells, Vertebrate - pathology | Genetic Diseases, X-Linked - therapy | Care and treatment | Blindness | Physiological aspects | Genetic aspects | Research | Health aspects | Proteins | Mutation | Gene expression | Animal models | Translation | Preservation | X chromosome | Clinical trials | Rod outer segment membranes | Nuclei | Promoters | interphotoreceptor retinoid-binding protein | Cones | Bipolar cells | retinal pigment epithelium | Guanosinetriphosphatase | Index Medicus | Biological Sciences
Journal Article
Journal Article
Human Gene Therapy, ISSN 1043-0342, 10/2008, Volume 19, Issue 10, pp. 979 - 990
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 05/2008, Volume 358, Issue 21, pp. 2240 - 2248
Journal Article
Nature, ISSN 0028-0836, 10/2015, Volume 526, Issue 7574, pp. 487 - 488
  And on 10 October at the Retina Society annual scientific meeting in Paris, a biotechnology company presented encouraging data from a trial in humans. The...