Source: Wikipedia. Pages: 98. Chapters: Achromatopsia, Akinetopsia, Amblyopia, Anopsia, Apperceptive agnosia, Associative visual agnosia, Asthenopia, Binasal hemianopsia, Binocular dysphoria, Bitemporal hemianopsia, Blindness, Chiasmal syndrome, Color blindness, Conjugate gaze palsy, Dichromacy, Diplopia, Entomopia, Eyeborg, Hemeralopia, Homonymous hemianopsia, Horizontal gaze palsy, Leber's congenital amaurosis, Low vision, Low vision assessment, Macular degeneration, Metamorphopsia, Monochromacy, Nyctalopia, Oguchi disease, Optic disc pallor, Photophobia, Prosopagnosia, Prosopamnesia, Quadrantanopia, Scintillating scotoma, Scleral reinforcement surgery, Toxic amblyopia, Vision disorder. Excerpt: 126 article summaries including: Associative visual agnosia resulting from a disconnection between intact visual memory and semantic systems. Unilateral Horizontal Gaze Palsy. Bilateral Horizontal Gaze Palsy. Congenital Horizontal Gaze Palsy. Unilateral Horizontal Gaze Palsy. Yellowish flecks in Leber's congenital amaurosis. Leber's congenital amaurosis--a new syndrome with a cardiomyopathy. A gene for Leber's congenital amaurosis maps to chromosome 17p. Leber's congenital amaurosis--a new syndrome with a cardiomyopathy. Pituitary Apoplexy without Optic Disc Pallor: A Case Report. Unique Cause of Complete Horizontal Gaze Palsy. Identification of differentially regulated proteins in a patient with Leber's Congenital Amaurosis – a proteomic study. Effect of gene therapy on visual function in Leber's congenital amaurosis. Progression of phenotype in Leber's congenital amaurosis with a mutation at the LCA5 locus. Progession of phenotype in Leber's congenital amaurosis with a mutation at the LCA5 locus. An unusual retinal vascular morphology in connection with a novel AIPL1 mutation in Leber's congenital amaurosis. Gene Therapy for Leber's Congenital Amaurosis is Safe and Effective Through 15 Years After Vector Administration. Bax-Induced Apoptosis in Leber's Congenital Amaurosis: A Dual Role in Rod and Cone Degeneration. Progession of phenotype in Leber’s congenital amaurosis with a mutation at the LCA5 locus. Bax-Induced Apoptosis in Leber's Congenital Amaurosis: A Dual Role in Rod and Cone Degeneration. Identification of differentially regulated proteins in a patient with Leber's Congenital Amaurosis – a proteomic study. The optic disc in glaucoma, III: diffuse optic disc pallor with raised intraocular pressure. Congenital horizontal gaze palsy and kyphoscoliosis in two brothers. Juvenile Gaucher's disease with horizontal gaze palsy in three siblings. Congenital horizontal gaze palsy and kyphoscoliosis in two brothers. AIPL1, a protein implicated in Leber's congenital amaurosis, interacts with and aids in processing of farnesylated proteins. Triggering of Bcl-2-related pathway is associated with apoptosis of photoreceptors in Rpe65(-/-) mouse model of Leber's Congenital Amaurosis. Bitemporal Hemianopsia, Recurrent Meningitis, and Presumed Empty Sella. Macular degeneration. Synergistic convergence and split pons in horizontal gaze palsy and progressive scoliosis in two sisters. Horizontal gaze palsy with progressive scoliosis can result from compound heterozygous mutations in ROBO3. Synergistic convergence and split pons in horizontal gaze palsy and progressive scoliosis in two sisters. Limited proteolysis differentia.

Hersteller:
BoD - Books on Demand
info@bod.de
In de Tarpen 42
DE 22848 Norderstedt