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Results: 1-15 |
Results: 15
Some recent developments in evolutionary approaches to the study of human cognition and behavior
Authors: Downes, SM
Citation: Sm. Downes, Some recent developments in evolutionary approaches to the study of human cognition and behavior, BIOL PHILOS, 16(5), 2001, pp. 575-595
Polypoidal choroidal vasculopathy and central serous chorioretinopathy
Authors: Ahuja, RM Downes, SM Stanga, PE Koh, AHC Vingerling, JR Bird, AC
Citation: Rm. Ahuja et al., Polypoidal choroidal vasculopathy and central serous chorioretinopathy, OPHTHALMOL, 108(6), 2001, pp. 1009-1010
Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies
Authors: Payne, AM Morris, AG Downes, SM Johnson, S Bird, AC Moore, AT Bhattacharya, SS Hunt, DM
Citation: Am. Payne et al., Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies, J MED GENET, 38(9), 2001, pp. 611-614
Visual loss due to progressive multifocal leukoencephalopathy in a congenital immunodeficiency disorder
Authors: Downes, SM Black, GCM Hyman, N Simmonds, M Morris, J Barton, C
Citation: Sm. Downes et al., Visual loss due to progressive multifocal leukoencephalopathy in a congenital immunodeficiency disorder, ARCH OPHTH, 119(9), 2001, pp. 1376-1378
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1
Authors: Downes, SM Payne, AM Kelsell, RE Fitzke, FW Holder, GE Hunt, DM Moore, AT Bird, AC
Citation: Sm. Downes et al., Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1, ARCH OPHTH, 119(11), 2001, pp. 1667-1673
Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1
Authors: Downes, SM Holder, GE Fitzke, FW Payne, AM Warren, MJ Bhattacharya, SS Bird, AC
Citation: Sm. Downes et al., Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1, ARCH OPHTH, 119(1), 2001, pp. 96-105
Ophthalmologists' perspective
Authors: Downes, SM Chong, NHV Bird, AC
Citation: Sm. Downes et al., Ophthalmologists' perspective, METH MOL M, 47, 2001, pp. 251-305
Truth, selection and scientific inquiry
Authors: Downes, SM
Citation: Sm. Downes, Truth, selection and scientific inquiry, BIOL PHILOS, 15(3), 2000, pp. 425-442
Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclase
Authors: Gregory-Evans, K Kelsell, RE Gregory-Evans, CY Downes, SM Fitzke, FW Holder, GE Simunovic, M Mollon, JD Taylor, R Hunt, DM Bird, AC Moore, AT
Citation: K. Gregory-evans et al., Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclase, OPHTHALMOL, 107(1), 2000, pp. 55-61
Science.
Authors: Downes, SM
Citation: Sm. Downes, Science., PHILOS S SC, 30(1), 2000, pp. 140-145
Familial cavernous hemangioma - An expanding ocular spectrum
Authors: Sarraf, D Payne, AM Kitchen, ND Sehmi, KS Downes, SM Bird, AC
Citation: D. Sarraf et al., Familial cavernous hemangioma - An expanding ocular spectrum, ARCH OPHTH, 118(7), 2000, pp. 969-973
Can scientific development and children's cognitive development be the same process?
Authors: Downes, SM
Citation: Sm. Downes, Can scientific development and children's cognitive development be the same process?, PHILOS SCI, 66(4), 1999, pp. 565-578
Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies
Authors: Payne, AM Downes, SM Bessant, DAR Plant, C Moore, T Bird, AC Bhattacharya, SS
Citation: Am. Payne et al., Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies, J MED GENET, 36(9), 1999, pp. 691-693
Clinical features of codon 172 RDS macular dystrophy - Similar phenotype in 12 families
Authors: Downes, SM Fitzke, FW Holder, GE Payne, AM Bessant, DAR Bhattacharya, SS Bird, AC
Citation: Sm. Downes et al., Clinical features of codon 172 RDS macular dystrophy - Similar phenotype in 12 families, ARCH OPHTH, 117(10), 1999, pp. 1373-1383
Ontogeny, phylogeny, and scientific development
Authors: Downes, SM
Citation: Sm. Downes, Ontogeny, phylogeny, and scientific development, WHERE BIOLOGY MEETS PSYCHOLOGY, 1999, pp. 273-285
Risultati: 1-15 |