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	3661.	[Risk factors in the results of the colour vision test Roth 28-hue (E) desaturated in glaucoma patients]. [electronic resource] by Jass, C M Böhringer, D Erb, C Jordan, J F Producer: 20140829 In: Klinische Monatsblatter fur Augenheilkunde vol. 230 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3662.	A woman with bilateral maculopathy and acquired vitamin B12 deficiency. [electronic resource] by Doan, T Chao, J R Producer: 20141215 In: Eye (London, England) vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3663.	Color vision study to assess the impaired retina-brain cortex pathway in type 2 diabetes: a pilot study in Calabria (Southern Italy). [electronic resource] by Piro, Anna Tagarelli, Antonio Lagonia, Paolo Nicoletti, Giuseppe Quattrone, Aldo Producer: 20200212 In: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3664.	Two systems for colour-naming defects: verbal disconnection vs colour imagery disorder. [electronic resource] by De Vreese, L P Producer: 19910522 In: Neuropsychologia vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3665.	Cone dystrophies: clinical and electrophysiological findings. [electronic resource] by Kellner, U Kleine-Hartlage, P Foerster, M H Producer: 19930211 In: German journal of ophthalmology vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	3666.	Solar retinopathy and foveomacular retinitis. [electronic resource] by Wergeland, F L Brenner, E H Producer: 19751011 In: Annals of ophthalmology vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	3667.	X linked progressive cone dystrophy. Localisation of the gene locus to Xp21-p11.1 by linkage analysis. [electronic resource] by Meire, F M Bergen, A A De Rouck, A Leys, M Delleman, J W Producer: 19940412 In: The British journal of ophthalmology vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3668.	Toxic optic neuropathy after concomitant use of melatonin, zoloft, and a high-protein diet. [electronic resource] by Lehman, N L Johnson, L N Producer: 20000105 In: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	3669.	Analysis of red/green color discrimination in subjects with a single X-linked photopigment gene. [electronic resource] by Crognale, M A Teller, D Y Yamaguchi, T Motulsky, A G Deeb, S S Producer: 19990615 In: Vision research vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3670.	TRAFFIC ACCIDENTS--EPIDEMIOLOGY AND MEDICAL ASPECTS OF PREVENTION. [electronic resource] by WILLIAMS, N Producer: 19961201 In: Canadian Medical Association journal vol. 90 Availability: No items available. Save to lists Add to cart (remove)
	3671.	Clinical heterogeneity between two Japanese siblings with congenital achromatopsia. [electronic resource] by Hayashi, Takaaki Kozaki, Kenichi Kitahara, Kenji Kubo, Akiko Nishio, Yoshiteru Omoto, Satoshi Nakamura, Yosuke Watanabe, Akira Toda, Kazushige Ueoka, Yasuo Producer: 20050111 In: Visual neuroscience vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3672.	Achromatopsia caused by novel mutations in both CNGA3 and CNGB3. [electronic resource] by Johnson, S Michaelides, M Aligianis, I A Ainsworth, J R Mollon, J D Maher, E R Moore, A T Hunt, D M Producer: 20040223 In: Journal of medical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3673.	A novel mutation in the short-wavelength-sensitive cone pigment gene associated with a tritan color vision defect. [electronic resource] by Gunther, Karen L Neitz, Jay Neitz, Maureen Producer: 20061018 In: Visual neuroscience vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3674.	Substitution of isoleucine for threonine at position 190 of S-opsin causes S-cone-function abnormalities. [electronic resource] by Baraas, Rigmor C Hagen, Lene A Dees, Elise W Neitz, Maureen Producer: 20130507 In: Vision research vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3675.	The use of a system analysis approach to electrodiagnostic (ERG and VEP) assessment. [electronic resource] by Spekreijse, H Apkarian, P Producer: 19860630 In: Vision research vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3676.	Vision characteristics of deaf students. [electronic resource] by Pollard, G Neumaier, R Producer: 19750206 In: American journal of optometry and physiological optics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3677.	[Harmful effects of common drugs on the visual apparatus. The oligo-elements and chelating agents. A. The oligo-elements]. [electronic resource] by Le Jeune, J R Producer: 19720921 In: Bulletin de la Societe belge d'ophtalmologie vol. 160 Availability: No items available. Save to lists Add to cart (remove)
	3678.	Leber hereditary optic neuropathy associated with antiretroviral therapy for human immunodeficiency virus infection. [electronic resource] by Shaikh, S Ta, C Basham, A A Mansour, S Producer: 20010308 In: American journal of ophthalmology vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3679.	Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) families. [electronic resource] by Ebenezer, Neil D Michaelides, Michel Jenkins, Sharon A Audo, Isabelle Webster, Andrew R Cheetham, Michael E Stockman, Andrew Maher, Eamonn R Ainsworth, John R Yates, John R Bradshaw, Keith Holder, Graham E Moore, Anthony T Hardcastle, Alison J Producer: 20050721 In: Investigative ophthalmology & visual science vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3680.	Progressive cone dystrophy with deutan genotype and phenotype. [electronic resource] by Scholl, Hendrik P N Kremers, Jan Besch, Dorothea Zrenner, Eberhart Jägle, Herbert Producer: 20070510 In: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie vol. 244 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 4032 results.