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	3901.	[Colour comparison tests in unilateral optic neuropathies]. [electronic resource] by Braun, F Wilhelm, H Producer: 20110425 In: Klinische Monatsblatter fur Augenheilkunde vol. 227 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3902.	CNGA3 achromatopsia-associated mutation potentiates the phosphoinositide sensitivity of cone photoreceptor CNG channels by altering intersubunit interactions. [electronic resource] by Dai, Gucan Varnum, Michael D Producer: 20130917 In: American journal of physiology. Cell physiology vol. 305 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3903.	The Clinical Phenotype of CNGA3-Related Achromatopsia: Pretreatment Characterization in Preparation of a Gene Replacement Therapy Trial. [electronic resource] by Zobor, Ditta Werner, Annette Stanzial, Franco Benedicenti, Francesco Rudolph, Günther Kellner, Ulrich Hamel, Christian Andréasson, Sten Zobor, Gergely Strasser, Torsten Wissinger, Bernd Kohl, Susanne Zrenner, Eberhart Producer: 20170621 In: Investigative ophthalmology & visual science vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3904.	Gene Augmentation Therapy Restores Retinal Function and Visual Behavior in a Sheep Model of CNGA3 Achromatopsia. [electronic resource] by Banin, Eyal Gootwine, Elisha Obolensky, Alexey Ezra-Elia, Raaya Ejzenberg, Ayala Zelinger, Lina Honig, Hen Rosov, Alexander Yamin, Esther Sharon, Dror Averbukh, Edward Hauswirth, William W Ofri, Ron Producer: 20160524 In: Molecular therapy : the journal of the American Society of Gene Therapy vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3905.	Genetics and physiology of colour vision. II. [electronic resource] by Waaler, G H Producer: 19750127 In: Acta ophthalmologica. Supplementum no. 124 Availability: No items available. Save to lists Add to cart (remove)
	3906.	Newer insights into the role and modifications of olfaction in man through clinical studies. [electronic resource] by Schneider, R A Producer: 19750115 In: Annals of the New York Academy of Sciences vol. 237 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3907.	Canine CNGB3 mutations establish cone degeneration as orthologous to the human achromatopsia locus ACHM3. [electronic resource] by Sidjanin, Duska J Lowe, Jennifer K McElwee, John L Milne, Bruce S Phippen, Taryn M Sargan, David R Aguirre, Gustavo D Acland, Gregory M Ostrander, Elaine A Producer: 20030205 In: Human molecular genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3908.	Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2. [electronic resource] by Hope, Carolyn I Sharp, Dianne M Hemara-Wahanui, Ariana Sissingh, Jennifer I Lundon, Patricia Mitchell, Ed A Maw, Marion A Clover, Gillian M Producer: 20050607 In: Clinical & experimental ophthalmology vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3909.	Mercury toxicity in the Amazon: contrast sensitivity and color discrimination of subjects exposed to mercury. [electronic resource] by Rodrigues, A R Souza, C R B Braga, A M Rodrigues, P S S Silveira, A T Damin, E T B Côrtes, M I T Castro, A J O Mello, G A Vieira, J L F Pinheiro, M C N Ventura, D F Silveira, L C L Producer: 20080131 In: Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3910.	Decreased retinal nerve fibre layer thickness detected by optical coherence tomography in patients with ethambutol-induced optic neuropathy. [electronic resource] by Chai, Samantha J Foroozan, Rod Producer: 20070730 In: The British journal of ophthalmology vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3911.	Visual processing in adolescents born extremely low birth weight and/or extremely preterm. [electronic resource] by Molloy, Carly S Wilson-Ching, Michelle Anderson, Vicki A Roberts, Gehan Anderson, Peter J Doyle, Lex W Producer: 20131030 In: Pediatrics vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3912.	An A-71C substitution in a green gene at the second position in the red/green visual-pigment gene array is associated with deutan color-vision deficiency. [electronic resource] by Ueyama, Hisao Li, Yao-Hua Fu, Gui-Lian Lertrit, Patcharee Atchaneeyasakul, La-ongsri Oda, Sanae Tanabe, Shoko Nishida, Yasuhiro Yamade, Shinichi Ohkubo, Iwao Producer: 20030421 In: Proceedings of the National Academy of Sciences of the United States of America vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3913.	Occupational styrene exposure, colour vision and contrast sensitivity: a cohort study with repeated measurements. [electronic resource] by Seeber, Andreas Bruckner, Thomas Triebig, Gerhard Producer: 20090716 In: International archives of occupational and environmental health vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3914.	Mutation in the gene GUCA1A, encoding guanylate cyclase-activating protein 1, causes cone, cone-rod, and macular dystrophy. [electronic resource] by Michaelides, Michel Wilkie, Susan E Jenkins, Sharon Holder, Graham E Hunt, David M Moore, Anthony T Webster, Andrew R Producer: 20050816 In: Ophthalmology vol. 112 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3915.	Visual electrophysiological screening in diagnosing infants with congenital nystagmus. [electronic resource] by Brecelj, Jelka Stirn-Kranjc, Branka Producer: 20040322 In: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology vol. 115 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3916.	G-6-PD Worcester. A new variant, associated with X-linked optic atrophy. [electronic resource] by Snyder, L M Necheles, T F Reddy, W J Producer: 19701005 In: The American journal of medicine vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3917.	Novel KCNV2 mutations in cone dystrophy with supernormal rod electroretinogram. [electronic resource] by Ben Salah, Safouane Kamei, Satomi Sénéćhal, Audrey Lopez, Séverine Bazalgette, Christian Bazalgette, Cécile Eliaou, Claudie Malrieu Zanlonghi, Xavier Hamel, Christian P Producer: 20080624 In: American journal of ophthalmology vol. 145 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3918.	Association between retinal nerve fiber layer thickness and abnormalities of vision in people with human immunodeficiency virus infection. [electronic resource] by Kalyani, Partho S Holland, Gary N Fawzi, Amani A Arantes, Tiago E F Yu, Fei Sadun, Alfredo A Producer: 20120509 In: American journal of ophthalmology vol. 153 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3919.	Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophy. [electronic resource] by Shaikh, Rehan S Reuter, Peggy Sisk, Robert A Kausar, Tasleem Shahzad, Mohsin Maqsood, Muhammad I Yousif, Ateeq Ali, Muhammad Riazuddin, Saima Wissinger, Bernd Ahmed, Zubair M Producer: 20151215 In: European journal of human genetics : EJHG vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3920.	Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24. [electronic resource] by Khaliq, S Hameed, A Ismail, M Anwar, K Leroy, B P Mehdi, S Q Payne, A M Bhattacharya, S S Producer: 20001114 In: Investigative ophthalmology & visual science vol. 41 Availability: No items available. Save to lists Add to cart (remove)

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