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Title: TYPICAL TOTAL MONOCHROMACY - A HISTOLOGICAL AND PSYCHOPHYSICAL STUDY
Author(s): FALLS, HF
Source: ARCHIVES OF OPHTHALMOLOGY Volume: 74 Issue: 5 Pages: 610-& Published: 1965
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1. Title: In vivo imaging of the photoreceptor mosaic of a rod monochromat
Author(s): Carroll J, Choi SS, Williams DR
Source: VISION RESEARCH   Volume: 48   Issue: 26   Special Issue: Sp. Iss. SI   Pages: 2564-2568   Published: NOV 2008
2. Title: Leber congenital amaurosis: Genes, proteins and disease mechanisms
Author(s): den Hollander AI, Roepman R, Koenekoop RK, et al.
Source: PROGRESS IN RETINAL AND EYE RESEARCH   Volume: 27   Issue: 4   Pages: 391-419   Published: JUL 2008
3. Title: CNGB3 achromatopsia with progressive loss of residual cone function and impaired rod-mediated function
Author(s): Khan NW, Wissinger B, Kohl S, et al.
Source: INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE   Volume: 48   Issue: 8   Pages: 3864-3871   Published: AUG 2007
4. Title: Optical coherence tomography of the macula in congenital achromatopsia
Author(s): Varsanyi B, Somfai GM, Lesch B, et al.
Source: INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE   Volume: 48   Issue: 5   Pages: 2249-2253   Published: MAY 2007
5. Title: Quantitative analysis of OCT characteristics in patients with achromatopsia and blue-cone monochromatism
Author(s): Barthelmes D, Sutter FK, Kurz-Levin MM, et al.
Source: INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE   Volume: 47   Issue: 3   Pages: 1161-1166   Published: MAR 2006
6. Title: Clinical and genetic features of Hungarian achromatopsia patients
Author(s): Varsanyi B, Wissinger B, Kohl S, et al.
Source: MOLECULAR VISION   Volume: 11   Issue: 118-20   Published: NOV 17 2005
7. Title: Impaired opsin targeting and cone photoreceptor migration in the retina of mice lacking the cyclic nucleotide-gated channel CNGA3
Author(s): Michalakis S, Geiger H, Haverkamp S, et al.
Source: INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE   Volume: 46   Issue: 4   Pages: 1516-1524   Published: APR 2005
8. Title: Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases
Author(s): Nishiguchi KM, Sandberg MA, Gorji N, et al.
Source: HUMAN MUTATION   Volume: 25   Issue: 3   Pages: 248-258   Published: 2005
9. Title: CNGA3 mutations in hereditary cone photoreceptor disorders
Author(s): Wissinger B, Gamer D, Jagle H, et al.
Source: AMERICAN JOURNAL OF HUMAN GENETICS   Volume: 69   Issue: 4   Pages: 722-737   Published: OCT 2001
10. Title: Rod pathways: the importance of seeing nothing
Author(s): Sharpe LT, Stockman A
Source: TRENDS IN NEUROSCIENCES   Volume: 22   Issue: 11   Pages: 497-504   Published: NOV 1999