GJ Ben Simon, FA Abraham, S Melamed - British Journal of Ophthalmology, 2004 - bjo.bmj.com Methods: 27 patients with PA were examined. All underwent a full ophthalmic
examination which included Snellen visual acuity and ophthalmoscopy. Colour
vision examination was performed with Ishihara pseudoisochromatic plates ... Cited by 4 - Related articles - BL Direct - All 9 versions
PS O'CONNOR, TJ TREDCI… - Journal of Neuro-Ophthalmology, 1982 - journals.lww.com Six cases of classic achromatopsia arc presented. The methods of practical
clinical diagnosis are discussed, including paradoxical pupillary constriction
in darkness, the easily performed Sloan achromatopsia test, and ... Cited by 5 - Related articles - All 2 versions
G Fonda, H Thomas - Archives of Ophthalmology, 1974 - archopht.highwire.org The principal characteristics of achro¬ matopsia are complete color blindness,
subnormal vision, and severe photo¬ phobia. It is usually a recessive
hereditary trait. The visual acuity of 80% of the pa¬ tients studied ... Cited by 1 - Related articles - All 3 versions
EM Scheiner, OD - Clinical Eye and Vision Care, 1999 - Elsevier Inherited macular dystrophies present with varying clinical signs. They possess
significant overlap with other inherited retinal dystrophies and with several
acquired retinal degenerations. A classification system for diagnostic ... Cited by 1 - Related articles - All 5 versions
G Ohmi, I Gottlob, SS Wizov, RD Reinecke - Binocular vision & strabismus quarterly, 1999 - ncbi.nlm.nih.gov PURPOSE: To elucidate the mechanism of paradoxical pupillary constriction to
darkness (PPCD) and the clinical characteristics facilitating this phenomenon.
METHODS: Six rod monochromats, three blue cone monochromats, with three ... Cited by 1 - Related articles - BL Direct
MM Schornack, WL Brown, DW Siemsen - Optometry-Journal of the American Optometric …, 2007 - Elsevier Achromatopsia is a congenital, autosomal recessively inherited condition in
which cones are either defective or absent. Complete achromatopsia results from
having only rods as functioning photoreceptors. Many people with ... Cited by 2 - Related articles - BL Direct - All 2 versions
[CITATION] Marx T, Giddings I, et al. Total colourblindness is caused by mutations in the gene …
M Li, JD Firth, EE Putnins - Journal of periodontal research, 2005 - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Cited by 3 - Related articles - All 4 versions
