Ocular physiology

References

• Mellerio J. Bioengineering and the Eye. Biomedical Engineering 1972; 7: 518–526
   PubMedGoogle Scholar
• Fisher R. F. The elastic constants of the human lens. Journal of Physiology 1971; 212: 147–180
   PubMed Web of Science ®Google Scholar
• Fisher R. F. The force of contraction of the human ciliary muscle during accommodation. Journal of Physiology 1977; 270: 51–74
   PubMed Web of Science ®Google Scholar
• Emsley H. “Visual Optics”, vol.1 and vol.2. Hatton Press, London 1952/3
   Google Scholar
• Davson H. “The Eye”, 2nd edn., volumes 1, 2A, 2B, 3 & 4. Academic Press, London 1969
   Google Scholar
• Marshall J., Grindle J. Fine structure of the cornea and its development. Transactions of the Ophthalmological Society of the U.K. 1979
   Google Scholar
• Farrell R. A., McCally R. L. On corneal transparency and its loss with swelling. Journal of the Optical Society of America 1976; 66: 342–345
   PubMed Web of Science ®Google Scholar
• Benedek C. B. Theory of the transparency of the eye. Applied Optics 1971; 10: 459–473
   PubMed Web of Science ®Google Scholar
• Cox J. L., Farrell R. A., Hart R. W., Langham M. E. Transparency of the mammalian cornea. Journal of Physiology 1970; 210: 601–626
   PubMed Web of Science ®Google Scholar
• Olson L. E., Marshall J., Rice N. S. C., Andrews R. Effects of ultrasound on the corneal endothelium. II Endothelial repair process. British Journal of Ophthalmology 1978; 62: 145–154
   PubMed Web of Science ®Google Scholar
• Mellerio J., Palmer D. A. Entoptic halos. Vision Research 1970; 10: 595–599
   PubMedGoogle Scholar
• Mellerio J., Palmer D. A. Entoptic halos and glare. Vision Research 1972; 12: 141–143
   PubMedGoogle Scholar
• Duke-Elder W. S. “System of Ophthalmology”. Volumes 11 and 14. Henry Kimpton, London 1969
   Google Scholar
• van Heynigen R. Assay of fluorescent glucosides in the human lens. Experimental Eye Research 1973; 15: 121–126
   PubMedGoogle Scholar
• Cooper G. F., Robson J. G. The yellow colour of the lens of man and other primates. Journal of Physiology 1969; 203: 411–417
   PubMed Web of Science ®Google Scholar
• Zigman S., Groff J., Yulo T., Griess G. Light extinction and protein in the lens. Experimental Eye Research 1976; 23: 555–567
   PubMed Web of Science ®Google Scholar
• Zigman S., Griess G., Yulo T., Schultz J. Ocular protein alterations by near U.V. light. Experimental Eye Research 1973; 15: 255–264
   PubMed Web of Science ®Google Scholar
• Said F. S., Weale R. A. Variation with age of the spectral transmissivity of the living human crystalline lens. Gerontologia 1959; 3: 213–231
   PubMedGoogle Scholar
• Mellerio J. Light absorption and scatter in the human lens. Vision Research 1971; 11: 129–141
   PubMed Web of Science ®Google Scholar
• Mellerio J. In preparation
   Google Scholar
• McNeill Alexander R. “Size and shape” Studies in Biology number 29. E. Arnold, London 1971
   Google Scholar
• Hill A. V. “Trails and Trials in Physiology”. E. Arnold, London 1965
   Google Scholar
• Cioli S. Passive and active transport in choroidal and retinal capillaries of various non-electrolyte substances in normal rats. Transactions of the Ophthalmological Society of the U.K. 1977; 97: 568–572
   PubMedGoogle Scholar
• Fisher R. F., Carpenter R. G., Wheeler C. Assessment of established cases of chronic simple glaucoma. British Journal of Ophthalmology 1970; 54: 217–228
   PubMedGoogle Scholar
• Bill A., Svedbergh B. Scanning E.M. studies of the trabecular meshwork and the canal of Schlemm etc. Acta Ophthalmologia 1972; 50: 295–320
   PubMed Web of Science ®Google Scholar
• Grierson L., Lee W. R., Moseley H., Abraham S. Trabecular wall of Schlemm's canal: a study of the effects of pilocarpine etc. British Journal of Ophthalmology 1979; 63: 9–16
   PubMedGoogle Scholar
• Grierson L., Lee W. R., Abraham S. Distribution and significance of hyaluronidase-sensitive materials in the trabecular wall of Schlemm's canal. Transactions of the Ophthalmological Society of the U.K. 1977; 97: 739–745
   PubMedGoogle Scholar
• Fukui H. N., Merola L. O., Kinoshita J. H. A possible cataractogenic factor in the Nakano mouse lens. Experimental Eye Research 1978; 26: 477–485
   PubMed Web of Science ®Google Scholar
• Zimmerman T. J. An analysis of the “vascular hypothesis” concerning optic disc pathology in glaucoma. Annals of Ophthalmology 1979; 11: 67–69
   PubMedGoogle Scholar
• Davson H. “The Eye”, vol 2B, Chapter 5, p 368 et seq. 2nd Edn. Academic Press, London 1977
   Google Scholar
• Davson H. “The Eye”, vol 2B, Chapter 12, 2nd Edn. Academic Press, London 1977
   Google Scholar
• Bangham A. D., Dingle J. T., Lucy J. A. Studies on the mode of action of excess vitamin A. 9: Penetration of lipid monolayers & etc. Biochemical Journal 1964; 90: 133–140
   PubMedGoogle Scholar
• Bok D., Heller J. Transport of retinol from blood to retina, etc. Experimental Eye Research 1976; 22: 395–402
   PubMedGoogle Scholar
• Bridges C. D. B. Vitamin A and the role of the pigment epithelium during bleaching and regeneration of rhodopsin in the frog eye. Experimental Eye Research 1976; 22: 435–455
   PubMedGoogle Scholar
• Hagins W. A., Yoshikami S. A role for Ca++ in excitation of retinal rods and cones. Experimental Eye Research 1974; 18: 299–305
   PubMed Web of Science ®Google Scholar
• Hagins W. A., Yoshikami S. Intracellular transmission of visual excitation in photoreceptors: electrical effects of chelating agents introduced into rods by vesicle fusion. “Vertebrate Photoreception”, H. B. Barlow, P. Fatt. Academic Press, London 1977
   Google Scholar
• Farber D. B., Brown B. M., Lolley R. N. Cyclic G M P proposed role in visual cell function. Vision Research 1978; 18: 497–499
   PubMed Web of Science ®Google Scholar
• Liebman P. A., Pugh E. N. The control of phosphodiesterase in rod disc membranes: kinetics, possible mechanisms and significance for vision. Vision Research 1979; 19: 375–380
   PubMed Web of Science ®Google Scholar
• Young R. W. Visual cells and the concept of renewal. Investigative Ophthalmology 1976; 15: 700–725
   Google Scholar
• Lavail M. M. Rod outer segment disc shedding in rat retina: relationship to cyclic lighting. Science 1976; 194: 1071–1074
   PubMed Web of Science ®Google Scholar
• Bassinger S., Hoffman R., Matthes M. Photoreceptor shedding is initiated by light in the frog retina. Science 1976; 194: 1074–1076
   PubMedGoogle Scholar
• Hollyfield J. G., Bassinger S. C. Photoreceptor shedding can be initiated within the eye. Nature 1978; 274: 794–796
   PubMed Web of Science ®Google Scholar
• Lavail M. M., Ward P. A. Studies on the hormonal control of circadian outer segment disc shedding in the rat retina. Invest. Ophthalm. Vis. Sci. 1978; 17: 1189–1193
   PubMedGoogle Scholar
• Marshall J., Personal communication
   Google Scholar
• Steinberg R. H., Wood I., Hogan M. J. Pigment epithelial ensheathment and phagocytosis of extrafoveal cones in the human retina. Philosophical Transactions of the Royal Society B. 1977; 277: 459–474
   PubMed Web of Science ®Google Scholar
• Ernst W., Noble B. Flicker in retinal dystrophy. 30th Annual Report. Institute of Ophthalmology, London 1978; 63
   Google Scholar
• Garland C. W. Sensory devices for the blind. Journal of Medical Engineering and Technology 1978; 2: 319–323
   Google Scholar
• Katz M. S., Stone W. L., Dratz E. A. Fluorescent pigment accumulation in retinal pigment epithelium of antioxidant-deficient rats. Investigative Ophthalmology 1978; 17: 1049–1058
   Google Scholar