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Fig. 3.14  MfERG from patient with STGD involving the fovea. (a) fundus appearance, (b) raw waveforms, (c) six annular rings used for annular averages, (d) 3D representation showing

Acknowledgments  Supported by EY09076 (DGB) and EY05235 (EEB)

References

1. Dewar, J.: The physiologic action of light. Nature 15, 433–435 (1877)

2. Granit, R.: The components of the retinal action potential in mammals and their relation to the discharge in the optic nerve. J. Physiol. 77, 207–239 (1933)

3. Noell, W.K.: The origin of the electroretinogram. Am. J. Ophthalmol. 38, 78 (1954)

4. Brown, K.T., Wiesel, T.N.: Localization of origins of electroretinogram components by intraretinal recording in the intact cat eye. J. Physiol. 158, 257–280 (1961)

5. Brown, K.T.: The electroretinogram; its components and their origins. Vision Res. 8, 633 (1968)

6. Miller, R.F., Dowling, J.E.: Intracellular responses of the Muller (glial) cells of mudpuppy retina; their relation to b-wave of the electroretinogram. J. Neurophysiol. 33, 323 (1970)

profound­ loss in the fovea, and (e) responses and parameters from each annular ring

7. Marmor, M.F., et al.: Standard for clinical electroretinography. Arch. Ophthalmol. 107, 816–819 (1989)

8. Marmor, M.F., et al.: Standard for clinical electroretino­ graphy (2004 update). Doc. Ophthalmol. 108, 107–114 (2004)

9. Yonemura, D.: The oscillatory potential of the electroretino-

gram. Acta Soc. Ophthalmol. Jpn. 66, 1566–1584 (1963)

10.Speros, P., Price, J.: Oscillatory potentials. History, techniques and potential use in the evaluation of disturbances of retinal circulation. Surv. Ophthalmol. 25, 237 (1981)

11.MacKay, C.J., Gouras, P.: Light-adaptation augments the amplitude of the human cone ERG. Invest. Ophthalmol. Vis. Sci 26(suppl), 323 (1985)

12.Birch, D.G., et al.: Quantitative electroretinogram measures of phototransduction in cone and rod photoreceptors: normal aging, progression with disease, and test-retest variability. Arch. Ophthalmol. 120(8), 1045–1051 (2002)

13.Mactier, H., Dexter, J.D., Hewett, J.E.: The elec­ troretinogram in preterm infants. J. Pediatr. 113, 607–612 (1988)

14.Berezovsky, A., et al.: Standard full-field electroretinography in healthy preterm infants. Doc. Ophthalmol. 107, 243–249 (2003)

3  Electroretinographic Testing in Infants and Children

83

 

 

15.Birch, E.E., et al.: Retinal and cortical function of very low birth weight infants at 36 and 57 weeks postconception. Clin. Vis. Sci. 5(4), 363–373 (1990)

16.Mets, M., Smith, V.C.: Postnatal retinal development as measured by the electroretinogram in premature infants. Doc. Ophthalmol. 90, 111–127 (1995)

17.Birch, D.G., Anderson, J.L.: Standardized full-field electroretinography. Normal values and their variation with age. Arch. Ophthalmol. 110(11), 1571–1576 (1992)

18.Birch, D.G., et al.: Retinal development in very- low-birth-weight infants fed diets differing in omega-3 fatty acids. Invest. Ophthalmol. Vis. Sci. 33(8), 2365–2376 (1992)

19.Westall, C.A., Panton, C.M., Levin, A.V.: Time courses for maturation of electroretinogram responses from infancy to adulthood. Doc. Ophthalmol. 96, 355–379 (1999)

20.Fulton, A.B., Hansen, R.M., Westall, C.A.: Development of ERG responses: the ISCEV rod, maximal and cone responses in normal subjects. Doc. Ophthalmol. 107, 235–241 (2003)

21.Birch, D.G., et al.: The relationship between rod perimetric thresholds and full-field rod ERGs in retinitis pigmentosa. Invest. Ophthalmol. Vis. Sci. 28(6), 954–965 (1987)

22.Brown, A.M.: Development of visual sensitivity to light and color in human infants: a critical review. Vision Res. 30, 1159–1188 (1990)

23.Powers, M.K., Schneck, M.S., Teller, D.Y.: Spectral sensitivity of human infants at absolute threshold. Vision Res. 21, 1005–1016 (1981)

24.Hansen, R.M., Fulton, A.B., Harris, S.J.: Background adaptation in human infants. Vision Res. 26, 771–779 (1986)

25.Hamer, R.D., Schneck, M.E.: Spatial summation in darkadapted human infants. Vision Res. 24, 77–85 (1984)

26.Fulton, A.B., Hansen, R.M.: Background adaptation in human infants: analyses of b-wave responses. Doc. Ophthalmol. Proc. Ser. 31, 191–197 (1982)

27.Hood, D.C., Birch, D.G., Birch, E.E.: Use of models to improve hypothesis delineation: a study of infant electroretinography. In: Simons, K. (ed.) Early Visual Development, Normal and Abnormal, pp. 517–535. Oxford University Press, New York (1993)

28.Hood, D.C., Birch, D.G.: The a-wave of the human electroretinogram and rod receptor function. Invest. Ophthalmol. Vis. Sci. 31, 2070–2081 (1990)

29.Hood, D.C., Birch, D.G.: The relationship between models of receptor activity and the a-wave of the human ERG. Clin. Vis. Sci. 5, 293 (1990)

30.Breton, M.E., Montzka, D.P.: Empiric limits of rod photocurrent component underlying a-wave response in the electroretinogram. Doc. Ophthalmol. 79, 337–361 (1992)

31.Cideciyan, A.V., Jacobson, S.G.: Negative electroretinograms in retinitis pigmentosa. Invest. Ophthalmol. Vis. Sci. 34(12), 3253–3263 (1993)

32.Hood, D.C., Birch, D.G.: Light adaptation of human rod receptors: the leading edge of the human a-wave and models of rod receptor activity. Vision Res. 33(12), 1605–1618 (1993)

33.Baylor, D.A., Nunn, B.J., Schnapf, J.L.: The photocurrent, noise and spectral sensitivity of rods of the monkey Macaca fascicularis. J. Physiol. 357, 575–607 (1984)

34.Kraft, T.W., Schneeweis, D.M., Schnapf, J.L.: Visual transduction in human rod photoreceptors. J. Physiol. 464, 747– 765 (1993)

35.Hendrickson, A., Drucker, D.: The development of parafoveal and rod-ring human retina. Behav. Brain Res. 49, 21–31 (1992)

36.Packer, O., Hendrickson, A.E., Curcio, C.A.: Developmental redistribution of photoreceptors across the Macaca nemestrina (pigtail macaque) retina. J. Comp. Neurol. 298, 472–493 (1990)

37.Curcio, C.A., Hendrikson, A.: Organization and development of the primate photoreceptor mosaic. In: Osborn, N.N., Chader, G.J. (eds.) Progress in Retinal Research), pp. 90–120. Pergamon, Oxford (1991)

38.Fulton, A.B., et al.: The quantity of rhodopsin in young human eyes. Curr. Eye Res. 10, 977–982 (1991)

39.Dodge, J., et al.: Rhodopsin in immature rod outer segments. Invest. Ophthalmol. Vis. Sci. 37, 1951–1956 (1996)

40.Lee, R.H., Lieberman, B.S., Lolley, R.N.: Retinal accumulation of the phosducin/T and transducin complexes in developing normal mice and in mice and dogs with inherited retinal degeneration. Exp. Eye Res. 51, 325–333 (1990)

41.Berson, E.L., Gouras, P., Hoff, M.: Temporal aspects of the electroretinogram. Arch. Ophthalmol. 81(2), 207–214 (1969)

42.Berson, E.L., et al.: Rod and cone responses in sex-linked retinitis pigmentosa. Arch. Ophthalmol. 81(2), 215–225 (1969)

43.Berson, E.L., Kanters, L.: Cone and rod responses in a family with recessively inherited retinitis pigmentosa. Arch. Ophthalmol. 84(3), 288–297 (1970)

44.Berson, E.L., Gouras, P., Gunkel, R.D.: Rod responses in retinitispigmentosa,dominantlyinherited.Arch.Ophthalmol. 80(1), 58–67 (1968)

45.Berson, E.L.: Hereditary retinal diseases; classification with the full-field electroretinogram. In: Lawwill, T. (ed.) ERG, VER and Psychophysics (XIVth ISCERG Symposium, May 1976, Louisville, KY) W. Junk: The Hague (1977)

46.Berson,E.L.,Rosen,J.B.,Simonoff,E.A.:Electroretinographic testing as an aid in detection of carriers of X- chromosomelinked retinitis pigmentosa. Am. J. Ophthalmol. 87(4), 460–468 (1979)

47.Fishman, G.A., Cunha-Vaz, J.E.: Carriers of X-linked recessive retinitis pigmentosa: investigation by vitreous fluorophotometry. Int. Ophthalmol. 4(1–2), 37–44 (1981)

48.Berson, E.L., et al.: Natural course of retinitis pigmentosa over a three-year interval. Am. J. Ophthalmol. 99(3), 240– 251 (1985)

49.Birch, D.G., Anderson J.L. Yearly rates of rod and cone functional loss in retinitis pigmentosa and cone-rod degeneration. In: Vision Science and its Applications. OSA Technical Digest Series, vol. 3, pp. 334–337, Optical Society of America, Washington, D.C. (1993)

50.Kohl, S., et al.: Total colour blindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel. Nat. Genet. 19(3), 257– 259 (1998)

51.Wissinger, B., et al.: CNGA3 mutations in hereditary cone photoreceptor disorders. Am. J. Hum. Genet. 69(4), 722–737 (2001)

52.Sundin, O.H., et al.: Genetic basis of total colour blindness among the Pingelapese islanders. Nat. Genet. 25(3), 289–293 (2000)

53.Miyake, Y., et al.: Congenital stationary night blindness with negative electroretinogram. Arch. Ophthalmol. 104, 1013–1020 (1986)

84

D.G. Birch et al.

 

 

54.Miyake, Y., et al.: Characteristic ERG-flicker anomaly in incomplete congenital stationary night blindness. Invest. Ophthalmol. Vis. Sci. 28(11), 1816–1823 (1987)

55.Bech-Hansen, N.T., et al.: Mutations in the gene for a novel leucine-rich protein, nyctalopin, cause developmental reti- nal-circuitry abnormality in X-linked retinitis pigmentosa. Nat. Genet. 26, 319–323 (2000)

56.Bech-Hansen, N.T., et al.: Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness. Nat. Genet. 19(3), 264–7 (1998)

57.Milam, A.H., et al.: The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degeneration. Proc. Natl. Acad. Sci. USA. 99(1), 473–478 (2002)

58.Hood, D.C., et al.: Enhanced S cone syndrome: evidence for an abnormally large number of S cones. Vision Res. 35(10), 1473–1481 (1995)

59.Jacobson, S.G., et al.: SWS (blue) cone hypersensitivity in a newly identified retinal degeneration. Invest. Ophthalmol. Vis. Sci. 31, 827–838 (1990)

60.Marlhens, F., et al.: Mutations in RPE65 cause Leber’s congenital amaurosis. Nat. Genet. 17(2), 139–141 (1997)

61.Acland, G.M., et al.: Gene therapy restores vision in a canine model of childhood blindness. Nat. Genet. 28, 92–95 (2001)

62.Perrault, I., et al.: Retinal-specific guanylate cyclase gene mutations in Leber’s congenital amaurosis. Nat. Genet. 14(4), 461–464 (1996)

63.Freund, C.L., et al.: Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor. Cell 91(4), 543–553 (1997)

64.Sohocki, M.M., et al.: A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcriptionfactor gene. Am. J. Hum. Genet. 63(5), 1307–1315 (1998)

65.Sohocki, M.M., et al.: Mutations in a new photoreceptorpineal gene on 17p cause Leber congenital amaurosis. Nat. Genet. 24(1), 79–83 (2000)

66.Osterberg, G.: Topography of the layer of rods and cones in the human retina. Acta Ophthalmol. 13(Suppl 6), 11–96 (1935)

67.Sandberg, M.A., Ariel, M.: A hand-held, two-channel stim- ulator-ophthalmoscope. Arch. Ophthalmol. 95, 1881–1882 (1978)

68.Fish, G.E., Birch, D.G.: The focal electroretinogram in the clinical assessment of macular disease. Ophthalmology 96(1), 109–114 (1989)

69.Birch, D.G., Fish, G.E.: Focal cone electroretinograms: aging and macular disease. Doc. Ophthalmol. 69, 211–220 (1988)

70.Sutter, E.E.: The fast m-transform: a fast computation of cross-correlations with binary m-sequences. Soc. Ind. Appl. Math. 20, 686–694 (1991)

71.Hood, D.C., et al.: A comparison of the components of the multifocal and full-field ERGs. Vis. Neurosci. 14, 533–544 (1997)

72.Westall, C.A., et al.: The Hospital for Sick Children, Toronto. Longitudinal ERG study of children on vigabatrin. Doc. Ophthalmol. 104(2), 133–149 (2002)

73.Ponjavic, V., Andreasson, S.: Multifocal ERG and full-field ERG in patients on long-term vigabatrin medication. Doc. Ophthalmol. 102(1), 63–72 (2001)

74.Harding, G.F., et al.: Electro-oculography, electroretinography, visual evoked potentials, and multifocal electroretinography in patients with vigabatrin-attributed visual field constriction. Epilepsia 41(11), 1420–1431 (2000)