Clinical study of a large family with autosomal dominant progressive cone degeneration.
暂无分享,去创建一个
[1] K. Gehrs,et al. Mapping of autosomal dominant cone degeneration to chromosome 17p. , 1996, American journal of ophthalmology.
[2] P. Humphries,et al. Autosomal dominant retinitis pigmentosa: a novel mutation in the rhodopsin gene in the original 3q linked family. , 1992, Human molecular genetics.
[3] J. Oosterhuis,et al. Late onset dominant cone dystrophy with early blue cone involvement. , 1992, Journal of medical genetics.
[4] H. Fledelius,et al. Deletion mapping of a retinal cone-rod dystrophy: assignment to 18q211. , 1991, American journal of medical genetics.
[5] M. Marmor,et al. Standard for Clinical Electroretinography: International Standardization Committee , 1989 .
[6] R. Carr,et al. Progressive peripheral cone dysfunction. , 1988, American journal of ophthalmology.
[7] D. Archer,et al. Retinal ultrastructural findings in cone degeneration. , 1988, American journal of ophthalmology.
[8] R. Weleber,et al. Normal α-L-Fucosidase and Other Lysosomal Enzyme Activities in Progressive Cone Dystrophy , 1988 .
[9] R. Carr,et al. Progressive cone dystrophy. , 1987, Transactions of the American Ophthalmological Society.
[10] M. Warburg,et al. Retinal cone dysfunction and mental retardation associated with a de novo balanced translocation 1;6(q44;q27). , 1986, Ophthalmic paediatrics and genetics.
[11] G. Fish,et al. A comparison of visual function tests in eyes with maculopathy. , 1986, Ophthalmology.
[12] G. Fishman,et al. Supernormal scotopic ERG in cone dystrophy. , 1984, The British journal of ophthalmology.
[13] P. Gouras,et al. Cone dystrophy, nyctalopia, and supernormal rod responses. A new retinal degeneration. , 1983, Archives of ophthalmology.
[14] M. Sandberg,et al. Foveal and parafoveal cone electroretinograms in juvenile macular degeneration , 1983 .
[15] G. Fishman,et al. Visual improvements with red-tinted glasses in a patient with cone dystrophy. , 1982, Archives of ophthalmology.
[16] S. Jacobson,et al. Foveal cone electroretinograms in retinitis pigmentosa and juvenile maular degeneration. , 1979, American journal of ophthalmology.
[17] R. Blach,et al. Bull's eye maculopathy with early cone degeneration. , 1977, The British journal of ophthalmology.
[18] J. Pearlman,et al. Cone dystrophy with dominant inheritance. , 1974, American journal of ophthalmology.
[19] R. Schachar,et al. Use of miotics in patients with cone degenerations. , 1973, American journal of ophthalmology.
[20] A. Deutman,et al. Dominant macular degenerations. The cone dystrophies. , 1972, American journal of ophthalmology.
[21] P. Gouras,et al. Progressive cone degeneration, dominantly inherited. , 1968, Archives of ophthalmology.
[22] H. Ripps,et al. CONE DYSFUNCTION SYNDROMES. , 1963, Archives of ophthalmology.
[23] K. N. Ogle,et al. Some physiologic considerations of hereditary mascular degeneration. , 1956, American journal of ophthalmology.