Kemp CM - Search Results

1

Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutation.

Moore AT, Fitzke FW, Kemp CM, Arden GB, Keen TJ, Inglehearn CF, Bhattacharya SS, Bird AC. Moore AT, et al. Among authors: kemp cm. Br J Ophthalmol. 1992 Aug;76(8):465-9. doi: 10.1136/bjo.76.8.465. Br J Ophthalmol. 1992. PMID: 1390527 Free PMC article.

2

Abnormal dark adaptation and rhodopsin kinetics in Sorsby's fundus dystrophy.

Steinmetz RL, Polkinghorne PC, Fitzke FW, Kemp CM, Bird AC. Steinmetz RL, et al. Among authors: kemp cm. Invest Ophthalmol Vis Sci. 1992 Apr;33(5):1633-6. Invest Ophthalmol Vis Sci. 1992. PMID: 1559761

3

Probing visual function with psychophysics and photochemistry.

Fitzke FW, Kemp CM. Fitzke FW, et al. Among authors: kemp cm. Eye (Lond). 1989;3 ( Pt 1):84-9. doi: 10.1038/eye.1989.12. Eye (Lond). 1989. PMID: 2591602

4

Abnormal rod dark adaptation in autosomal dominant retinitis pigmentosa with proline-23-histidine rhodopsin mutation.

Kemp CM, Jacobson SG, Roman AJ, Sung CH, Nathans J. Kemp CM, et al. Am J Ophthalmol. 1992 Feb 15;113(2):165-74. doi: 10.1016/s0002-9394(14)71529-6. Am J Ophthalmol. 1992. PMID: 1550184 Free article.

5

Two types of visual dysfunction in autosomal dominant retinitis pigmentosa.

Kemp CM, Jacobson SG, Faulkner DJ. Kemp CM, et al. Invest Ophthalmol Vis Sci. 1988 Aug;29(8):1235-41. Invest Ophthalmol Vis Sci. 1988. PMID: 3417410

6

Retinal dysfunction in central serous retinopathy.

Chuang EL, Sharp DM, Fitzke FW, Kemp CM, Holden AL, Bird AC. Chuang EL, et al. Among authors: kemp cm. Eye (Lond). 1987;1 ( Pt 1):120-5. doi: 10.1038/eye.1987.18. Eye (Lond). 1987. PMID: 3556651

7

Retinal function and rhodopsin levels in autosomal dominant retinitis pigmentosa with rhodopsin mutations.

Jacobson SG, Kemp CM, Sung CH, Nathans J. Jacobson SG, et al. Among authors: kemp cm. Am J Ophthalmol. 1991 Sep 15;112(3):256-71. doi: 10.1016/s0002-9394(14)76726-1. Am J Ophthalmol. 1991. PMID: 1882937 Free article.

8

Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosa.

Jacobson SG, Kemp CM, Cideciyan AV, Macke JP, Sung CH, Nathans J. Jacobson SG, et al. Among authors: kemp cm. Invest Ophthalmol Vis Sci. 1994 Apr;35(5):2521-34. Invest Ophthalmol Vis Sci. 1994. PMID: 8163341

9

Vitamin A treatment for night blindness in primary biliary cirrhosis.

Walt RP, Kemp CM, Lyness L, Bird AC, Sherlock S. Walt RP, et al. Among authors: kemp cm. Br Med J (Clin Res Ed). 1984 Apr 7;288(6423):1030-1. doi: 10.1136/bmj.288.6423.1030. Br Med J (Clin Res Ed). 1984. PMID: 6423181 Free PMC article.

10

RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor function.

Kemp CM, Jacobson SG, Cideciyan AV, Kimura AE, Sheffield VC, Stone EM. Kemp CM, et al. Invest Ophthalmol Vis Sci. 1994 Jul;35(8):3154-62. Invest Ophthalmol Vis Sci. 1994. PMID: 8045710

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