Sieving PA - Search Results

1

Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration.

Swain PK, Chen S, Wang QL, Affatigato LM, Coats CL, Brady KD, Fishman GA, Jacobson SG, Swaroop A, Stone E, Sieving PA, Zack DJ. Swain PK, et al. Among authors: sieving pa. Neuron. 1997 Dec;19(6):1329-36. doi: 10.1016/s0896-6273(00)80423-7. Neuron. 1997. PMID: 9427255 Free article.

2

Refractive errors of retinitis pigmentosa patients.

Sieving PA, Fishman GA. Sieving PA, et al. Br J Ophthalmol. 1978 Mar;62(3):163-7. doi: 10.1136/bjo.62.3.163. Br J Ophthalmol. 1978. PMID: 638108 Free PMC article.

3

Corneal wick electrode for recording bright flash electroretinograms and early receptor potentials.

Sieving PA, Fishman GA, Maggiano JM. Sieving PA, et al. Arch Ophthalmol. 1978 May;96(5):899-900. doi: 10.1001/archopht.1978.03910050501024. Arch Ophthalmol. 1978. PMID: 655931

4

Early receptor potential measurements in human ocular siderosis.

Sieving PA, Fishman GA, Alexander KR, Goldberg MF. Sieving PA, et al. Arch Ophthalmol. 1983 Nov;101(11):1716-20. doi: 10.1001/archopht.1983.01040020718010. Arch Ophthalmol. 1983. PMID: 6639427

5

Acute macular neuroretinopathy: early receptor potential change suggests photoreceptor pathology.

Sieving PA, Fishman GA, Salzano T, Rabb MF. Sieving PA, et al. Br J Ophthalmol. 1984 Apr;68(4):229-34. doi: 10.1136/bjo.68.4.229. Br J Ophthalmol. 1984. PMID: 6704358 Free PMC article.

6

Multiple evanescent white dot syndrome. I. Clinical findings.

Jampol LM, Sieving PA, Pugh D, Fishman GA, Gilbert H. Jampol LM, et al. Among authors: sieving pa. Arch Ophthalmol. 1984 May;102(5):671-4. doi: 10.1001/archopht.1984.01040030527008. Arch Ophthalmol. 1984. PMID: 6721749

7

Multiple evanescent white dot syndrome. II. Electrophysiology of the photoreceptors during retinal pigment epithelial disease.

Sieving PA, Fishman GA, Jampol LM, Pugh D. Sieving PA, et al. Arch Ophthalmol. 1984 May;102(5):675-9. doi: 10.1001/archopht.1984.01040030531009. Arch Ophthalmol. 1984. PMID: 6721750

8

Disruption of conserved rhodopsin disulfide bond by Cys187Tyr mutation causes early and severe autosomal dominant retinitis pigmentosa.

Richards JE, Scott KM, Sieving PA. Richards JE, et al. Among authors: sieving pa. Ophthalmology. 1995 Apr;102(4):669-77. doi: 10.1016/s0161-6420(95)30972-4. Ophthalmology. 1995. PMID: 7724183

9

Dinucleotide repeat polymorphism at the DXS977 locus.

Yan D, Wong D, Zheng K, Thiselton D, Fujita R, Sieving PA, Bhattacharya SS, Yang-Feng TL, Richards JE, Swaroop A. Yan D, et al. Among authors: sieving pa. Hum Mol Genet. 1994 Jun;3(6):1030. doi: 10.1093/hmg/3.6.1030. Hum Mol Genet. 1994. PMID: 7951222 No abstract available.

10

Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsin.

Macke JP, Davenport CM, Jacobson SG, Hennessey JC, Gonzalez-Fernandez F, Conway BP, Heckenlively J, Palmer R, Maumenee IH, Sieving P, et al. Macke JP, et al. Am J Hum Genet. 1993 Jul;53(1):80-9. Am J Hum Genet. 1993. PMID: 8317502 Free PMC article.

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