'Unilateral cone dystrophy': ERG changes implicate abnormal signaling by hyperpolarizing bipolar and/or horizontal cells.

Por Sieving, P A
Publicado em 1994

Photopic ON- and OFF-pathway abnormalities in retinal dystrophies.

Por Sieving, P A
Publicado em 1993

Refractive errors of retinitis pigmentosa patients.

Por Sieving, P A, Fishman, G A
Publicado em 1978

Juvenile retinoschisis: a model for molecular diagnostic testing of X-linked ophthalmic disease.

Por Sieving, P A, Yashar, B M, Ayyagari, R
Publicado em 1999

Sorsby's fundus dystrophy in a family with a Ser-181-CVS mutation in the TIMP-3 gene: poor outcome after laser photocoagulation.

Por Sieving, P A, Boskovich, S, Bingham, E, Pawar, H
Publicado em 1996

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

Por Sieving, P A, Fishman, G A, Salzano, T, Rabb, M F
Publicado em 1984

Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation.

Por Sieving, P A, Richards, J E, Naarendorp, F, Bingham, E L, Scott, K, Alpern, M
Publicado em 1995

Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes.

Por Sieving, P A, Bingham, E L, Roth, M S, Young, M R, Boehnke, M, Kuo, C Y, Ginsburg, D
Publicado em 1990

Molecular modeling of retinoschisin with functional analysis of pathogenic mutations from human X-linked retinoschisis

Por Sergeev, Y.V., Caruso, R.C., Meltzer, M.R., Smaoui, N., MacDonald, I.M., Sieving, P.A.
Publicado em 2010

Protein-truncation mutations in the RP2 gene in a North American cohort of families with X-linked retinitis pigmentosa.

Por Mears, A J, Gieser, L, Yan, D, Chen, C, Fahrner, S, Hiriyanna, S, Fujita, R, Jacobson, S G, Sieving, P A, Swaroop, A
Publicado em 1999

Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families.

Por Fujita, R, Buraczynska, M, Gieser, L, Wu, W, Forsythe, P, Abrahamson, M, Jacobson, S G, Sieving, P A, Andréasson, S, Swaroop, A
Publicado em 1997

A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3.

Por Fujita, R., Bingham, E., Forsythe, P., McHenry, C., Aita, V., Navia, B. A., Dry, K., Segal, M., Devoto, M., Bruns, G., Wright, A. F., Ott, J., Sieving, P. A., Swaroop, A.
Publicado em 1996

Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa.

Por Buraczynska, M, Wu, W, Fujita, R, Buraczynska, K, Phelps, E, Andréasson, S, Bennett, J, Birch, D G, Fishman, G A, Hoffman, D R, Inana, G, Jacobson, S G, Musarella, M A, Sieving, P A, Swaroop, A
Publicado em 1997