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ARVO Annual Meeting Abstract May 2006

Screen for Mutations the Lecithin Retinol Acyltransferase (LRAT) Gene in Patients With Leber Congenital Amaurosis and Autosomal Recessive Retinitis Pigmentosa

M.O. Sweeney; T.L. McGee; E.L. Berson; T.P. Dryja

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):1685. doi:

ARVO Annual Meeting Abstract May 2006

A Screen for Mutations in the GNB1 Gene in Patients With Autosomal Dominant Retinitis Pigmentosa

G.H. Mylvaganam; T.L. McGee; E.L. Berson; T.P. Dryja

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):1702. doi:

ARVO Annual Meeting Abstract May 2006

Disease Progression in Patients with X–Linked Retinitis Pigmentosa Due to RPGR Gene Mutations

M.A. Sandberg; B. Rosner; C. Weigel–DiFranco; E.L. Berson

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):4343. doi:

ARVO Annual Meeting Abstract May 2006

Search for Recessive Retinitis Pigmentosa Genes Using Microarray Analysis of RNA Expression Levels in Lymphoblasts

D.T. Hartong; T.L. McGee; N. Gorji; E.L. Berson; T.P. Dryja

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):5521. doi:

ARVO Annual Meeting Abstract May 2005

Association Between Visual Acuity and Central Retinal Thickness in Retinitis Pigmentosa

M.A. Sandberg; A.R. Gaudio; R. Brockhurst; E.L. Berson

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):516. doi:

ARVO Annual Meeting Abstract May 2005

Screening of 51 Newly Identified USH2A Exons Among Patients With Usher Syndrome Type II and Non–Syndromic Recessive Retinitis Pigmentosa

B. Jian Seyedahmadi; E.L. Berson; T.P. Dryja

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):1801. doi:

ARVO Annual Meeting Abstract May 2005

A Screen for Mutations of the Aipl1 Gene in Patients With Supernormal Scotopic Erg B–Wave

S.M. Adams; R.G. Weleber; E.L. Berson; T.P. Dryja

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):1820. doi:

ARVO Annual Meeting Abstract May 2005

Analysis of Exons Specific to the Go1 Transcript of the Bipolar G–Protein in Patients With Congenital Stationary Night Blindness

A.K. Alt; T.L. McGee; E.L. Berson; T.P. Dryja

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):1821. doi:

ARVO Annual Meeting Abstract May 2005

Recessive Mutations in the CYP4V2 Gene in East Asian and Middle Eastern Patients With Bietti Crytalline Corneoretinal Dystrophy

M. Nakamura; K.M. Nishiguchi; J. Lin; T.P. Dryja; E.L. Berson; Y. Miyake

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):1832. doi:

ARVO Annual Meeting Abstract May 2005

Mutations in the GRM6 Gene Encoding the Mglur6 Receptor in Patients With Autosomal Recessive Night Blindness and Abnormal Cone ERG on Responses

T.L. McGee; E.L. Berson; M.A. Sandberg; K.R. Alexander; A.S. Rajagopalan; G.A. Fishman; D.J. Derlacki; T.P. Dryja

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):2290. doi:

ARVO Annual Meeting Abstract May 2005

Rod and Cone Opsin Mislocalization in an Autopsy Eye From a Female Carrier of X–linked RP With a Gly436Asp Mutation in the RPGR Gene

M. Adamian; B. Pawlyk; D.–H. Hong; E.L. Berson

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):3400. doi:

ARVO Annual Meeting Abstract May 2004

Defects in RGS9 or its anchor protein R9AP in patients with bradyopsia, a novel form of retinal dysfunction

K. Nishiguchi; M.A. Sandberg; A.C. Kooijman; K.A. Martemyanov; J.W. R. Pott; S.A. Hagstrom; V.Y. Arshavsky; E.L. Berson; T.P. Dryja

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):1020. doi:

ARVO Annual Meeting Abstract May 2004

EXTENDED WEARING TRIAL OF TRIFIELD PRISM VISUAL AID FOR "TUNNEL VISION" AMONG PATIENTS WITH RETINITIS PIGMENTOSA OR CHOROIDEREMIA

D.W. Stringer; R.L. Woods; R.B. Goldstein; E. Peli; E.L. Berson; R.D. Easton; T. Bond

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):1400. doi:

ARVO Annual Meeting Abstract May 2004

A SCREEN FOR MUTATIONS OF THE IMPG1 GENE IN PATIENTS WITH RETINITIS PIGMENTOSA

S.M. Adams; T.P. Dryja; E.L. Berson

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):2445. doi:

ARVO Annual Meeting Abstract May 2004

Search for mutations in the peropsin gene, an RPE–specific rhodopsin homolog, in patients with inherited retinal degeneration

C. Rivolta; E.L. Berson; T.P. Dryja

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):2447. doi:

ARVO Annual Meeting Abstract May 2004

USH3A mutations in patients with a prior diagnosis of Usher syndrome type I, Usher syndrome type II, and nonsyndromic recessive retinitis pigmentosa

B. Jian Seyedahmadi; E.L. Berson; T.P. Dryja

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):4726. doi:

ARVO Annual Meeting Abstract May 2004

Meta–Analysis of Histopathologic–Genotype Correlations in Human Retinal Degeneration

Y. Ben Arie–Weintrob; E.L. Berson; T.P. Dryja

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):5087. doi:

ARVO Annual Meeting Abstract May 2004

Disease Expression in Patients with USH2A Mutations

M.A. Sandberg; B. Jian Seyedahmadi; C. Weigel–DiFranco; T.P. Dryja; E.L. Berson

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):5089. doi:

ARVO Annual Meeting Abstract May 2004

Natural Course of Ocular Function in Pigmented Paravenous Retinochoroidal Atrophy

J.Y. Choi; M.A. Sandberg; C.A. Ling; E.L. Berson

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):5118. doi:

ARVO Annual Meeting Abstract May 2003

Mutation Survey of the RP2 and RPGR Genes (Including ORF15) and Evidence for Genotype-Phenotype Correlations

D. Sharon; M.A. Sandberg; V.W. Rabe; M. Stilberger; T.P. Dryja; E.L. Berson

Invest. Ophthalmol. Vis. Sci.. 2003; 44(13):1481. doi:

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