Fishman GA - Search Results

1

X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60.

Fishman GA, Grover S, Jacobson SG, Alexander KR, Derlacki DJ, Wu W, Buraczynska M, Swaroop A. Fishman GA, et al. Ophthalmology. 1998 Dec;105(12):2286-96. doi: 10.1016/S0161-6420(98)91231-3. Ophthalmology. 1998. PMID: 9855162 Free article.

2

Comparison of intraocular light scatter in carriers of choroideremia and X-linked retinitis pigmentosa.

Grover S, Alexander KR, Fishman GA, Ryan J. Grover S, et al. Among authors: fishman ga. Ophthalmology. 2002 Jan;109(1):159-63. doi: 10.1016/s0161-6420(01)00854-5. Ophthalmology. 2002. PMID: 11772598

3

A distinctive form of congenital stationary night blindness with cone ON-pathway dysfunction.

Barnes CS, Alexander KR, Fishman GA. Barnes CS, et al. Among authors: fishman ga. Ophthalmology. 2002 Mar;109(3):575-83. doi: 10.1016/s0161-6420(01)00981-2. Ophthalmology. 2002. PMID: 11874764

4

Atypical presentation of pattern dystrophy in two families with peripherin/RDS mutations.

Grover S, Fishman GA, Stone EM. Grover S, et al. Among authors: fishman ga. Ophthalmology. 2002 Jun;109(6):1110-7. doi: 10.1016/s0161-6420(02)01029-1. Ophthalmology. 2002. PMID: 12045052

5

Deficits in temporal integration for contrast processing in retinitis pigmentosa.

Alexander KR, Barnes CS, Fishman GA. Alexander KR, et al. Among authors: fishman ga. Invest Ophthalmol Vis Sci. 2003 Jul;44(7):3163-9. doi: 10.1167/iovs.02-0812. Invest Ophthalmol Vis Sci. 2003. PMID: 12824267

6

ON-pathway dysfunction and timing properties of the flicker ERG in carriers of X-linked retinitis pigmentosa.

Alexander KR, Barnes CS, Fishman GA. Alexander KR, et al. Among authors: fishman ga. Invest Ophthalmol Vis Sci. 2003 Sep;44(9):4017-25. doi: 10.1167/iovs.02-0989. Invest Ophthalmol Vis Sci. 2003. PMID: 12939324

7

Novel mutations in the cellular retinaldehyde-binding protein gene (RLBP1) associated with retinitis punctata albescens: evidence of interfamilial genetic heterogeneity and fundus changes in heterozygotes.

Fishman GA, Roberts MF, Derlacki DJ, Grimsby JL, Yamamoto H, Sharon D, Nishiguchi KM, Dryja TP. Fishman GA, et al. Arch Ophthalmol. 2004 Jan;122(1):70-5. doi: 10.1001/archopht.122.1.70. Arch Ophthalmol. 2004. PMID: 14718298

8

The application of chromatic dark-adapted kinetic perimetry to retinal diseases.

Rotenstreich Y, Fishman GA, Lindeman M, Alexander KR. Rotenstreich Y, et al. Among authors: fishman ga. Ophthalmology. 2004 Jun;111(6):1222-7. doi: 10.1016/j.ophtha.2003.10.025. Ophthalmology. 2004. PMID: 15177975

9

A novel IMPDH1 mutation (Arg231Pro) in a family with a severe form of autosomal dominant retinitis pigmentosa.

Grover S, Fishman GA, Stone EM. Grover S, et al. Among authors: fishman ga. Ophthalmology. 2004 Oct;111(10):1910-6. doi: 10.1016/j.ophtha.2004.03.039. Ophthalmology. 2004. PMID: 15465556

10

Contrast sensitivity deficits in inferred magnocellular and parvocellular pathways in retinitis pigmentosa.

Alexander KR, Barnes CS, Fishman GA, Pokorny J, Smith VC. Alexander KR, et al. Among authors: fishman ga. Invest Ophthalmol Vis Sci. 2004 Dec;45(12):4510-9. doi: 10.1167/iovs.04-0188. Invest Ophthalmol Vis Sci. 2004. PMID: 15557462

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