Gerald Allen Fishman

Summary

Affiliation: University of Illinois at Chicago
Country: USA

Publications

  1. ncbi Short-term inter-visit variability of erg amplitudes in normal subjects and patients with retinitis pigmentosa
    Gerald A Fishman
    Department of Ophthalmology and Visual Science, University of Illinois at Chicago, IL 60612, USA
    Retina 25:1014-21. 2005
  2. ncbi Multifocal ERG findings in carriers of X-linked retinoschisis
    Linda S Kim
    Department of Ophthalmology and Visual Sciences, College of Medicine, University of Illinois at Chicago, Eye and Ear Infirmary, 1855 West Taylor Street, Chicago, IL 60612 7234, USA
    Doc Ophthalmol 114:21-6. 2007
  3. ncbi Historical evolution in the understanding of Stargardt macular dystrophy
    Gerald Allen Fishman
    Department of Ophthalmology and Visual Sciences, University of Illinois Eye and Ear Infirmary, Chicago, Illinois 60612, USA
    Ophthalmic Genet 31:183-9. 2010
  4. ncbi John dalton: though in error, he still influenced our understanding of congenital color deficiency
    Gerald A Fishman
    Department of Ophthalmology and Visual Science, Illinois Eye and Ear Infirmary, University of Illinois at Chicago, Illinois 60612 7243, USA
    Ophthalmic Genet 29:162-5. 2008
  5. ncbi Natural course of visual field loss in patients with Type 2 Usher syndrome
    Gerald A Fishman
    Department of Ophthalmology and Visual Sciences, UIC Eye Center, University of Illinois at Chicago, 1855 W Taylor Street, Chicago, IL 60612, USA
    Retina 27:601-8. 2007
  6. ncbi Continued use of dorzolamide for the treatment of cystoid macular oedema in patients with retinitis pigmentosa
    Gerald A Fishman
    Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, IL 60612, USA
    Br J Ophthalmol 91:743-5. 2007
  7. ncbi A new 2-base pair deletion in the RPGR gene in a black family with X-linked retinitis pigmentosa
    G A Fishman
    Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago Eye Center, 60612, USA
    Arch Ophthalmol 116:213-8. 1998
  8. ncbi Outcome measures and their application in clinical trials for retinal degenerative diseases: outline, review, and perspective
    Gerald A Fishman
    Department of Ophthalmology and Visual Sciences, University of Illinois, Chicago, Illinois, USA
    Retina 25:772-7. 2005
  9. ncbi 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
    Gerald A Fishman
    Department of Ophthalmology and Visual Sciences, UIC Eye Center, University of Illinois at Chicago, 60612, USA
    Arch Ophthalmol 122:70-5. 2004
  10. ncbi ABCA4 gene sequence variations in patients with autosomal recessive cone-rod dystrophy
    Gerald A Fishman
    Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, 60612, USA
    Arch Ophthalmol 121:851-5. 2003

Detail Information

Publications12

  1. ncbi Short-term inter-visit variability of erg amplitudes in normal subjects and patients with retinitis pigmentosa
    Gerald A Fishman
    Department of Ophthalmology and Visual Science, University of Illinois at Chicago, IL 60612, USA
    Retina 25:1014-21. 2005
    ..To evaluate the short-term test/retest variability in visually normal subjects and patients with retinitis pigmentosa (RP), and to assess the effect of stimulus intensity and baseline amplitude on electroretinogram (ERG) variability...
  2. ncbi Multifocal ERG findings in carriers of X-linked retinoschisis
    Linda S Kim
    Department of Ophthalmology and Visual Sciences, College of Medicine, University of Illinois at Chicago, Eye and Ear Infirmary, 1855 West Taylor Street, Chicago, IL 60612 7234, USA
    Doc Ophthalmol 114:21-6. 2007
    ..To determine whether retinal dysfunction in obligate carriers of X-linked retinoschisis (XLRS) could be observed in local electroretinographic responses obtained with the multifocal electroretinogram (mfERG)...
  3. ncbi Historical evolution in the understanding of Stargardt macular dystrophy
    Gerald Allen Fishman
    Department of Ophthalmology and Visual Sciences, University of Illinois Eye and Ear Infirmary, Chicago, Illinois 60612, USA
    Ophthalmic Genet 31:183-9. 2010
    ....
  4. ncbi John dalton: though in error, he still influenced our understanding of congenital color deficiency
    Gerald A Fishman
    Department of Ophthalmology and Visual Science, Illinois Eye and Ear Infirmary, University of Illinois at Chicago, Illinois 60612 7243, USA
    Ophthalmic Genet 29:162-5. 2008
    ..Further generations later, DNA analyses by PCR conclusively recorded the specific color deficiency (deuteranopia) with which Dalton was affected...
  5. ncbi Natural course of visual field loss in patients with Type 2 Usher syndrome
    Gerald A Fishman
    Department of Ophthalmology and Visual Sciences, UIC Eye Center, University of Illinois at Chicago, 1855 W Taylor Street, Chicago, IL 60612, USA
    Retina 27:601-8. 2007
    ..To evaluate the natural course of visual field loss in patients with Type 2 Usher syndrome and different patterns of visual field loss...
  6. ncbi Continued use of dorzolamide for the treatment of cystoid macular oedema in patients with retinitis pigmentosa
    Gerald A Fishman
    Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, IL 60612, USA
    Br J Ophthalmol 91:743-5. 2007
    ..To determine the value of a topical carbonic anhydrase inhibitor for extended treatment of cystoid macular oedema (CME) in patients with retinitis pigmentosa (RP)...
  7. ncbi A new 2-base pair deletion in the RPGR gene in a black family with X-linked retinitis pigmentosa
    G A Fishman
    Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago Eye Center, 60612, USA
    Arch Ophthalmol 116:213-8. 1998
    ..To report the genetic and ophthalmic findings in a black family with X-linked retinitis pigmentosa resulting from a newly identified mutation in the RPGR (retinitis pigmentosa GTPase regulator) gene...
  8. ncbi Outcome measures and their application in clinical trials for retinal degenerative diseases: outline, review, and perspective
    Gerald A Fishman
    Department of Ophthalmology and Visual Sciences, University of Illinois, Chicago, Illinois, USA
    Retina 25:772-7. 2005
  9. ncbi 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
    Gerald A Fishman
    Department of Ophthalmology and Visual Sciences, UIC Eye Center, University of Illinois at Chicago, 60612, USA
    Arch Ophthalmol 122:70-5. 2004
    ..To evaluate the molecular genetic defects associated with retinitis punctata albescens (RPA) in 5 patients from 3 families with this disease...
  10. ncbi ABCA4 gene sequence variations in patients with autosomal recessive cone-rod dystrophy
    Gerald A Fishman
    Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, 60612, USA
    Arch Ophthalmol 121:851-5. 2003
    ..To identify sequence variations in the ABCA4 gene in a cohort of patients with autosomal recessive cone-rod dystrophy...
  11. ncbi Variation of clinical expression in patients with Stargardt dystrophy and sequence variations in the ABCR gene
    G A Fishman
    Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, 60612, USA
    Arch Ophthalmol 117:504-10. 1999
    ..To report the spectrum of ophthalmic findings in patients with Stargardt dystrophy or fundus flavimaculatus who have a specific sequence variation in the ABCR gene...
  12. ncbi Spectral-domain OCT peripapillary retinal nerve fibre layer thickness measurements in patients with Stargardt disease
    Mohamed A Genead
    Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, Illinois, USA
    Br J Ophthalmol 95:689-93. 2011
    ..To evaluate the presence of peripapillary retinal nerve fibre layer (RNFL) defects in patients with Stargardt disease by using spectral-domain optical coherence tomography (SD-OCT)...