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Effects of chronic exposure to hydroxychloroquine or chloroquine on inner retinal structures

Eye (London), 2010-02, Vol.24 (2), p.340-346

2010

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The prevalence of cystoid macular oedema in retinitis pigmentosa patients determined by optical coherence tomography

British journal of ophthalmology, 2008-08, Vol.92 (8), p.1065-1068

2008

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The prevalence of cystoid macular oedema on optical coherence tomography in retinitis pigmentosa patients without cystic changes on fundus examination

Eye (London), 2009-04, Vol.23 (4), p.915-919

2009

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Cystic macular oedema on spectral-domain optical coherence tomography in choroideremia patients without cystic changes on fundus examination

Eye (London), 2011-01, Vol.25 (1), p.84-90

2011

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Selective thinning of the perifoveal inner retina as an early sign of hydroxychloroquine retinal toxicity

Eye (London), 2010-05, Vol.24 (5), p.756-763

2010

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Clinical value, normative retinal sensitivity values, and intrasession repeatability using a combined spectral domain optical coherence tomography scanning laser ophthalmoscope microperimeter

Eye (London), 2011-02, Vol.25 (2), p.245-251

2011

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Mutation of a nuclear receptor gene, NR2E3 , causes enhanced S cone syndrome, a disorder of retinal cell fate

Nature genetics, 2000-02, Vol.24 (2), p.127-131

2000

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Prevalence of cystic macular lesions in patients with Usher II syndrome

Eye (London), 2009-05, Vol.23 (5), p.1206-1209

2009

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An Analysis of Allelic Variation in the ABCA4 Gene

Investigative ophthalmology & visual science, 2001-05, Vol.42 (6), p.1179-1189

2001

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Retrospective, longitudinal, and cross sectional study of visual acuity impairment in choroideraemia

British journal of ophthalmology, 2002-06, Vol.86 (6), p.658-662

2002

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Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or older

Ophthalmology (Rochester, Minn.), 1999-09, Vol.106 (9), p.1780-1785

1999

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Retinal nerve fibre layer thickness analysis in X-linked retinoschisis using Fourier-domain OCT

Eye (London), 2009-05, Vol.23 (5), p.1019-1027

2009

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Allelic Variation in the VMD2 Gene in Best Disease and Age-Related Macular Degeneration

Investigative ophthalmology & visual science, 2000-05, Vol.41 (6), p.1291-1296

2000

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Disease Expression of RP1 Mutations Causing Autosomal Dominant Retinitis Pigmentosa

Investigative ophthalmology & visual science, 2000-06, Vol.41 (7), p.1898-1908

2000

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Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet–Biedl syndrome patient population

Journal of medical genetics, 2010-07, Vol.47 (7), p.453-463

2010

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Rate of Visual Field Loss in Retinitis Pigmentosa

Ophthalmology (Rochester, Minn.), 1997-03, Vol.104 (3), p.460-465

1997

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Attainment of Educational Levels in Patients with Leber’s Congenital Amaurosis

Ophthalmology (Rochester, Minn.), 2006-03, Vol.113 (3), p.481-482

2006

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Patterns of visual field progression in patients with retinitis pigmentosa

Ophthalmology (Rochester, Minn.), 1998-06, Vol.105 (6), p.1069-1075

1998

Volltextzugriff (PDF)

Interocular amplitude differences of the full field electroretinogram in normal subjects

British journal of ophthalmology, 2003-10, Vol.87 (10), p.1268-1271

2003

Volltextzugriff (PDF)

Predicting the pathogenicity of RPE65 mutations

Human mutation, 2009-08, Vol.30 (8), p.1183-1188

2009

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A longitudinal study of visual function in carriers of X-linked recessive retinitis pigmentosa

Ophthalmology (Rochester, Minn.), 2000-02, Vol.107 (2), p.386-396

2000

Volltextzugriff (PDF)

Frequency of Optic Disc or Parapapillary Nerve Fiber Layer Drusen in Retinitis Pigmentosa

Ophthalmology (Rochester, Minn.), 1997-02, Vol.104 (2), p.295-298

1997

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Spectrum of Mutations in the RPGR Gene That Are Identified in 20% of Families with X-Linked Retinitis Pigmentosa

American journal of human genetics, 1997-12, Vol.61 (6), p.1287-1292

1997

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Mutations in the RPE65 Gene in Patients with Autosomal Recessive Retinitis Pigmentosa or Leber Congenital Amaurosis

Proceedings of the National Academy of Sciences - PNAS, 1998-03, Vol.95 (6), p.3088-3093

1998

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Visual Acuity Impairment in Patients with Retinitis Pigmentosa

Ophthalmology (Rochester, Minn.), 1996-10, Vol.103 (10), p.1593-1600

1996

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Effects of chronic exposure to hydroxychloroquine or chloroquine on inner retinal structures

The prevalence of cystoid macular oedema in retinitis pigmentosa patients determined by optical coherence tomography

The prevalence of cystoid macular oedema on optical coherence tomography in retinitis pigmentosa patients without cystic changes on fundus examination

Cystic macular oedema on spectral-domain optical coherence tomography in choroideremia patients without cystic changes on fundus examination

Selective thinning of the perifoveal inner retina as an early sign of hydroxychloroquine retinal toxicity

Clinical value, normative retinal sensitivity values, and intrasession repeatability using a combined spectral domain optical coherence tomography scanning laser ophthalmoscope microperimeter

Mutation of a nuclear receptor gene, NR2E3 , causes enhanced S cone syndrome, a disorder of retinal cell fate

Prevalence of cystic macular lesions in patients with Usher II syndrome

An Analysis of Allelic Variation in the ABCA4 Gene

Retrospective, longitudinal, and cross sectional study of visual acuity impairment in choroideraemia

Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or older

Retinal nerve fibre layer thickness analysis in X-linked retinoschisis using Fourier-domain OCT

Allelic Variation in the VMD2 Gene in Best Disease and Age-Related Macular Degeneration

Disease Expression of RP1 Mutations Causing Autosomal Dominant Retinitis Pigmentosa

Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet–Biedl syndrome patient population

Rate of Visual Field Loss in Retinitis Pigmentosa

Attainment of Educational Levels in Patients with Leber’s Congenital Amaurosis

Patterns of visual field progression in patients with retinitis pigmentosa

Interocular amplitude differences of the full field electroretinogram in normal subjects

Predicting the pathogenicity of RPE65 mutations

A longitudinal study of visual function in carriers of X-linked recessive retinitis pigmentosa

Frequency of Optic Disc or Parapapillary Nerve Fiber Layer Drusen in Retinitis Pigmentosa

Spectrum of Mutations in the RPGR Gene That Are Identified in 20% of Families with X-Linked Retinitis Pigmentosa

Mutations in the RPE65 Gene in Patients with Autosomal Recessive Retinitis Pigmentosa or Leber Congenital Amaurosis

Visual Acuity Impairment in Patients with Retinitis Pigmentosa

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