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Comparing the RETeval® portable ERG device with more traditional tabletop ERG systems in normal subjects and selected retinopathies

Documenta ophthalmologica, 2023-04, Vol.146 (2), p.137-150

2023

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Organic visual loss measured by kinetic perimetry and retinal electrophysiology in children with functional amblyopia

Documenta ophthalmologica, 2021-08, Vol.143 (1), p.1-16

2021

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Ring analysis of multifocal oscillatory potentials (mfOPs) in cCSNB suggests near-normal ON–OFF pathways at the fovea only

Documenta ophthalmologica, 2020-10, Vol.141 (2), p.99-109

2020

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Revealing a retinal facilitatory effect with the multifocal ERG

Documenta ophthalmologica, 2019-04, Vol.138 (2), p.117-124

2019

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Optic pathway gliomas in patients with neurofibromatosis type 1: Follow-up of 44 patients

Journal of AAPOS, 2010-04, Vol.14 (2), p.155-158

2010

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Mutations in NYX , encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness

Nature genetics, 2000-11, Vol.26 (3), p.319-323

2000

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The photopic ERG luminance-response function (photopic hill): method of analysis and clinical application

Vision research (Oxford), 2003-06, Vol.43 (12), p.1405-1412

2003

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Prevalence and Severity of Hypertensive Retinopathy in Children

Clinical pediatrics, 2009-11, Vol.48 (9), p.926-930

2009

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Optimal compliance for amblyopia therapy: occlusion with a translucent tape on the lens

Canadian journal of ophthalmology, 2009-10, Vol.44 (5), p.523-528

2009

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A first description of chronic arthritis and uveitis in an adolescent girl with glycogen storage disease

Pediatric rheumatology online journal, 2012-07, Vol.10 (S1), p.A93-A93, Article A93

2012

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Acquired restrictive strabismus and high axial myopia: diagnosis and management

Canadian journal of ophthalmology, 2009-08, Vol.44 (4), p.437-440

2009

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Congenital mydriasis: spontaneous resolution in one of two cases

Canadian journal of ophthalmology, 2005-04, Vol.40 (2), p.204-207

2005

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Resolution of periodic alternating nystagmus after decompression for Chiari malformation

Canadian journal of ophthalmology, 2005-12, Vol.40 (6), p.778-780

2005

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Ophthalmic complications of slit-ventricle syndrome in children

Ophthalmology (Rochester, Minn.), 2002-03, Vol.109 (3), p.520-524

2002

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Presumed endogenous Klebsiella pneumonia endophthalmitis in a premature infant

Journal of AAPOS, 2004-08, Vol.8 (4), p.398-400

2004

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Localization of the Usher Syndrome Type ID Gene (Ush1D) to Chromosome 10

Human molecular genetics, 1996-10, Vol.5 (10), p.1689-1692

1996

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Ophthalmic complications of slit-ventricle syndrome in children. Discussion

Ophthalmology (Rochester, Minn.), 2002, Vol.109 (3), p.520-525

2002

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Evidence supportive of a functional discrimination between photopic oscillatory potentials as revealed with cone and rod mediated retinopathies

Documenta ophthalmologica, 1998, Vol.95 (1), p.35-54

1998

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Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome)

Pediatric neurology, 1996-11, Vol.15 (4), p.337-339

1996

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Clinical Evaluation of Aminocaproic, Acid for Managing Traumatic Hyphema in Children

Ophthalmology (Rochester, Minn.), 1995-11, Vol.102 (11), p.1646-1653

1995

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Human strabismus: Evaluation of the interhemispheric transmission time and hemiretinal differences using a reaction time task

Behavioural brain research, 1994-05, Vol.62 (1), p.63-70

1994

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Monocular contribution to the peak time of the binocular pattern visual evoked potential

Documenta ophthalmologica, 1995-01, Vol.91 (2), p.181-193

1995

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Sandhoff's disease (GM2 gangliosidosis type 2). Histopathology and ultrastructure of the eye

Archives of ophthalmology (1960), 1980-06, Vol.98 (6), p.1089

1980

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Optic nerve in globoid leukodystrophy (Krabbe's disease). Ultrastructural changes

Archives of ophthalmology (1960), 1978-05, Vol.96 (5), p.864

1978

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Importance of an Eye Examination in Identifying the Cause of Congenital Hearing Impairment

The Journal of speech and hearing disorders, 1981-08, Vol.46 (3), p.258-261

1981

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Comparing the RETeval® portable ERG device with more traditional tabletop ERG systems in normal subjects and selected retinopathies

Organic visual loss measured by kinetic perimetry and retinal electrophysiology in children with functional amblyopia

Ring analysis of multifocal oscillatory potentials (mfOPs) in cCSNB suggests near-normal ON–OFF pathways at the fovea only

Revealing a retinal facilitatory effect with the multifocal ERG

Optic pathway gliomas in patients with neurofibromatosis type 1: Follow-up of 44 patients

Mutations in NYX , encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness

The photopic ERG luminance-response function (photopic hill): method of analysis and clinical application

Prevalence and Severity of Hypertensive Retinopathy in Children

Optimal compliance for amblyopia therapy: occlusion with a translucent tape on the lens

A first description of chronic arthritis and uveitis in an adolescent girl with glycogen storage disease

Acquired restrictive strabismus and high axial myopia: diagnosis and management

Congenital mydriasis: spontaneous resolution in one of two cases

Resolution of periodic alternating nystagmus after decompression for Chiari malformation

Ophthalmic complications of slit-ventricle syndrome in children

Presumed endogenous Klebsiella pneumonia endophthalmitis in a premature infant

Localization of the Usher Syndrome Type ID Gene (Ush1D) to Chromosome 10

Ophthalmic complications of slit-ventricle syndrome in children. Discussion

Evidence supportive of a functional discrimination between photopic oscillatory potentials as revealed with cone and rod mediated retinopathies

Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome)

Clinical Evaluation of Aminocaproic, Acid for Managing Traumatic Hyphema in Children

Human strabismus: Evaluation of the interhemispheric transmission time and hemiretinal differences using a reaction time task

Monocular contribution to the peak time of the binocular pattern visual evoked potential

Sandhoff's disease (GM2 gangliosidosis type 2). Histopathology and ultrastructure of the eye

Optic nerve in globoid leukodystrophy (Krabbe's disease). Ultrastructural changes

Importance of an Eye Examination in Identifying the Cause of Congenital Hearing Impairment

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