Search filters

List of works by David G. Birch

A comparison of visual field sensitivity to photoreceptor thickness in retinitis pigmentosa

scientific article

A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa

scientific article

A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27.

scientific article

A randomized, placebo-controlled clinical trial of docosahexaenoic acid supplementation for X-linked retinitis pigmentosa.

scientific article published in April 2004

A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene

scientific article

Abnormal cone structure in foveal schisis cavities in X-linked retinoschisis from mutations in exon 6 of the RS1 gene.

scientific article

Abnormalities of the retinal cone system in retinitis pigmentosa.

scientific article published in June 1996

Adaptation to polarized light in humans

scientific article published on 01 January 1982

Allelic Heterogeneity and Genetic Modifier Loci Contribute to Clinical Variation in Males with X-Linked Retinitis Pigmentosa Due to RPGR Mutations ⬇️

scientific article published on August 12, 2011

An early nonsense mutation facilitates the expression of a short isoform of CNGA3 by alternative translation initiation

scientific article published on 27 February 2018

ApoER2 function in the establishment and maintenance of retinal synaptic connectivity.

scientific article published on October 2011

Behavioral measurements of rat spectral sensitivity

scientific article published on June 1, 1975

Biological safety assessment of docosahexaenoic acid supplementation in a randomized clinical trial for X-linked retinitis pigmentosa.

scientific article published in September 2003

Characterizing the Phenotype and Genotype of a Family With Occult Macular Dystrophy ⬇️

scientific article published on December 1, 2012

Ciliary neurotrophic factor delivered by encapsulated cell intraocular implants for treatment of geographic atrophy in age-related macular degeneration

scientific article

Comparison of the Goldmann-Weekers dark adaptometer and LKC Technologies Scotopic Sensitivity tester-1

scientific article published on 01 July 2000

Cone and rod ERG phototransduction parameters in retinitis pigmentosa

scientific article published on 01 September 2003

Cone deactivation kinetics and GRK1/GRK7 expression in enhanced S cone syndrome caused by mutations in NR2E3.

scientific article published in March 2003

Control of late off-center cone bipolar cell differentiation and visual signaling by the homeobox gene Vsx1

scientific journal article

Dark adaptation of rod photoreceptors in normal subjects, and in patients with Stargardt disease and an ABCA4 mutation

scientific article

Effect of stimulus size on static visual fields in patients with retinitis pigmentosa.

scientific article published in October 2000

Effects of constant illumination on vision in the albino rat

scientific article published on 01 August 1977

Erratum to: Worldwide Argus II implantation: recommendations to optimize patient outcomes

scientific article published on 29 July 2016

Evidence for genetic heterogeneity in X-linked congenital stationary night blindness.

scientific article

Four-year placebo-controlled trial of docosahexaenoic acid in X-linked retinitis pigmentosa (DHAX trial): a randomized clinical trial

scientific article published on July 2014

GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness

scientific article

Identification of disease-causing mutations in autosomal dominant retinitis pigmentosa (adRP) using next-generation DNA sequencing

scientific article

Increment-threshold functions for different rodent species

scientific article published on 01 March 1975

Interocular amplitude differences of the full field electroretinogram in normal subjects

scientific article published in October 2003

Longitudinal measures in children receiving ENCAD for hereditary retinal degeneration

scientific article published on 01 January 1991

Loss of caveolin-1 impairs retinal function due to disturbance of subretinal microenvironment

scientific article

Macular atrophy in birdshot retinochoroidopathy: an optical coherence tomography and multifocal electroretinography analysis

scientific article

Metabolism of omega-3 fatty acids in patients with autosomal dominant retinitis pigmentosa

scientific article published on 01 March 1995

Mutation analysis identifies GUCY2D as the major gene responsible for autosomal dominant progressive cone degeneration.

scientific article published on 16 May 2008

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

scientific article

Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease

scientific article

Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa

scientific article

Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa

scientific article published on 19 February 2013

Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements

scientific article published on 24 October 2013

Outcome measures and their application in clinical trials for retinal degenerative diseases: outline, review, and perspective.

scientific article

Persistent cone dysfunction in acute exudative polymorphous vitelliform maculopathy

scientific article published on 01 January 2007

Phototransduction in human cones measured using the alpha-wave of the ERG.

scientific article published in October 1995

Polymorphic Variation of RPGRIP1L and IQCB1 as Modifiers of X-Linked Retinitis Pigmentosa Caused by Mutations in RPGR ⬇️

scientific article published on January 1, 2012

Psychophysical studies of cone optical bandwidth in patients with retinitis pigmentosa

scientific article published on 01 January 1982

Red blood cell fatty acid levels in patients with autosomal dominant retinitis pigmentosa

scientific article published on 01 September 1993

Relationships among multifocal electroretinogram amplitude, visual field sensitivity, and SD-OCT receptor layer thicknesses in patients with retinitis pigmentosa

scientific article published on 21 February 2012

Retinal disease in mice lacking hypoxia-inducible transcription factor-2alpha

scientific journal article

Rod photoreceptor temporal properties in retinal degenerative diseases.

scientific article

Rod photoreceptor temporal properties in retinitis pigmentosa.

scientific article

Rod sensitivity, cone sensitivity, and photoreceptor layer thickness in retinal degenerative diseases.

scientific article published on 9 September 2011

Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis.

scientific article published in May 2000

Safety and effect on rod function of ACU-4429, a novel small-molecule visual cycle modulator.

scientific article

Safety assessment of docosahexaenoic acid in X-linked retinitis pigmentosa: the 4-year DHAX trial.

scientific article published on 11 July 2014

Spatial contrast sensitivity in albino and pigmented rats

scientific article published on 01 January 1979

Spectral-domain optical coherence tomography measures of outer segment layer progression in patients with X-linked retinitis pigmentosa.

scientific article

Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis

scientific article

Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa

scientific article published in December 1997

Targeted high-throughput DNA sequencing for gene discovery in retinitis pigmentosa

scientific article

The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations

scientific article

The very large G-protein-coupled receptor VLGR1: a component of the ankle link complex required for the normal development of auditory hair bundles.

scientific article

Transition Zones between Healthy and Diseased Retina in Choroideremia (CHM) and Stargardt Disease (STGD) as Compared to Retinitis Pigmentosa (RP) ⬇️

scientific article published on December 20, 2011

Worldwide Argus II implantation: recommendations to optimize patient outcomes.

scientific article published on 6 May 2016

Paulina is supported by:

About Paulina

Help