(Q46636578)

23 December 2017

title

Progressive cone dystrophy with deutan genotype and phenotype (English)

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23 December 2017

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2

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23 December 2017

Hendrik Scholl

1

object named as

Hendrik P N Scholl

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23 December 2017

author name string

Dorothea Besch

3

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23 December 2017

Eberhart Zrenner

4

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23 December 2017

Herbert Jägle

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23 December 2017

publication date

5 August 2005

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23 December 2017

Graefe's Archive for Clinical and Experimental Ophthalmology

published in

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23 December 2017

volume

244

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23 December 2017

issue

2

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23 December 2017

page(s)

183-191

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23 December 2017

Progressive cone-rod degeneration

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00417-005-0022-7

Cone selective adaptation influences L- and M-cone driven signals in electroretinography and psychophysics.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00417-005-0022-7

Serine-27-Phenylalanine Mutation within the Peripherin/RDS Gene in a Family with Cone Dystrophy

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00417-005-0022-7

Color electroretinography. A method for separation of dysfunctions of cones

21 January 2018

1 reference

12 December 2020

The multifocal electroretinogram (mfERG) and cone isolating stimuli: variation in L- and M-cone driven signals across the retina

1 reference

12 December 2020

Molecular genetics of inherited variation in human color vision

1 reference

12 December 2020

Diagnostic clinical findings of a new syndrome with night blindness, maculopathy, and enhanced S cone sensitivity.

1 reference

12 December 2020

Dominant cone dystrophy starting with blue cone involvement

1 reference

12 December 2020

Human and macaque blue cones studied with electroretinography.

1 reference

12 December 2020

L- and M-cone-driven electroretinograms in Stargardt's macular dystrophy-fundus flavimaculatus.

1 reference

12 December 2020

Response phase of the flicker electroretinogram (ERG) is influenced by cone excitation strength

1 reference

12 December 2020

Autosomal dominantly inherited macular dystrophy with preferential short-wavelength sensitive cone involvement.

1 reference

12 December 2020

Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1

1 reference

12 December 2020

Progressive cone dystrophy

1 reference

12 December 2020

Macular dystrophy with protan genotype and phenotype studied with cone type specific ERGs

1 reference

12 December 2020

Pattern of dysfunction in progressive cone dystrophies--an extended classification

1 reference

12 December 2020

Standard for clinical electroretinography (2004 update).

1 reference

12 December 2020

Blue cone monochromatism: clinical findings in patients with mutations in the red/green opsin gene cluster.

1 reference

12 December 2020

CNGA3 mutations in hereditary cone photoreceptor disorders

1 reference

12 December 2020

An electroretinographic and molecular genetic study of X-linked cone degeneration

1 reference

12 December 2020

Spectral sensitivities of the human cones

1 reference

12 December 2020

L/M cone ratios in human trichromats assessed by psychophysics, electroretinography, and retinal densitometry

1 reference

12 December 2020

Multifocal electroretinogram in trichromat and dichromat observers under cone isolating conditions

1 reference

12 December 2020

Cone spectral sensitivity and chromatic adaptation as revealed by human flicker-electroretinography

1 reference

12 December 2020

Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel

1 reference

12 December 2020

SWS (blue) cone hypersensitivity in a newly identified retinal degeneration.

1 reference

12 December 2020

Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsin

1 reference

12 December 2020

Rod-/L-cone and rod-/M-cone interactions in electroretinograms at different temporal frequencies.

1 reference

12 December 2020

Foveal cone detection statistics in color-normals and dichromats

1 reference

12 December 2020

L- and M-cone driven ERGs are differently altered in Best's macular dystrophy

1 reference

12 December 2020

Selective cone dystrophy with protan genotype.

1 reference

12 December 2020

Alterations of L- and M-cone driven ERGs in cone and cone-rod dystrophies

1 reference

12 December 2020

Spectrum of color gene deletions and phenotype in patients with blue cone monochromacy

1 reference

12 December 2020

Guidelines for basic multifocal electroretinography (mfERG).

1 reference

12 December 2020

L- and M-cone driven large-field and multifocal electroretinograms in sector retinitis pigmentosa

1 reference

12 December 2020

Large phase differences between L-cone- and M-cone-driven electroretinograms in retinitis pigmentosa

1 reference

12 December 2020

Bilateral macular atrophy in blue cone monochromacy (BCM) with loss of the locus control region (LCR) and part of the red pigment gene.

1 reference

12 December 2020

Flicker cone electroretinogram in dichromats and trichromats

1 reference

12 December 2020

Mutation of a conserved cysteine in the X-linked cone opsins causes color vision deficiencies by disrupting protein folding and stability

1 reference

12 December 2020

The density of cones in the fovea centralis of the human dichromat.

1 reference

12 December 2020

CONE DYSFUNCTION SYNDROMES

1 reference

12 December 2020

Cone signal contributions to electroretinograms [correction of electrograms] in dichromats and trichromats

1 reference

12 December 2020

Foveal cone mosaic and visual pigment density in dichromats

1 reference

12 December 2020

10.1007/S00417-005-0022-7

Identifiers

DOI

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23 December 2017

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23 December 2017