(Q35591993)

9 August 2017

Oligocone trichromacy: a rare and unusual cone dysfunction syndrome (English)

1 reference

9 August 2017

oligocone trichromacy

1 reference

Mollon JD

5

0 references

author name string

Michaelides M

1

1 reference

9 August 2017

Holder GE

2

1 reference

9 August 2017

Bradshaw K

3

1 reference

9 August 2017

Hunt DM

4

1 reference

9 August 2017

Moore AT

6

1 reference

9 August 2017

language of work or name

English

0 references

publication date

1 April 2004

1 reference

British Journal of Ophthalmology

9 August 2017

1 reference

9 August 2017

88

1 reference

9 August 2017

4

1 reference

9 August 2017

497-500

1 reference

Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsia

9 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772119

Pattern electroretinography (PERG) and an integrated approach to visual pathway diagnosis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772119

Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772119

Assessing retinal function with the multifocal technique

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772119

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772119

Standard for clinical electro-oculography. International Society for Clinical Electrophysiology of Vision.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772119

Differential diagnosis of typical and atypical congenital achromatopsia. Analysis of a progressive foveal dystrophy and a nonprogressive oligo-cone trichromasy (general cone dysfunction without achromatopsia), both of which at first had been diagnos

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772119

Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the alpha subunit of cone transducin (GNAT2)

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772119

Standard for pattern electroretinography. International Society for Clinical Electrophysiology of Vision.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772119

Genetic basis of total colourblindness among the Pingelapese islanders

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772119

Standard for clinical electroretinography (1999 update). International Society for Clinical Electrophysiology of Vision.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772119

["Oligocone" trichromasy, a rare form of incomplete achromatopsia].

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772119

CONE DYSFUNCTION SYNDROMES

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15031164

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Luminance noise and the rapid determination of discrimination ellipses in colour deficiency

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15031164

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

https://pubmed.ncbi.nlm.nih.gov/15031164

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/BJO.2003.028142

1 reference

9 August 2017

1 reference

9 August 2017

1 reference