(Q79353131)

English

Abnormalities of the scotopic threshold response correlated with gene mutation in X-linked retinoschisis and congenital stationary night blindness

scientific article published on 01 September 2003

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14661905%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Abnormalities of the scotopic threshold response correlated with gene mutation in X-linked retinoschisis and congenital stationary night blindness (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14661905%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

night blindness

1 reference

based on heuristic

inferred from title

congenital stationary night blindness

1 reference

based on heuristic

inferred from title

X-linked retinoschisis

1 reference

based on heuristic

inferred from title

author name string

Keith Bradshaw

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14661905%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Douglas Newman

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14661905%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Louise Allen

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14661905%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Anthony Moore

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14661905%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

publication date

1 September 2003

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14661905%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Documenta Ophthalmologica

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14661905%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

107

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14661905%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14661905%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

155-164

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14661905%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

https://scigraph.springernature.com/pub.10.1023/a:1026245931580

0 references

On-response deficit in the electroretinogram of the cone system in X-linked retinoschisis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel CACNA1F mutations in Japanese patients with incomplete congenital stationary night blindness

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electrophysiological similarities between two eyes with X-linked recessive retinoschisis

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The scotopic threshold response of the cat ERG is suppressed selectively by GABA and glycine

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The scotopic electroretinogram of macaque after retinal ganglion cell loss from experimental glaucoma.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Positional cloning of the gene associated with X-linked juvenile retinoschisis

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High correlation between absolute psychophysical threshold and the scotopic threshold response to the same stimulus

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of the XLRS1 gene cause abnormalities of photoreceptor as well as inner retinal responses of the ERG.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital stationary night blindness with negative electroretinogram. A new classification

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Scotopic threshold response in complete and incomplete types of congenital stationary night blindness

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Scotopic threshold response (STR) of the human electroretinogram

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dissecting the dark-adapted electroretinogram

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Photopic ON- and OFF-pathway abnormalities in retinal dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Temporal frequency deficits in the electroretinogram of the cone system in X-linked retinoschisis

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of X-linked retinoschisis protein RS1 in photoreceptor and bipolar cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Origin of deficits in the flicker electroretinogram of the cone system in X-linked retinoschisis as derived from response nonlinearities

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychophysical and electroretinographic findings in X-linked juvenile retinoschisis

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assessing abnormal rod photoreceptor activity with the a-wave of the electroretinogram: applications and methods

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On- and off-responses in photopic electroretinogram in complete and incomplete types of congenital stationary night blindness

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-frequency attenuation of the cone ERG and ON-response deficits in X-linked retinoschisis

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aspartate separation of the scotopic threshold response (STR) from the photoreceptor a-wave of the cat and monkey ERG.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of photoreceptor function and inner retinal activity in juvenile X-linked retinoschisis

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical features in affected males with X-linked retinoschisis

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On- and off-responses in the photopic electroretinogram in complete-type congenital stationary night blindness

1 reference

https://pubmed.ncbi.nlm.nih.gov/14661905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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