(Q57223613)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1550184%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

title

Abnormal rod dark adaptation in autosomal dominant retinitis pigmentosa with proline-23-histidine rhodopsin mutation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1550184%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

1 reference

1 reference

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7 October 2022

5

J. Nathans

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1550184

7 October 2022

author name string

C. M. Kemp

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1550184

7 October 2022

S. G. Jacobson

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1550184

7 October 2022

A. J. Roman

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1550184

7 October 2022

C. H. Sung

4

1 reference

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7 October 2022

language of work or name

English

0 references

publication date

1 February 1992

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1550184%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

15 February 1992

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1550184

American Journal of Ophthalmology

7 October 2022

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1550184%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

volume

113

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1550184%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

issue

2

1 reference

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21 September 2019

page(s)

165-174

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1550184%20AND%20SRC:MED&resulttype=core&format=json

Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3

21 September 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

Rhodopsin mutations in autosomal dominant retinitis pigmentosa

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

Autosomal dominant retinitis pigmentosa: Four new mutations in rhodopsin, one of them in the retinal attachment site

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucine

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

Retinal function and rhodopsin levels in autosomal dominant retinitis pigmentosa with rhodopsin mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

Ocular findings associated with a rhodopsin gene codon 58 transversion mutation in autosomal dominant retinitis pigmentosa.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

Prolonged rod dark adaptation in retinitis pigmentosa

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

Interocular asymmetry of visual function in heterozygotes of X-linked retinitis pigmentosa

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

Automated Light- and Dark- Adapted Perimetry for Evaluating Retinitis Pigmentosa

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

Rhodopsin flash photolysis in man

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

Human rhodopsin measurement using a T.V.-based imaging fundus reflectometer

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

Two forms of autosomal dominant primary retinitis pigmentosa

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

A clinical, psychophysical, and electroretinographic survey of patients with autosomal dominant retinitis pigmentosa

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

The involvement of rod photoreceptors in dark adaptation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

Patterns of rod and cone dysfunction in Bardet-Biedl syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971529-6

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0002-9394(14)71529-6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1550184%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

1 reference