Retinal function and rhodopsin levels in autosomal dominant retinitis pigmentosa with rhodopsin mutations (Q34842125)

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Retinal Function and Rhodopsin Levels in Autosomal Dominant Retinitis Pigmentosa With Rhodopsin Mutations

Language	Label	Description	Also known as
English	Retinal function and rhodopsin levels in autosomal dominant retinitis pigmentosa with rhodopsin mutations	scientific article	Retinal Function and Rhodopsin Levels in Autosomal Dominant Retinitis Pigmentosa With Rhodopsin Mutations

Statements

scholarly article

1 reference

Europe PubMed Central

4 August 2017

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

1 reference

Europe PubMed Central

4 August 2017

Retinal Function and Rhodopsin Levels in Autosomal Dominant Retinitis Pigmentosa With Rhodopsin Mutations (English)

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retinitis pigmentosa

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based on heuristic

inferred from title

4

object named as

Jeremy Nathans

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author name string

Jacobson SG

1

1 reference

Europe PubMed Central

4 August 2017

Kemp CM

2

1 reference

Europe PubMed Central

4 August 2017

Sung CH

3

1 reference

Europe PubMed Central

4 August 2017

Nathans J

4

1 reference

Europe PubMed Central

4 August 2017

Samuel G. Jacobson

1

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Colin M. Kemp

2

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Ching-Hwa Sung

3

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language of work or name

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publication date

1 September 1991

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Europe PubMed Central

4 August 2017

September 1991

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American Journal of Ophthalmology

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Europe PubMed Central

4 August 2017

112

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Europe PubMed Central

4 August 2017

256-271

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Europe PubMed Central

4 August 2017

3

1 reference

Europe PubMed Central

4 August 2017

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

Two forms of autosomal dominant primary retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

Cone-Rod Dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

Rhodopsin flash photolysis in man

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

Prolonged rod dark adaptation in retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

Absolute spectral sensitivity at different eccentricities

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

Rod and cone activity in patients with dominantly inherited retinitis pigmentosa: comparisons between psychophysical and electroretinographic measurements

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

Autosomal dominant retinitis pigmentosa. A method of classification

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

Visual function and rhodopsin levels in humans with vitamin A deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

Patterns of rod and cone dysfunction in Bardet-Biedl syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2976726-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0002-9394(14)76726-1

0 references

1 reference

Europe PubMed Central

4 August 2017

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