(Q37315772)

19 August 2017

Autosomal dominant cone-rod dystrophy with negative electroretinogram (English)

1 reference

19 August 2017

1 reference

Fujii N

1

1 reference

19 August 2017

Shiono T

2

1 reference

19 August 2017

Wada Y

3

1 reference

19 August 2017

Nakazawa M

4

1 reference

19 August 2017

Tamai M

5

1 reference

19 August 2017

Yamada N

6

1 reference

19 August 2017

language of work or name

English

0 references

publication date

1 October 1995

1 reference

British Journal of Ophthalmology

19 August 2017

1 reference

19 August 2017

79

1 reference

19 August 2017

10

1 reference

19 August 2017

916-921

1 reference

Cone dystrophies with negative photopic electroretinogram

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=505293

A novel mutation (Asn244Lys) in the peripherin/RDS gene causing autosomal dominant retinitis pigmentosa associated with bull's-eye maculopathy detected by nonradioisotopic SSCP

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=505293

Juvenile Batten's disease: an ophthalmological assessment of 26 patients

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=505293

The dark choroid in posterior retinal dystrophies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=505293

Chloroquine retinopathy. Evaluation by fluorescein fundus angiography

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=505293

Abnormal Findings in Relatives of Patients with Juvenile Hereditary Macular Degeneration (Stargardt’s Disease)

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=505293

Evolution of benign concentric annular macular dystrophy.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=505293

Congenital stationary night blindness with negative electroretinogram. A new classification

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=505293

Negative electroretinograms in retinitis pigmentosa.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=505293

Benign concentric annular macular dystrophy

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=505293

Bull's-eye maculopathy and negative electroretinogram

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=505293

Dominant Macular Degenerations the Cone Dystrophies

2 September 2018

1 reference

12 December 2020

Macular lesions associated with retinitis pigmentosa

1 reference

12 December 2020

Psychophysical and electroretinographic findings in X-linked juvenile retinoschisis

1 reference

12 December 2020

Bull's-eye maculopathy, negative electroretinogram and low plasma cyclic guanosine monophosphate level. A report of two cases

1 reference

12 December 2020

Identifiers

DOI

10.1136/BJO.79.10.916

1 reference

19 August 2017

1 reference

19 August 2017

PubMed publication ID

7488580

1 reference