(Q35762534)

10 August 2017

0 references

Short wavelength-automated perimetry compared with standard achromatic perimetry in autosomal dominant optic atrophy (English)

1 reference

autosomal dominant optic atrophy

10 August 2017

main subject

0 references

author name string

J W Walters

series ordinal

1

1 reference

10 August 2017

A Gaume

series ordinal

2

1 reference

10 August 2017

L Pate

series ordinal

3

1 reference

10 August 2017

language of work or name

English

0 references

publication date

12 July 2006

1 reference

British Journal of Ophthalmology

10 August 2017

published in

1 reference

10 August 2017

volume

90

1 reference

10 August 2017

issue

10

1 reference

10 August 2017

page(s)

1267-1270

1 reference

Infantile optic atrophy with dominant mode of inheritance: a clinical and genetic study of 19 Danish families

10 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857431

The phenotype of normal tension glaucoma patients with and without OPA1 polymorphisms

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857431

Is normal tension glaucoma actually an unrecognized hereditary optic neuropathy? New evidence from genetic analysis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857431

Investigating the association between OPA1 polymorphisms and glaucoma: comparison between normal tension and high tension primary open angle glaucoma

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857431

A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857431

Diagnostic criteria in cominantly inherited juvenile optic atrophy. A report of three new families

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857431

Dominant optic atrophy: correlation between clinical and molecular genetic studies.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857431

Investigation of the association between OPA1 polymorphisms and normal-tension glaucoma in Korea

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1857431

An Autosomal Dominant Form of Low-Tension Glaucoma

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16837542

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Hereditary optic neuropathies

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16837542

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/BJO.2006.097196

1 reference

10 August 2017

1 reference

10 August 2017

1 reference