(Q70583502)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8442497%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

title

Visual prognosis in autosomal dominant optic atrophy (Kjer type) (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8442497%20AND%20SRC:MED&resulttype=core&format=json

autosomal dominant optic atrophy

12 October 2019

main subject

0 references

Kjer's optic neuropathy

1 reference

D Eliott

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8442497%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

E I Traboulsi

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8442497%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

I H Maumenee

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8442497%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

language of work or name

English

0 references

publication date

1 March 1993

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8442497%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Ophthalmology

12 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8442497%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

volume

115

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8442497%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8442497%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

page(s)

360-367

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8442497%20AND%20SRC:MED&resulttype=core&format=json

Dominant optic atrophy. The clinical profile

12 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2973589-5

Autosomal dominant optic atrophy. A spectrum of disability.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2973589-5

Hereditary optic atrophy with dominant transmission; three Danish families.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2973589-5

HEREDITARY OPTIC ATROPHY WITH DOMINANT TRANSMISSION AND EARLY ONSET

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2973589-5

Dominant hereditary optic atrophy with bitemporal field defects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2973589-5

A family with the dominant infantile form of optical atrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2973589-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2973589-5

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0002-9394(14)73589-5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8442497%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

1 reference