(Q50606760)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7422264%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

title

Autosomal dominant optic atrophy. A spectrum of disability (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7422264%20AND%20SRC:MED&resulttype=core&format=json

autosomal dominant optic atrophy

18 October 2019

main subject

0 references

author name string

C S Hoyt

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7422264%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

publication date

1 March 1980

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7422264%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7422264%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

volume

87

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7422264%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7422264%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

page(s)

245-251

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7422264%20AND%20SRC:MED&resulttype=core&format=json

LEBER'S DISEASE IN THE NETHERLANDS.

18 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935247-0

7 January 2021

HEREDITARY OPTIC ATROPHY WITH DOMINANT TRANSMISSION AND EARLY ONSET

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935247-0

7 January 2021

Dominantly inherited optic atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935247-0

7 January 2021

Dominant hereditary optic atrophy with bitemporal field defects

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935247-0

7 January 2021

A family with the dominant infantile form of optical atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935247-0

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935247-0

7 January 2021

Four families with the dominant infantile form of optic nerve atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935247-0

7 January 2021

Hereditary optic atrophy with dominant transmission; three Danish families.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935247-0

7 January 2021

Dominant juvenile optic atrophy. A study in two families and review of hereditary disease in childhood

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935247-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935247-0

7 January 2021

The assessment of acquired dyschromatopsia and clinical investigation of the acquired tritan defect in dominantly inherited juvenile atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935247-0

7 January 2021

Dominant optic atrophy. The clinical profile

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935247-0

7 January 2021

Juvenile Diabetes Mellitus and Optic Atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935247-0

7 January 2021

10.1016/S0161-6420(80)35247-0

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7422264%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

1 reference