(Q40727742)

23 September 2017

A Clinicopathologic Study of Autosomal Dominant Optic Atrophy (English)

1 reference

https://api.crossref.org/works/10.1016/0002-9394(79)90565-8

autosomal dominant optic atrophy

11 March 2023

main subject

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1 reference

https://api.crossref.org/works/10.1016/0002-9394(79)90565-8

11 March 2023

V C Smith

3

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author name string

P. B. Johnston

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A315716

11 March 2023

R. N. Gaster

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A315716

11 March 2023

R. C. Tripathi

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A315716

11 March 2023

language of work or name

English

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publication date

1 November 1979

1 reference

full work available at URL

23 September 2017

https://api.elsevier.com/content/article/PII:0002939479905658?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0002-9394(79)90565-8

https://api.elsevier.com/content/article/PII:0002939479905658?httpAccept=text/plain

11 March 2023

1 reference

https://api.crossref.org/works/10.1016/0002-9394(79)90565-8

American Journal of Ophthalmology

11 March 2023

published in

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23 September 2017

88

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23 September 2017

5

1 reference

23 September 2017

868-875

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HEREDITARY OPTIC ATROPHY WITH DOMINANT TRANSMISSION AND EARLY ONSET

23 September 2017

3

1 reference

https://api.crossref.org/works/10.1016/0002-9394(79)90565-8

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

11 March 2023

7

1 reference

https://api.crossref.org/works/10.1016/0002-9394(79)90565-8

11 March 2023

8

1 reference

https://api.crossref.org/works/10.1016/0002-9394(79)90565-8

Four families with the dominant infantile form of optic nerve atrophy

11 March 2023

15

1 reference

https://api.crossref.org/works/10.1016/0002-9394(79)90565-8

A family with the dominant infantile form of optical atrophy

11 March 2023

16

1 reference

https://api.crossref.org/works/10.1016/0002-9394(79)90565-8

Dominantly inherited optic atrophy

11 March 2023

17

1 reference

https://api.crossref.org/works/10.1016/0002-9394(79)90565-8

LEBER'S DISEASE WITH SYMPTOMS RESEMBLING DISSEMINATED SCLEROSIS

11 March 2023

18

1 reference

https://api.crossref.org/works/10.1016/0002-9394(79)90565-8

Leber's hereditary optic atrophy: some clinical and aetiological considerations.

11 March 2023

19

1 reference

https://api.crossref.org/works/10.1016/0002-9394(79)90565-8

Neurological studies in families with Leber's optic atrophy

11 March 2023

20

1 reference

https://api.crossref.org/works/10.1016/0002-9394(79)90565-8

A family with sex linked optic atrophy : Ophthalmological and neurological aspects

11 March 2023

21

1 reference

https://api.crossref.org/works/10.1016/0002-9394(79)90565-8

11 March 2023

Identifiers

0 references

1 reference