Relative afferent pupillary defects in patients with Leber hereditary optic neuropathy and unilateral visual loss (Q57785024)

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3 December 2019

title

Relative afferent pupillary defects in patients with Leber hereditary optic neuropathy and unilateral visual loss (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9727524%20AND%20SRC:MED&resulttype=core&format=json

Leber hereditary optic neuropathy

3 December 2019

main subject

1 reference

2

1 reference

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3 December 2019

author name string

D M Jacobson

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9727524%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

N R Miller

3

1 reference

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3 December 2019

S C Pollock

4

1 reference

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3 December 2019

W A Fletcher

5

1 reference

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3 December 2019

P J McNussen

6

1 reference

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3 December 2019

T J Martin

7

1 reference

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3 December 2019

language of work or name

English

0 references

publication date

1 August 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9727524%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Ophthalmology

3 December 2019

published in

1 reference

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3 December 2019

volume

126

1 reference

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3 December 2019

issue

2

1 reference

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3 December 2019

page(s)

291-295

1 reference

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Leber's hereditary optic neuropathy. Clinical manifestations of the 3460 mutation

3 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2898%2900152-4

Leber's hereditary optic neuropathy. Clinical manifestations of the 14484 mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2898%2900152-4

The early phase in Leber hereditary optic atrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2898%2900152-4

Ophthalmoscopic findings in Leber's hereditary optic neuropathy. II. The fundus findings in the affected family members

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2898%2900152-4

Fundus findings in Leber's hereditary optic neuroretinopathy. III. Fluorescein angiographic studies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2898%2900152-4

Ophthalmologic findings in Leber hereditary optic neuropathy, with special reference to mtDNA mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2898%2900152-4

Mastocytosis-induced nyctalopia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2898%2900152-4

Evidence for preserved direct pupillary light response in Leber's hereditary optic neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2898%2900152-4

Pupillary Escape in Disease of the Retina or Optic Nerve

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2898%2900152-4

The relationship between visual acuity, pupillary defect, and visual field loss

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2898%2900152-4

The relationship between static perimetry and the relative afferent pupillary defect

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2898%2900152-4

How to measure the relative afferent pupillary defect

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2898%2900152-4

Association of the 11778 mitochondrial DNA mutation and demyelinating disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2898%2900152-4

Leber hereditary optic neuropathy. Electron microscopy and molecular genetic analysis of a case

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2898%2900152-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2898%2900152-4

The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2898%2900152-4

inferred from DOI database lookup

7 January 2021

based on heuristic

Correlation of afferent pupillary defect with visual field loss on automated perimetry

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2898%2900152-4

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0002-9394(98)00152-4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9727524%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

1 reference