(Q44224593)

1 December 2017

X-linked progressive cone dystrophy. Clinical characteristics of affected males and female carriers (English)

1 reference

1 December 2017

Jacobson DM

1

1 reference

PubMed ID

2740082

1 December 2017

Thompson HS

series ordinal

2

1 reference

PubMed ID

2740082

1 December 2017

Bartley JA

series ordinal

3

1 reference

1 December 2017

1 June 1989

1 reference

1 December 2017

1 reference

1 December 2017

96

1 reference

1 December 2017

6

1 reference

1 December 2017

885-895

1 reference

CONE DYSFUNCTION SYNDROMES

1 December 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

X-linked recessive cone dystrophy with tapetal-like sheen. A newly recognized entity with Mizuo-Nakamura phenomenon

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

The cone degenerations

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Peripheral cone disease

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Progressive cone-rod degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Telangiectasia and Optic Atrophy in Cone-Rod Degenerations

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Dominant Macular Degenerations the Cone Dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Cone Dystrophy with Dominant Inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Progressive Generalized Cone Dysfunction

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Progressive cone dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

A new assessment of the normal ranges of the Farnsworth-Munsell 100-hue test scores

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Nomograms for the assessment of Farnsworth-Munsell 100-hue test scores

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Pupillary constriction to darkness

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Visual evoked potential and pupillary signs. A comparison in optic nerve disease

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

The photostress recovery test in the clinical assessment of visual function

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Further studies on acquired deficiency of color discrimination

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Acquired dyschromatopsias

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Congenital X-linked incomplete achromatopsia. Evidence for slow progression, carrier fundus findings, and possible genetic linkage with glucose-6-phosphate dehydrogenase locus

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Central areolar choroidal sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Hereditary Macular Degeneration and Amino-Aciduria

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

A new dominant progressive foveal dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Basic principles of clinical electroretinography

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Supernormal scotopic ERG in cone dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Cone dystrophy, nyctalopia, and supernormal rod responses. A new retinal degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Dominant progressive cone-rod dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Visual field changes in cone-rod degenerations

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Loss of electroretinographic oscillatory potentials, optic atrophy, and dysplasia in congenital stationary night blindness

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

Nerve fibre layer loss in diseases of the outer retinal layer

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2889%2932808-9

7 January 2021

10.1016/S0161-6420(89)32808-9

Identifiers

DOI

1 reference

1 December 2017

1 reference

PubMed ID

2740082