Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q73939430)
Watch
English
Differential diagnosis of hereditary pigmentary maculopathies
scientific article published on 01 March 2000
In more languages
default for all languages
No label defined
No description defined
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10874200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10874200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
title
Differential diagnosis of hereditary pigmentary maculopathies
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10874200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10874200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
author name string
Reed KK
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10874200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10874200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
publication date
1 March 2000
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10874200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10874200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
published in
Clinical eye and vision care
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10874200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10874200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
volume
12
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10874200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10874200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
issue
1-2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10874200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10874200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
page(s)
3-14
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10874200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10874200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
cites work
The cone dystrophies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal cone synapses in human cone-rod dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cone and rod function in cone degenerations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Psychophysical evidence for more than two kinds of cone in dichromatic color blindness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Foveal cone mosaic and visual pigment density in dichromats
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The density of cones in the fovea centralis of the human dichromat.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Eye movement abnormalities in rod monochromatism and blue-cone monochromatism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial macular cone dystrophy: diagnostic value of multifocal ERG and two-color threshold perimetry
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Yearly rates of rod and cone functional loss in retinitis pigmentosa and cone-rod dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Retinitis pigmentosa inversa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Histopathology of bone spicule pigmentation in retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cone and rod ERGs in degenerations of central retina
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dominantly inherited drusen represent more than one disorder: a historical review
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assessment of the phenotypic range seen in Doyne honeycomb retinal dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adult vitelliform macular detachment occurring in patients with basal laminar drusen
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Refined genetic and physical positioning of the gene for Doyne honeycomb retinal dystrophy (DHRD)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Early findings in central areolar choroidal dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The development of central areolar choroidal dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fine localisation of the gene for central areolar choroidal dystrophy on chromosome 17p.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localisation of a gene for central areolar choroidal dystrophy to chromosome 17p.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Full-field electroretinograms in patients with central areolar choroidal dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Electroretinograms and pattern visually evoked cortical potentials in central areolar choroidal dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pattern dystrophies of the retinal pigment epithelium. The study of three generations in a family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pattern dystrophies of the retinal pigment epithelium.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pattern Dystrophy of the Retinal Pigment Epithelium
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Patterned anomalies of the retinal pigment epithelium: dystrophy or syndrome?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Vitelliform dystrophy and pattern dystrophy of the retinal pigment epithelium: concomitant presence in a family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Vitelliform dystrophy: long-term observations on New Zealand pedigrees
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Variable phenotypic expressivity of Best's vitelliform dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0953-4431%2899%2900042-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0953-4431(99)00042-9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10874200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10874200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
PubMed publication ID
10874200
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10874200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10874200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit