Macular function and morphologic features in juvenile stargardt disease: longitudinal study. (Q34615627)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25097154%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

title

Macular function and morphologic features in juvenile stargardt disease: longitudinal study (English)

1 reference

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12 March 2020

1 reference

1

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12 March 2020

Valentina Di Iorio

3

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12 March 2020

Francesca Simonelli

7

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12 March 2020

author name string

Paolo Melillo

2

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12 March 2020

Ada Orrico

4

1 reference

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12 March 2020

Marcella Attanasio

5

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12 March 2020

Settimio Rossi

6

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12 March 2020

publication date

2 August 2014

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12 March 2020

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12 March 2020

volume

121

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12 March 2020

page(s)

2399-2405

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12 March 2020

issue

12

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Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease.

12 March 2020

cites work

1 reference

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Clinical phenotypes and prognostic full-field electroretinographic findings in Stargardt disease

7 July 2018

1 reference

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Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy

7 July 2018

1 reference

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Macular function in macular degenerations: repeatability of microperimetry as a potential outcome measure for ABCA4-associated retinopathy trials

7 July 2018

1 reference

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Preferred retinal locus in macular disease: characteristics and clinical implications

7 July 2018

1 reference

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Comparison of ultrahigh- and standard-resolution optical coherence tomography for imaging macular pathology

7 July 2018

1 reference

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Electroretinographic findings in patients with Stargardt disease and fundus flavimaculatus

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4252720

Mechanistic studies of ABCR, the ABC transporter in photoreceptor outer segments responsible for autosomal recessive Stargardt disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4252720

Long-term follow-up of Stargardt's disease and fundus flavimaculatus

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4252720

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4252720

Evaluation of phenotypic similarities between Stargardt flavimaculatus and retinal pigment epithelial pattern dystrophies.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4252720

Models for longitudinal data: a generalized estimating equation approach

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4252720

Intrasession repeatability of fixation stability assessment with the Nidek MP-1.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4252720

Macular function assessed by microperimetry in patients with enhanced S-cone syndrome.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4252720

Imaging of the retinal pigment epithelium in age-related macular degeneration using polarization-sensitive optical coherence tomography.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4252720

Pattern electroretinography of larger stimulus field size and spectral-domain optical coherence tomography in patients with Stargardt disease

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4252720

Test-retest variability of microperimetry using the Nidek MP1 in patients with macular disease

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4252720

Evaluation of ranibizumab-induced changes in high-resolution optical coherence tomographic retinal morphology and their impact on visual function

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4252720

ISCEV Standard for full-field clinical electroretinography (2008 update).

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4252720

Three-dimensional spectral-domain optical coherence tomography images of the retina in the presence of epiretinal membranes

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4252720

Visual acuity loss and clinical observations in a large series of patients with Stargardt disease.

26 October 2018

1 reference

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Late-onset Stargardt disease is associated with missense mutations that map outside known functional regions of ABCR (ABCA4).

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4252720

A Longitudinal Study of Stargardt Disease: Clinical and Electrophysiologic Assessment, Progression, and Genotype Correlations

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4252720

Comparison of visual acuity loss in patients with different stages of Stargardt's disease

26 October 2018

1 reference

12 December 2020

Nidek MP1 is able to detect subtle decline in function in inherited and age-related atrophic macular disease with stable visual acuity

1 reference

12 December 2020

Phenotypic Subtypes of Stargardt Macular Dystrophy–Fundus Flavimaculatus

1 reference

12 December 2020

CLINICAL PHENOTYPE AS A PROGNOSTIC FACTOR IN STARGARDT DISEASE

1 reference

12 December 2020

Visual acuity loss in patients with Stargardt's macular dystrophy

1 reference

12 December 2020

Intrafamilial variation of phenotype in Stargardt macular dystrophy-Fundus flavimaculatus

1 reference

12 December 2020

1 reference

12 December 2020

10.1016/J.OPHTHA.2014.06.032

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25097154%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25097154%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

1 reference