Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with Leber congenital Amaurosis type 2 (Q36906324)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23474247%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

title

Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with Leber congenital Amaurosis type 2 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23474247%20AND%20SRC:MED&resulttype=core&format=json

Leber congenital amaurosis

25 February 2020

main subject

congenital disorder

0 references

1 reference

1

1 reference

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25 February 2020

Eric A Pierce

4

1 reference

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25 February 2020

Sandro Banfi

7

1 reference

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25 February 2020

Enrico M. Surace

8

1 reference

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25 February 2020

Katherine A. High

13

1 reference

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25 February 2020

Alberto Auricchio

14

1 reference

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25 February 2020

Francesca Simonelli

16

1 reference

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25 February 2020

author name string

Albert M Maguire

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23474247%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Settimio Rossi

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23474247%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Paolo Melillo

5

1 reference

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25 February 2020

Kathleen Marshall

6

1 reference

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25 February 2020

Junwei Sun

9

1 reference

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25 February 2020

Carmela Acerra

10

1 reference

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25 February 2020

J Fraser Wright

11

1 reference

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25 February 2020

Jennifer Wellman

12

1 reference

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25 February 2020

Jean Bennett

15

1 reference

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25 February 2020

publication date

6 March 2013

1 reference

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25 February 2020

1 reference

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25 February 2020

volume

120

1 reference

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25 February 2020

page(s)

1283-1291

1 reference

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25 February 2020

issue

6

1 reference

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Pupillometric analysis for assessment of gene therapy in Leber Congenital Amaurosis patients

25 February 2020

cites work

1 reference

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AAV2 gene therapy readministration in three adults with congenital blindness.

29 September 2017

1 reference

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Gene therapy for leber congenital amaurosis caused by RPE65 mutations: safety and efficacy in 15 children and adults followed up to 3 years

29 September 2017

1 reference

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Leber congenital amaurosis due to RPE65 mutations and its treatment with gene therapy

29 September 2017

1 reference

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Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosa

29 September 2017

1 reference

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Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial

29 September 2017

1 reference

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Human RPE65 gene therapy for Leber congenital amaurosis: persistence of early visual improvements and safety at 1 year

29 September 2017

1 reference

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Treatment of leber congenital amaurosis due to RPE65 mutations by ocular subretinal injection of adeno-associated virus gene vector: short-term results of a phase I trial

29 September 2017

1 reference

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Leber congenital amaurosis: genes, proteins and disease mechanisms

29 September 2017

1 reference

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Effect of gene therapy on visual function in Leber's congenital amaurosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674112

Safety and efficacy of gene transfer for Leber's congenital amaurosis

29 September 2017

1 reference

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Clinical and molecular genetics of Leber's congenital amaurosis: a multicenter study of Italian patients

29 September 2017

1 reference

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Microperimetry and fundus autofluorescence in patients with early age-related macular degeneration.

29 September 2017

1 reference

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Ciliary neurotrophic factor (CNTF) for human retinal degeneration: phase I trial of CNTF delivered by encapsulated cell intraocular implants

29 September 2017

1 reference

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Lack of fundus autofluorescence to 488 nanometers from childhood on in patients with early-onset severe retinal dystrophy associated with mutations in RPE65.

29 September 2017

1 reference

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Properties of perimetric threshold estimates from Full Threshold, SITA Standard, and SITA Fast strategies.

29 September 2017

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29 September 2017

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ISCEV standard for clinical pattern electroretinography--2007 update

27 June 2018

1 reference

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Long-term follow-up of baseline learning and fatigue effects in the automated perimetry of glaucoma and ocular hypertensive patients

27 June 2018

1 reference

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

27 June 2018

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Computerized binocular pupillography of the swinging flashlight test detects afferent pupillary defects.

4 September 2018

1 reference

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Visual acuity as an outcome measure in clinical trials of retinal diseases

4 September 2018

1 reference

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The association between visual acuity and central retinal thickness in retinitis pigmentosa

4 September 2018

1 reference

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Fundus autofluorescence in children and teenagers with hereditary retinal diseases

4 September 2018

1 reference

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Variability of visual field measurements in normal subjects and patients with retinitis pigmentosa

4 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23474247

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23474247

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.OPHTHA.2012.11.048

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23474247%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23474247%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

1 reference