Prognostication in Stargardt Disease Using Fundus Autofluorescence: Improving Patient Care-Reference-Cited by-同舟云学术

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Prognostication in Stargardt Disease Using Fundus Autofluorescence: Improving Patient Care

Published:2023-11 Issue:11 Volume:130 Page:1182-1190
ISSN:0161-6420
Container-title:Ophthalmology
language:en
Short-container-title:Ophthalmology

Author:

Daich Varela Malena^ORCID,Laich Yannik^ORCID,Hashem Shaima Awadh,Mahroo Omar A.,Webster Andrew R.,Michaelides Michel

Funder

NIHR Biomedical Research Centre, Royal Marsden NHS Foundation Trust/Institute of Cancer Research

UCL Institute of Ophthalmology, University College London

Wellcome Trust

Moorfields Eye Hospital NHS Foundation Trust

Publisher

Elsevier BV

Subject

Ophthalmology

Reference43 articles.

1. Macular dystrophies: clinical and imaging features, molecular genetics and therapeutic options;Rahman;Br J Ophthalmol,2020

2. Genetic basis of inherited retinal disease in a molecularly characterized cohort of more than 3000 families from the United Kingdom;Pontikos;Ophthalmology,2020

3. Worldwide carrier frequency and genetic prevalence of autosomal recessive inherited retinal diseases;Hanany;Proc Natl Acad Sci U S A,2020

4. Über familiäre, progressive Degeneration in der Maculagegend des Auges;Stargardt;Albr von Graefes Arch für Ophthalmol,1909

5. Personalized genetic counseling for Stargardt disease: offspring risk estimates based on variant severity;Cornelis;Am J Hum Genet,2022

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic and Clinical Features of ABCA4-Associated Retinopathy in a Japanese Nationwide Cohort;American Journal of Ophthalmology;2024-08

2. Genotype-phenotype severity correlation in a multicentric portuguese cohort of ABCA4-associated retinopathy;AJO International;2024-07

3. Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes;Progress in Retinal and Eye Research;2024-05

4. Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom;2024-03-28

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