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Ophthalmology, ISSN 0161-6420, 2016, Volume 123, Issue 6, pp. 1375 - 1385
Journal Article
Gene Therapy, ISSN 0969-7128, 10/2008, Volume 15, Issue 19, pp. 1311 - 1320
Journal Article
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, ISSN 0275-004X, 07/2019, Volume 39, Issue 7, pp. 1399 - 1409
Purpose: To investigate the natural history of Stargardt disease over a multiyear follow-up. Methods: We reviewed medical records of Stargardt disease... 
natural history study | optical coherence tomography | PHENOTYPE | ATROPHY SECONDARY | VISUAL-ACUITY LOSS | ELECTRORETINOGRAPHIC FINDINGS | AUTOFLUORESCENCE | FLECKS | electrophysiology | PROGSTAR | OPHTHALMOLOGY | Stargardt disease | ABCA4 gene | Macular degeneration | Development and progression | Genotype | Genetic aspects | Health aspects
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 6436 - 6436
Fundus autofluorescence (FAF) imaging is crucial to the diagnosis and monitoring of recessive Stargardt disease (STGD1). In a retrospective cohort study of 34... 
VISUALIZATION | MACULAR PIGMENT | SHORT-WAVELENGTH AUTOFLUORESCENCE | LIPOFUSCIN | FUNDUS AUTOFLUORESCENCE | MULTIDISCIPLINARY SCIENCES | NEAR-INFRARED AUTOFLUORESCENCE | STARGARDT DISEASE | FLUORESCEIN ANGIOGRAPHY | MELANIN | RETINAL-PIGMENT EPITHELIUM
Journal Article
Retina, ISSN 0275-004X, 02/2018, Volume 38, Issue 2, pp. 403 - 415
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 2016, Volume 57, Issue 13, pp. 5186 - 5191
Journal Article
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 2014, Volume 55, Issue 10, pp. 6139 - 6149
Journal Article
Journal Article
by Carss, Keren J and Carss, Keren and Arno, Gavin and Erwood, Marie and Stephens, Jonathan and Sanchis-Juan, Alba and Hull, Sarah and Megy, Karyn and Grozeva, Detelina and Dewhurst, Eleanor and Malka, Samantha and Plagnol, Vincent and Penkett, Christopher J and Penkett, Christopher and Stirrups, Kathleen and Rizzo, Roberta and Wright, Genevieve and Josifova, Dragana and Bitner-Glindzicz, Maria and Scott, Richard H and Scott, Richard and Clement, Emma and Allen, Hana Lango and Allen, Louise and Armstrong, Ruth and Brady, Angela F and Brady, Angie and Carmichael, Jenny and Chitre, Manali and Henderson, Robert H.H and Henderson, Robert and Hurst, Jane and MacLaren, Robert E and MacLaren, Robert and Murphy, Elaine and Paterson, Joan and Rosser, Elisabeth and Thompson, Dorothy A and Thompson, Dorothy and Wakeling, Emma and Ouwehand, Willem H and Michaelides, Michel and Moore, Anthony and Moore, Anthony T and Aitman, Timothy and Alachkar, Hana and Ali, Sonia and Allsup, David and Ambegaonkar, Gautum and Anderson, Julie and Antrobus, Richard and Arumugakani, Gururaj and Ashford, Sofie and Astle, William and Attwood, Antony and Austin, Steve and Bacchelli, Chiara and Bakchoul, Tamam and Bariana, Tadbir K and Baxendale, Helen and Bennett, David and Bethune, Claire and Bibi, Shahnaz and Bleda, Marta and Boggard, Harm and Bolton-Maggs, Paula and Booth, Claire and Bradley, John R and Brown, Matthew and Browning, Michael and Bryson, Christine and Burns, Siobhan and Calleja, Paul and Canham, Natalie and Caulfield, Mark and Chalmers, Elizabeth and Chandra, Anita and Chinnery, Patrick and Church, Colin and Clements-Brod, Naomi and Clowes, Virginia and Coghlan, Gerry and Collins, Peter and Cooper, Nichola and Creaser-Myers, Amanda and DaCosta, Rosa and Daugherty, Louise and Davies, Sophie and Davis, John and De Vries, Minka and Deegan, Patrick and Deevi, Sri V.V and Deshpande, Charu and Devlin, Lisa and Doffinger, Rainer and Dormand, Natalie and Drewe, Elizabeth and Edgar, David and Egner, William and Erber, Wendy N and ... and NIHR-BioResource Rare Dis and NIHR-BioResource Rare Diseases Consortium
The American Journal of Human Genetics, ISSN 0002-9297, 01/2017, Volume 100, Issue 1, pp. 75 - 90
Journal Article