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Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 03/2012, Volume 53, Issue 3, pp. 1264 - 1270
PURPOSE. To analyze reticular pseudodrusen progression using spectral domain-optical coherence tomography (SD-OCT). METHODS. Thirty-three consecutive patients... 
OPHTHALMOLOGY | PREVALENCE | FUNDUS FLAVIMACULATUS | IN-VIVO | Prognosis | Follow-Up Studies | Humans | Risk Factors | Male | Tomography, Optical Coherence - methods | Disease Progression | Retinal Drusen - diagnosis | Aged, 80 and over | Female | Aged | Retrospective Studies | Macula Lutea - pathology | Index Medicus
Journal Article
Revista Mexicana de Oftalmologia, ISSN 0187-4519, 03/2016, Volume 90, Issue 2, pp. 84 - 88
We report 4 cases of Stargardt disease/fundus flavimaculatus and we expose some considerations about the diagnosis and evolution of this retinal dystrophy.... 
Fundus flavimaculatus | Optical coherence tomography | Stargardt disease
Journal Article
Retina (Philadelphia, Pa.), ISSN 0275-004X, 12/2018, Volume 38, Issue 12, pp. 2387 - 2394
Purpose: To better define visual acuity loss in patients with Stargardt disease later in life. Methods: The most recent best-corrected visual acuities in the... 
ALLELES | FUNDUS FLAVIMACULATUS | ABCA4 | visual acuity | PHENOTYPES | FEATURES | GENE | DYSTROPHY | ABCA4 DISEASE | OPHTHALMOLOGY | COHORT | Stargardt disease | MUTATIONS | PROGRESSION | Macular degeneration | Visual acuity | Care and treatment | Research
Journal Article
Molecular Vision, ISSN 1090-0535, 02/2018, Volume 24, pp. 105 - 114
Purpose: To describe the retinal clinical features of a group of Mexican patients with Stargardt disease carrying the uncommon p.Ala1773Val founder mutation in... 
CONE-ROD DYSTROPHY | STARGARDT MACULAR DYSTROPHY | DEGENERATIONS | FUNDUS FLAVIMACULATUS | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSPORTER GENE ABCR | DISEASE | SEQUENCE VARIATIONS | OPHTHALMOLOGY | AUTOSOMAL RECESSIVE CONE | RETINITIS-PIGMENTOSA | PROGRESSION
Journal Article
Scientific Reports, ISSN 2045-2322, 10/2016, Volume 6, Issue 1, pp. 35414 - 35414
Stargardt disease (STGD1) is a juvenile macular degeneration predominantly inherited in an autosomal recessive pattern, characterized by decreased central... 
TRANSPORT | PROTEIN | DYSTROPHY | MULTIDISCIPLINARY SCIENCES | FUNDUS-FLAVIMACULATUS | PHENOTYPE | MACULAR DEGENERATION | RETINOPATHY | SYSTEMS | SPECTRUM | HISTOPATHOLOGY | Macular degeneration | Genetic counseling | Cell death | Exons | Genetic analysis | Retinal degeneration | Retina | Degeneration | Mutation | Dystrophy | Epithelium | Retinal pigment epithelium | Index Medicus
Journal Article
Journal Article
Journal Article
Ophthalmology, ISSN 0161-6420, 05/2018, Volume 125, Issue 5, pp. 735 - 746
Purpose: To describe the earliest features of ABCA4-associated retinopathy. Design: Case series. Participants: Children with a clinical and molecular diagnosis... 
GENE | EXTERNAL LIMITING MEMBRANE | DYSTROPHY | CONES | FUNDUS FLAVIMACULATUS | ROD | ONSET STARGARDT DISEASE | OPHTHALMOLOGY | RETINA | ERG | PIGMENT | Macular degeneration | Physiological aspects
Journal Article
Journal Article